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Auswahl der wissenschaftlichen Literatur zum Thema „Parent satisfaction with child care services“
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Zeitschriftenartikel zum Thema "Parent satisfaction with child care services"
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Mazhar, Mahpara, Faisal Rashid Khan, Asad Tamizuddin Nizami und Sadia Yasir. „Assessment of parent/ caretaker satisfaction with child and adolescent mental health services in a tertiary care setting“. Journal of Rawalpindi Medical College 25, Nr. 2 (30.06.2021): 152–58. http://dx.doi.org/10.37939/jrmc.v25i2.1217.
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BACKGROUND: Assessment of parent/caretaker satisfaction with child and adolescent mental health services in a tertiary care setting
METHODS: In this descriptive cross sectional study, 130 parents/caretakers of children aged ≤ 16 years were administered Parent/Caretaker Satisfaction Questionnaire which is a 20-item, 4-point Likert type scale, after their second visit/consultation with Child Psychiatric OPD via non-probability consecutive sampling directly as well as telephonically during six months period. Demographic variables were collected via Proforma. The data was analyzed using SPSS v 16.0. p- value <0.05 was considered significant.
RESULTS: 73.1% (n=95) were very satisfied (satisfaction level>60), 24.6 %(n=32) were satisfied (satisfaction between 21-60) and only 2.3%(n=3) were unsatisfied (satisfaction ≤20). No significant association was found between demographic variables and level of satisfaction.
CONCLUSION: Our study revealed a high level of parent/caretaker satisfaction with Child and Adolescent mental health services in a tertiary care setting. No significant association was found between socio-demographic variables and parent/caretakers’ satisfaction.
KEY WORDS: Patient satisfaction, Quality of health care, Child Psychiatry, Mental health services
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Conner, Jeanette M., und Eugene C. Nelson. „Neonatal Intensive Care: Satisfaction Measured From a Parent's Perspective“. Pediatrics 103, Supplement_E1 (01.01.1999): 336–49. http://dx.doi.org/10.1542/peds.103.se1.336.
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Health care systems today are complex, technically proficient, competitive, and market-driven. One outcome of this environment is the recent phenomenon in the health care field of “consumerism.” Strong emphasis is placed on customer service, with organized efforts to understand, measure, and meet the needs of customers served. The purpose of this article is to describe the current understanding and measurement of parent needs and expectations with neonatal intensive care services from the time the expectant parents enter the health care system for the birth through the discharge process and follow-up care. Through literature review, 11 dimensions of care were identified as important to parents whose infants received neonatal intensive care: assurance, caring, communication, consistent information, education, environment, follow-up care, pain management, participation, proximity, and support. Five parent satisfaction questionnaires—the Parent Feedback Questionnaire, Neonatal Index of Parent Satisfaction, Inpatient Parent Satisfaction–Children's Hospital Minneapolis, Picker Institute-Inpatient Neonatal Intensive Care Unit Survey, and the Neonatal Intensive Care Unit-Parent Satisfaction Form—are critically reviewed for their ability to measure parent satisfaction within the framework of the neonatal care delivery process. An immense gap was found in our understanding about what matters most and when to parents going through the neonatal intensive care experience. Additional research is required to develop comprehensive parent satisfaction surveys that measure parent perceptions of neonatal care within the framework of the care delivery process.
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Tuompo-Johansson, Erja, Fredrik Almqvist, Eeva Huikko und Ann-Christin Kairemo. „Child day care services and parents' satisfaction with them“. Nordic Journal of Psychiatry 52, Nr. 1 (Januar 1998): 51–59. http://dx.doi.org/10.1080/080394898422571.
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Christopher Amalraj Vallaba Doss, Syed Mohamed Sadath, Palanivel R M, Muhil Sakthivel, OLA Olatunji und Malik Khurram Shahzad Awan. „A Study on Parental Perception and Satisfaction towards Occupational Therapy Holistic Approach on Treatment and Service Delivery“. International Journal of Research in Pharmaceutical Sciences 11, Nr. 3 (22.07.2020): 3916–21. http://dx.doi.org/10.26452/ijrps.v11i3.2578.
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To highlight how holistic occupational therapy processes contribute to the level of parent’s perception and satisfaction, improve the therapist’s level of care, update therapist about client understands of their services, increase client’s awareness of different modes of occupational therapy treatment services. Quantitative descriptive cross-sectional study design, POC-20 Questionnaire is used to measure the processes of care questionnaire with parents ticking each column of items according to their perception and satisfaction. MPOC-20 question output from the interview results shows the treatment care services that enable parents to understand how the therapist takes effort and satisfied them day to day life. Therapist expressed their confidence in the holistic approachability to manage the child’s behaviors and act as the family center-point of contact for their ongoing care. This research clearly demonstrates the value of the holistic approach, parent and child place on receiving their service care close to home and how the therapist uses their holistic approach to enable this. The success of this study demonstrates this model of care can be implemented in other services across the world.
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Battalen, Adeline Wyman, Abbie E. Goldberg, David M. Brodzinsky, Ruth G. McRoy und Summer S. Hawkins. „Heterosexual and sexual minority adoptive parents’ help-seeking and service satisfaction of pediatricians and mental health providers“. Developmental Child Welfare 1, Nr. 3 (September 2019): 233–50. http://dx.doi.org/10.1177/2516103219873011.
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The aim of our study was to examine the associations between heterosexual and sexual minority adoptive parents’ adoption-related help-seeking and their service satisfaction with pediatricians and mental health providers. We examined associations with (a) satisfaction with pediatricians and (b) understanding of adoption by a mental health provider among adoptive parents who sought advice for adoption-related issues using data drawn from the Modern Adoptive Families study ( N = 1,419). Logistic regressions were used to examine associations with service-seeking and satisfaction with professionals’ adoption advice. About half of the sample adopted a child with either special needs at placement (55%) and/or preplacement adversity (74%), which were significantly associated with seeking adoption-related advice. Consulting pediatricians about adoption was common (78%), and 83% of those parents reported being satisfied with adoption-related advice provided by their pediatrician. About half (51%) of the parents sought mental health services, but only 41% of those parents reported having access to an adoption-competent mental health provider and 50% of those parents felt their mental health provider understood adoption. Parent sexual orientation, higher income, older child age, and having a child with special needs were positively associated with satisfaction with adoption-related advice provided by the pediatrician and having a mental health provider who understood adoption. Adopting a child with special needs at placement and an older child were positive associations of seeking adoption-related help, while parent demographics, including higher household income, were positively associated with satisfaction. Results suggest an inclusive family-centered approach to care is important.
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McIntyre, Laura Lee. „Parent Training for Young Children With Developmental Disabilities: Randomized Controlled Trial“. American Journal on Mental Retardation 113, Nr. 5 (01.09.2008): 356–68. http://dx.doi.org/10.1352/2008.113:356-368.
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Abstract A randomized controlled trial was used to evaluate a parent training intervention for caregivers with preschool-age children with developmental disabilities. The 21 families in the experimental group received usual care plus the 12-week Incredible Years Parent Training Program with developmental delay modifications. Families in the control group (n = 23) received usual care, including early childhood education and related services. Results suggest that this parent training intervention was superior to usual care for young children with developmental delays or disabilities in reducing negative parent–child interactions and child behavior problems. Participants in the experimental group indicated high satisfaction with treatment. Additional research is necessary to document maintenance and generalization of treatment outcomes.
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Ahmed, Riaz, Jamshed Akhtar, Naima Zamir, Syed Muhammad Raees Hussain Taqvi und Safia Bibi. „Assessment of Parental Satisfaction with Day-Care Surgical Services in a Tertiary Level Pediatric Hospital“. Annals of King Edward Medical University 28, Nr. 1 (30.04.2022): 7–12. http://dx.doi.org/10.21649/akemu.v28i1.5003.
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Background: Parental feedback is important for improving quality of the surgical services provided.Objective: This study was conducted to assess the level of satisfaction of parents with the day-care surgical services so as to find out where improvement is needed. Methods: This was an observational cross sectional study conducted in the Department of Pediatric Surgery, National Institute of Child Health, Jinnah Sindh Medical University Karachi from September 2019 to April 2020. The parents of the children who underwent different day-care surgical procedures were included. A validated Parent Satisfaction Scale (PSS) which consist of 11-items was used. The responses were made according to Likert scale. Three groups of satisfied, undecided and unsatisfied study participants were made according to the scores obtained. The socio-demographic variables including age of parents and children, level of education, and income group were compared amongst study groups. Results: Total of 114 parents participated. The most common procedure performed was inguinal herniotomy (n=59). Seven (6%) patients were brought back after discharge due to pain. Eighty-seven (76.30%) parents were satisfied with the services provided while 18 (15.8%) were unsatisfied and 9 (7.9%) undecided. A significant difference in the satisfaction level of the study participants noted with respect to the mean age of parents (p=0.039), level of education (p< 0.001) and income groups (p< 0.001). Conclusion: Majority of the study participants were satisfied with the surgical services provided. Lack of respect given by the hospital staff and delay in getting treatment were the main reasons for dissatisfaction. Socio-demographic characteristics of the study participants were significantly associated with the level of satisfaction.
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Feragen, Kristin Billaud, Tone Kristin Særvold, Ragnhild Aukner und Nicola Marie Stock. „Speech, Language, and Reading in 10-Year-Olds with Cleft: Associations with Teasing, Satisfaction with Speech, and Psychological Adjustment“. Cleft Palate-Craniofacial Journal 54, Nr. 2 (März 2017): 153–65. http://dx.doi.org/10.1597/14-242.
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Background Despite the use of multidisciplinary services, little research has addressed issues involved in the care of those with cleft lip and/or palate across disciplines. The aim was to investigate associations between speech, language, reading, and reports of teasing, subjective satisfaction with speech, and psychological adjustment. Design Cross-sectional data collected during routine, multidisciplinary assessments in a centralized treatment setting, including speech and language therapists and clinical psychologists. Participants Children with cleft with palatal involvement aged 10 years from three birth cohorts (N = 170) and their parents. Outcome Measures Speech: SVANTE-N. Language: Language 6-16 (sentence recall, serial recall, vocabulary, and phonological awareness). Reading: Word Chain Test and Reading Comprehension Test. Psychological measures: Strengths and Difficulties Questionnaire and extracts from the Satisfaction With Appearance Scale and Child Experience Questionnaire. Results Reading skills were associated with self- and parent-reported psychological adjustment in the child. Subjective satisfaction with speech was associated with psychological adjustment, while not being consistently associated with speech therapists’ assessments. Parent-reported teasing was found to be associated with lower levels of reading skills. Having a medical and/or psychological condition in addition to the cleft was found to affect speech, language, and reading significantly. Conclusions Cleft teams need to be aware of speech, language, and/or reading problems as potential indicators of psychological risk in children with cleft. This study highlights the importance of multiple reports (self, parent, and specialist) and a multidisciplinary approach to cleft care and research.
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Bradley, Caroline, Crispin Day, Caroline Penney und Daniel Michelson. „‘Every day is hard, being outside, but you have to do it for your child’: Mixed-methods formative evaluation of a peer-led parenting intervention for homeless families“. Clinical Child Psychology and Psychiatry 25, Nr. 4 (01.06.2020): 860–76. http://dx.doi.org/10.1177/1359104520926247.
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We conducted a mixed-methods, formative evaluation of a peer-led parenting intervention for homeless families. Participants were parents living in temporary accommodation with self-identified difficulties related to parenting an index child aged 2–11 years. An evidence-based programme (‘Empowering Parents, Empowering Communities’) was adapted for delivery with the target population in London, UK. We assessed feasibility in terms of session attendance rate, intervention completion rate and potential for impact on a range of parent-reported outcomes measures. Acceptability and appropriateness were examined by a user satisfaction measure and qualitative interviews. The intervention was delivered across three group cohorts ( N = 15). Thirteen parents completed the programme (including one parent who required two attempts). We found improvements in child behavioural difficulties, parenting knowledge and practices, while parental well-being and social support were unchanged. Participants were highly satisfied overall, with indications that the peer-led model mitigated negative expectancies of services and normalized experiences of parenting in challenging conditions. Parental self-care and ‘the good enough parent’ were strongly endorsed topics, although some content (e.g. timeout) was deemed impractical. These promising findings warrant further testing under controlled conditions.
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Vellingiri, Sutharshana. „Assessment of Parent's Preference to General or Local Anesthesia for Children undergoing Dental Treatment“. World Journal of Dentistry 6, Nr. 3 (2015): 154–60. http://dx.doi.org/10.5005/jp-journals-10015-1333.
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ABSTRACT Background Investigators have begun to address the relationship of parental satisfaction with dental care for children since the dentist/physician and the patient are all aware of the services being provided. These determining characters are essential for compliance of the patient, as patient satisfaction is directly related to health-related issues, needs, and practice. Patient satisfaction has an important role in determining the utilization of the healthcare services and the compliance behavior of the patients. Factors which can influence the patients’ decision to seek care and follow through to the completion of the treatment process can affect the physiologic and functional outcomes of the treatment. Hence, this survey was done to evaluate parent's preference to general or local anesthesia in their children's dental treatments. Materials and methods In this survey, a modified and adapted questionnaire from a previously tested survey that was used to assess parental satisfaction with dental treatments under general anesthesia in pediatric dentistry, was used to assess parents’ preference to general or local anesthesia. Parents whose children were going to undergo treatments in Department of Pedodontics, Saveetha Dental College, was issued with this questionnaire and clinical examination of teeth present and treatment to be done was examined. Results Ninety-seven percent of the parents preferred local anesthesia to general anesthesia. Parents preferred general anesthesia most only in case child below the age of 3 and when multiple settings are required of and their knowledge about anesthesia and its side effects was found to low and preferred local anesthesia in most cases. Conclusion Parents play a unique role in dental care and over all well being of the child. Some parents and dental practitioners prefer the presence of a parent with their child during the delivery of in-office dental care. Parents are aware of their child's previous dental experiences and are also aware of the child's interest and fear. Most of the parent's preference was to local anesthesia (97%) and preferred general anesthesia under given circumstances. How to cite this article Vellingiri S, Gurunathan D. Assessment of Parent's Preference to General or Local Anesthesia for Children undergoing Dental Treatment. World J Dent 2015;6(3):154-160.
Dissertationen zum Thema "Parent satisfaction with child care services"
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Elliott, Roslyn, University of Western Sydney, of Arts Education and Social Sciences College und School of Education and Early Childhood Studies. „The book is open but you can't turn the page: parents' perceptions of early childhood service quality“. THESIS_CAESS_EEC_Elliot_R.xml, 2003. http://handle.uws.edu.au:8081/1959.7/800.
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This research examines parents’ perceptions of quality on early childhood services as they support families in the care and education of children. Data were collected from parents of under school-aged children using interviews, questionnaires and focus groups. Data analysis has enabled a determination of: the link between parents’ perceptions of quality and early childhood professionals’ views as expressed in the literature; parents’ satisfaction with services and the evaluation processes used by them; opportunities available to parents to engage with service staff to influence the quality of the services provided; and parents’ knowledge and use of the information services provided by the National Childcare Accreditation Council to assist them in their decision making regarding early childhood services. Results showed that communication between parents and staff is problematic. An accretion model of communication is developed to enhance the quality of early childhood services by promoting shared understanding and values between parents and staff, enabling parents to take part in decision making and minimising perceptions of threat to staff’s professional integrityUniversity of Western Sydney
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Elliott, Roslyn. „The book is open but you can't turn the page: parents' perceptions of early childhood service quality“. Thesis, View thesis, 2003. http://handle.uws.edu.au:8081/1959.7/800.
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This research examines parents’ perceptions of quality on early childhood services as they support families in the care and education of children. Data were collected from parents of under school-aged children using interviews, questionnaires and focus groups. Data analysis has enabled a determination of: the link between parents’ perceptions of quality and early childhood professionals’ views as expressed in the literature; parents’ satisfaction with services and the evaluation processes used by them; opportunities available to parents to engage with service staff to influence the quality of the services provided; and parents’ knowledge and use of the information services provided by the National Childcare Accreditation Council to assist them in their decision making regarding early childhood services. Results showed that communication between parents and staff is problematic. An accretion model of communication is developed to enhance the quality of early childhood services by promoting shared understanding and values between parents and staff, enabling parents to take part in decision making and minimising perceptions of threat to staff’s professional integrity
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Clark, Nancy Elizabeth. „Perceptions of satisfaction in the delivery of services to kinship and non-kinship care providers“. CSUSB ScholarWorks, 2004. https://scholarworks.lib.csusb.edu/etd-project/2463.
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Kansteiner, Suzanne. „A parent handbook for family childcare programs“. [Denver, Colo.] : Regis University, 2007. http://165.236.235.140/lib/SKansteiner2007.pdf.
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Booth, Nicola. „Becoming a parent to an infant requiring neonatal intensive care“. Thesis, Liverpool John Moores University, 2011. http://researchonline.ljmu.ac.uk/6095/.
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The number of babies that require care in the Neonatal Intensive Care Unit continues to rise in the UK and parents who have a baby who is born sick or prematurely find themselves adapting to this stressful and often unexpected event whilst also trying to establish their role as a new parent. With no current large British studies, this study explores the experiences of both mothers and fathers in the NICU in relation to adaptation and parental role development and how their experience changes over time. In total 76 parents were interviewed using semi structured interviews 7-10 days following the birth to capture their early experiences of the NICU and then again beyond 28 days to explore any changes in their views and feelings over time. Interviews were tape recorded, transcribed verbatim into the written word and imported into WINMAX PRO. Data analysis revealed nine major sections. These are preparation prior to birth, labour and delivery, first sight of infant, support from the partner, family, friends and other parents, support from and communication with staff, adaptation to the NICU experience, development of the parental role, changes with time and the experiences of fathers. Findings show differences in what mothers and fathers find stressful about their NICU experience, how they adapt to the birth of a sick or premature infant and in their development of the parental role. With the passage of time the events surrounding the birth became less significant as parents start to look to the future. Their role as a parent continued to develop with feelings that their baby needed and recognised them, but many parents felt that they were unable to influence what happened to their baby in the NICU. Recommendations are made for further research and for changes to NICU practice.
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Martin, Lila Marie. „Foster parent satisfaction“. CSUSB ScholarWorks, 2004. https://scholarworks.lib.csusb.edu/etd-project/2567.
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The findings of this study offer agencies useful ways to develop social relationships with foster parents and to implement useful and accessible training opportunities. Strengthening what works well frees agencies to promote these areas to recruit new parents and simultaneously maintain quality foster homes.
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Packard, Anna Elise. „Parent Functioning and Child Psychotherapy Outcomes: Predicting Outcomes in Usual Care“. BYU ScholarsArchive, 2009. https://scholarsarchive.byu.edu/etd/2311.
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A prominent need in the youth psychotherapy literature includes the examination of mechanisms of change within the context of "real world" clinical settings, where the practice of psychotherapy differs significantly from that in controlled clinical trials. In examining mechanisms of change in youth psychotherapy, variables related to parent functioning may be among the most important factors to consider in predicting and promoting good child outcomes. The purpose of the present study was to evaluate three important aspects of parent functioning—psychological symptom distress, interpersonal relations, and social role performance—as potential predictors of successful treatment outcomes in a traditional community outpatient treatment setting for children and adolescents. Further, this study examined whether parents indirectly benefited from their children receiving services, expanding our view on the scope and benefits inherent in youth psychotherapy. Parent Symptom Distress, Interpersonal Relations, and Social Role performance were measured using the domains of the Outcome Questionnaire 45 (OQ-45; Lambert et al., 2004), and youth treatment outcomes were measured using the parent and self-report versions of the Youth-Outcome Questionnaire (Y-OQ; Burlingame, Wells, Lambert, & Cox, 2004; Y-OQ-SR; Wells, Burlingame & Rose, 2003). Using Hierarchical Linear Modeling with this sample of 339 youth, aged 4-17 and their parents, this study examined the relationship between these parent domains and youth progress in therapy. Results revealed that parent Symptom Distress and Social Role performance improved significantly over the course of youth treatment. Further, Social Role performance at intake significantly predicted the rate of change in parent-reported youth outcome; and Interpersonal Relations at intake significantly predicted rate of change in youth-reported outcome. Finally, changes in parent Social Role performance were associated with changes in youth symptoms over the course of treatment. Examining the associations between these variables is an important step toward identifying potential mechanisms of change in youth mental health treatment. The results of this study provide valuable information on the importance of attending to parent functioning in the assessment and treatment of youth mental health issues.
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Kim, Jung-Eun. „The Impact Of Child Care Center Partnerships with Head Start Agencies on Parents' Satisfaction with Child Care and Early Education“. Case Western Reserve University School of Graduate Studies / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=case1333497812.
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Albarran, Ruth Maria, und Ranee Taechameena Sahachartsiri. „Foster parent satisfaction and retention“. CSUSB ScholarWorks, 2008. https://scholarworks.lib.csusb.edu/etd-project/3399.
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This study proposed to explore several factors that promote foster parent satisfaction in order to preserve quality foster homes to serve the 532,000 displaced children currently in the child welfare system. A sample of 52 foster parents were surveyed to determine overall satisfaction with their foster care experience at Children's Way Foster Family Agency in San Bernardino, California. It was hypothesized that the higher the level of foster parent satisfaction, the higher rates of retention. A modified version of an existing instrument titled "Foster Parent Satisfaction Survey" was utilized in this study.
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Goedken, Amber Marie. „The impact of parental health coverage on insured children's utilization of health care services“. Diss., University of Iowa, 2011. https://ir.uiowa.edu/etd/2706.
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Over six million insured children belong to families where the parents in their household lack health insurance. Studies have indicated insured low-income children with uninsured parents are less likely to have physician visits and well-child visits than their counterparts with insured parents. However, self-selection may be responsible for the relationship found between parental insurance and well-child visits. No studies have been undertaken to examine the impact of parental insurance on the utilization of children with chronic conditions. Social Cognitive Theory was used to model children's health care utilization and explain the relationship between parental insurance and that utilization. The objectives of the study are to estimate the effect of health insurance for the primary parent on (1) insured children's well-child visits and (2) physician visits for asthma in insured children.
This study used a cross-sectional design. The data source was the 2007 Medical Expenditure Panel Survey-Household Component. The sample consisted of children 17 years or less who were insured through the same source(s) for the entire year and had a primary parent who was either insured or uninsured the entire year. The dependent variable for the entire sample was whether or not the child had at least one well-child visit during the year. The dependent variables for the subsample of children with asthma were (1) whether or not the child had at least one asthma-related physician visit and (2) whether or not the child had at least two asthma-related physician visits. The independent variables were the same for the three analyses and were selected to represent the Social Cognitive Theory determinants. These included parent (insurance, sex, worry, education, language, employment, health use, health, risk aversion, and self care expectation), child (source of coverage, age, health, race, and oldest child), and household (Metropolitan Statistical Area, region, number of children, number of parents, and income) variables. Probit and bivariate probit models were estimated for each dependent variable. The percentage of children with insured parents that had a well-child visit during the year was significantly higher than the percentage of children with uninsured parents that had a well-child visit (50.6% vs. 42.8%, respectively). However, multivariate analyses revealed no significant relationship between parental insurance and well-child visits. The percentages of children with insured and uninsured parents that had an asthma-related physician visit were 29.6% and 32.6%, respectively. The percentages that had at least two asthma-related visits were 14.9% and 14.6%, respectively. No significant relationship was found between parental insurance and asthma-related physician visits. The region of the United States where the child lived and whether the child's parent was employed were associated with each type of utilization. Other determinants were also associated with children's utilization, but these varied with the type of utilization. In conclusion, insured children with insured parents are no more likely to have a well-child or asthma-related physician visit during the year than insured children with uninsured parents.
Bücher zum Thema "Parent satisfaction with child care services"
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Bolland, Rachael. The worst parent in Britain: Proposals for reforms in institutionalised childcare. London: Bow Group, 2000.
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O'Hagan, Maureen. Special issues in child care. London: Baillière Tindall, 1993.
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Handwerger, Sharon. The minority female single parent demonstration: Child care referral options : a technical research report. New York: Rockefeller Foundation, 1990.
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Phillips, Nancy H. Choosing schools and child care options: Answering parents' questions. Springfield, Ill., U.S.A: C.C. Thomas, 1994.
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Handwerger, Sharon. The minority female, single parent demonstration: Program costs : a technical research report. New York: Rockefeller Foundation, 1990.
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Hollister, Robinson G. The minority female single parent demonstration: New evidence about effective training strategies. New York: Rockefeller Foundation, 1990.
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United, States Congress House Select Committee on Children Youth and Families. Families and child care: Improving the options : a report. Washington: U.S. G.P.O., 1985.
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United States. Congress. House. Select Committee on Children, Youth, and Families. Families and child care: Improving the options : a report. Washington: U.S. G.P.O., 1985.
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Kevin, Browne, Hrsg. A community health approach to the assessment of infants and their parents: The CARE programme. Chichester, England: John Wiley & Sons, 2006.
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From birth to one: The year of opportunity. Buckingham: Open University Press, 2002.
Den vollen Inhalt der Quelle findenBuchteile zum Thema "Parent satisfaction with child care services"
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Bucquois, P., und A. Francaux. „Effectiveness Analysis of Residential Child Care Services in Belgium“. In The State as Parent, 409–11. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-1053-9_33.
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Nielsen, Fran. „Art Therapy“. In Longer-Term Psychiatric Inpatient Care for Adolescents, 95–105. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-1950-3_11.
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AbstractThe use of group art therapy, individual art therapy and family art therapy in an inpatient child and adolescent mental health services unit will be described, including images and consumer feedback to demonstrate effectiveness. The artworks made in art therapy can reveal hidden dysfunction in the young person and/or their family members. Recent trauma research supports capacity to access this material safely through non-verbal visual communication. Family art therapy has been a useful intervention to support the identification of illness in a parent, to improving attunement between the parent and the child and for the parent to detach from their child’s symptoms by agreeing to get treatment for themselves. If the patient cannot separate from the illness in the parent, their symptoms will persist.
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Downe, Soo, Claudia Meier Magistretti, Shefaly Shorey und Bengt Lindström. „The Application of Salutogenesis in Birth, Neonatal, and Infant Care Settings“. In The Handbook of Salutogenesis, 465–77. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-79515-3_43.
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AbstractIn this chapter, the relation of salutogenesis to maternity care is discussed by giving a critical overview of studies in perinatal care, primarily measuring and promoting parental sense of coherence (SOC) and well-being.An overview is given on salutogenic approaches to neonatal and infant service provision. Important aspects of and salutogenic interventions for parent–child attachment in the first year of a child’s life are examined. Parents’ and caregivers’ relationship with their infants and newborns plays a critical role in shaping the emotional, cognitive, and social development of their child. Different interventions of early support to optimize parenting capacity and their impact are also discussed.Although the chapter focuses only on examples of salutogenic approaches based on reasonable evidence, there is a growing awareness of the value of salutogenic approaches to the provision of maternity care, and to facilities and services to enhance parenting and well-being in infancy and early childhood. Research gaps are identified, and suggestions for the direction of future research are outlined.
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Ali Samadi, Sayyed. „Online Training for Parents of Individuals with Autism Spectrum Disorders during COVID-19 Pandemic“. In Parenting - Challenges of Child Rearing in a Changing Society [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.102949.
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Caregiving for individuals with autism spectrum disorders (ASDs) during COVID-19 lockdown was a challenge for parents. Daycare centers were closed, and parents had to provide 24-hour caregiving. Parents and children spent more time together during the pandemic. This study aimed to understand the impacts of online systems as parental support and to comprehend the parental perception regarding this type of service. Eight weeks of training were provided for the volunteer daycare centers. The centers covered a sizable group of parents of children with ASD in different age levels. A mixed-method approach for data collection was considered to understand the impacting factors. Telecommunication facilities enable daycare service providers to continue their support from a distance by enabling parents to provide care for a longer period and in a wider range during the pandemic. Parental feedback after the training course was collected. A low dropout rate was reported. Parents, in general, were satisfied with the course. Different contributing factors contributed to this satisfaction. Results also indicate that the use of online parental support is a good choice for parents in emergencies and times of lockdown. To understand the advantage and shortcomings of online parents’ training services, further studies are needed.
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Katz, Sanford N. „Child Protection“. In Family Law in America, 177–204. Oxford University Press, 2021. http://dx.doi.org/10.1093/oso/9780197554319.003.0005.
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This chapter studies the parent–child relationship through the lens of child protection laws, with emphasis on the issues of state intervention into that relationship. Throughout the history of the laws governing the complex relationship of parent, child, and state, there has been a struggle between parental authority and family privacy, on the one hand, and the state's responsibility of guarding the best interests of the child, on the other. The rhetoric has been that parents have the basic right to raise their children as they see fit, subject to their not overstepping the bounds of reasonableness in all aspects of childrearing. However, parental rights are not unlimited. Historically, the state, the ultimate parent who looks after all the children in society under the parens patriae concept, has a right to subject parents to public scrutiny and legal examination. In the United States, in the main, child protection in the form of child welfare services in the latter part of the twentieth century and the beginning of the twenty-first is basically the responsibility of the states. State social service agencies under the executive branch deliver certain social services themselves but more commonly for reasons of economy contract for foster care and adoption services with private social service agencies, which they monitor. The chapter then looks at the federal government's impact on the child protection systems in the states.
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(Bo) Kennedy, Robert M. „Effective management of children’s pain and anxiety in the emergency department“. In Oxford Textbook of Paediatric Pain, 338–50. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642656.003.0034.
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Effective management of children’s pain and anxiety during emergency department (ED) visits facilitates medically necessary care and procedures and increases patient, family, and health care provider satisfaction. This chapter will review evidence-based techniques for achieving this goal. A significant focus is upon non-pharmacological strategies to relieve children’s anxiety because high levels of anxiety exacerbate sensitivity to pain and disrupt coping mechanisms of the child and parent. In addition, advances in techniques for pain relief for specific procedures will be detailed. Aspects of procedural sedation and analgesia that are especially pertinent to the ED will also be reviewed along with two recommended regimens for moderate and deep sedation.
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Walsh, Kathleen, Melissa Jonnson, Wallace Wong und Veronique Nguy. „IMPROVING THE ASSESSMENT OF CHILDREN AND YOUTH WHO PRESENT WITH GENDER DYSPHORIA: An investigation into patient and parent satisfaction“. In Advances in Psychology and Psychological Trends, 217–25. inScience Press, 2020. http://dx.doi.org/10.36315/2021pad20.
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Practitioners working with gender non-conforming children and youth ascribe to general guidelines based on the World Professional Association for Transgender Health Standards of Care for the Health of Transsexual, Transgender, and Gender Nonconforming People (2012). These guidelines inform clinical practice and assessment and emphasize the need for gender affirming care, but they do not include strict treatment criteria. Consequently, there are multiple perspectives and approaches in the field regarding effective assessment and treatment of gender diverse and transgender clients. Given the ongoing debate around best practices, the current exploratory research study investigates the perspectives and satisfaction of transgender youth and their parents actively seeking out gender health assessments (e.g., hormone readiness assessments). Twenty-five parents and 22 youth who were accessing gender health services through a community outpatient clinic completed a questionnaire about the gender health assessment process. Survey data was analyzed using descriptive statistics, and portions analyzed using thematic analysis. Similar responsepatterns were found between groups and themes emerged surrounding the need for an individualized approach to care. This study aims to increase clinical understanding of the experiences of those seeking gender health assessment services to inform and improve practices to better serve this community.
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James, Sigrid, und Juri Kilian. „Residential Care for Children and Youth in Germany“. In Revitalizing Residential Care for Children and Youth, 209—C15.P68. Oxford University Press, 2022. http://dx.doi.org/10.1093/oso/9780197644300.003.0015.
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Abstract This chapter notes the long historical tradition of residential care in Germany and its current expression in a wide variety of settings. Residential care programs mostly consist of small community-based group homes and supported living units with about seven to 10 youths and four or five pedagogical staff. Some homes offer specialized services (e.g., therapeutic residential care, wilderness programs, mother–child homes). The authors note that residential care is guided by general pedagogical principles and concepts, emphasizing learning through a milieu-based and “life-space-oriented” perspective (Lebensweltorientierung), which stresses an individualized, participatory, and relationship-based approach. Parent engagement and youth participation are also noted as important, as are the growing numbers of unaccompanied minors and their impact on the residential care system. The chapter concludes with the matrix used throughout the book, which provides information about the current policy context, key trends and initiatives, characteristics of children and youth served, preparation of residential care personnel, promising programmatic innovations, and present strengths and challenges.
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(Bo) Kennedy, Robert M. „Effective management of children’s pain and anxiety in the Emergency Department“. In Oxford Textbook of Pediatric Pain, herausgegeben von Bonnie J. Stevens, Gareth Hathway und William T. Zempsky, 361–72. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780198818762.003.0035.
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Effective management of children’s pain and anxiety during Emergency Department (ED) visits facilitates medically necessary care and procedures, and increases patient, family, and healthcare provider satisfaction. This chapter will review and update the chapter from the first edition that described evidence-based techniques for achieving this goal. A significant focus is on nonpharmacological strategies to relieve children’s anxiety, because high levels of anxiety exacerbate sensitivity to pain and disrupt the coping mechanisms of the child and parent. In addition, advances in techniques for pain relief for specific procedures will be detailed. Aspects of procedural sedation and analgesia that are especially pertinent to the ED will also be reviewed, along with two recommended regimens for moderate and deep sedation.
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Berk, Laura E. „The Child in Contemporary Culture“. In Awakening Children's Minds. Oxford University Press, 2001. http://dx.doi.org/10.1093/oso/9780195124859.003.0011.
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In this chapter, I take up dilemmas that today’s parents face in rearing young children. Throughout this book, we have touched on myriad forces that make contemporary parenting highly challenging. These include one-sided, contradictory messages in the parenting-advice literature; career pressures that impinge on parent involvement in children’s lives; abysmally weak American child-care services to assist employed parents in their child-rearing roles; cultural violence and excessive materialism permeating children’s worlds; schools with less than optimal conditions for children’s learning; and impediments to granting children with deficits and disabilities social experiences that maximize their development. Contemporary parents do not just find child rearing more difficult; they feel more uncertainty than their predecessors about whether and how to intervene in their children’s activities and behavior. In the pages that follow, I draw on major themes of this book—the power of adult warmth, appropriate expectations, narrative conversation, make-believe play, and teaching in the “zone”—to show how Vygotsky’s sociocultural approach can serve as a guide for resolving a great many child-rearing concerns. This chapter answers twenty questions drawn from a survey of over four hundred parents of 2- to 8-year-olds living in a Midwestern city with a population of one hundred thousand. In that survey, I asked parents to list any questions about young children’s development and learning that interested or worried them. The questions I answer here address issues that appeared most often in parents’ responses. Each represents a concern that surfaced in three or more parental replies. I intend these answers to parents’ questions to reflect a way of thinking about child rearing, not a set of recipes for dealing with specific events. When parents are familiar with principles that are grounded in contemporary theory and research on children’s development, they can better deal with the quandaries generated by the changing home, school, and community contexts in which today’s children grow up. Although adverse cultural trends have complicated and threatened good child rearing, parents—as agents of change, buffers against stressful life circumstances, and gatekeepers of learning opportunities—can do much to protect, restore, and reshape children’s experiences.
Konferenzberichte zum Thema "Parent satisfaction with child care services"
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Marković, Velisav. „USLUGA HRANITELjSTVA I PRAVA HRANITELjA“. In XV Majsko savetovanje: Sloboda pružanja usluga i pravna sigurnost. University of Kragujevac, Faculty of Law, 2019. http://dx.doi.org/10.46793/xvmajsko.639m.
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Foster care is a form of providing social care to a child or an adult provided by a foster family or foster parent living under the conditions prescribed by law and is a form of protecting a child without parental care, as well as a child under parental care in cases where there is a need to the child to live in another family. In Serbia, the foster parent has the right to receive compensations for foster care, social security contributions, certain rights arising from the employment related to foster care and the right to subsidies for utility services. In this article, the author presents the rights in relation to foster care in Serbia, as well as comparative law solutions.
Berichte der Organisationen zum Thema "Parent satisfaction with child care services"
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Dale, Naomi, Aneesa Khan und Sophie Dale. Early intervention for vision and neurodevelopment in infants and very young children with visual impairment: a systematicreview. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, August 2022. http://dx.doi.org/10.37766/inplasy2022.8.0080.
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Review question / Objective: Research question - What is the effectiveness of Early Childhood Intervention (ECI) in the first 3 years of life? Population (P) Infants and very young children with diagnosed visual impairment. Intervention (I) ECI programmes that includes vision and developmental stimulation, play, learning and responsive parenting Comparison (C) Standard care or control Outcomes (O) Primary: Vision function or and/or neurodevelopment and/or parent-child interaction outcomes Secondary: Parental context factors eg parental wellbeing and mental health, parental satisfaction with service provision. Condition being studied: Childhood congenital or very early visual impairment arising from congenital disorders of the peripheral or anterior visual system or cerebral-based vision disorders. This includes all vision disorders of the globe, retina and anterior optic nerve and all vision disorders that are considered cerebral based along visual pathways that are retro-chiasmatic and include central brain regions and networks involved in vision processing.
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Reddy, P. H. A qualitative study of quality of care in rural Karnataka. Population Council, 1995. http://dx.doi.org/10.31899/rh1995.1018.
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The Third Five-Year Plan (1961–66) aimed at reducing the crude birth rate in India to 25 per 1,000 population by 1973, however this goal has not been achieved. Several other demographic goals were set later, to be achieved by specified years, but they were deferred or revised. One major reason for the failure to achieve these goals was thought to be the lack of adequate infrastructural facilities for the family welfare program, thus it was decided to improve the institution–population ratio. The primary objective of this study is to assess the quality of interaction between clients and providers, and the quality of family welfare services. More specifically, the study examines how family welfare program personnel interact with clients in a given setting, the quality of interaction, how frequently such interaction takes place, the provider's view of, and satisfaction with, the information and quality of family welfare services provided, and the client's view of, and satisfaction with, the information and quality of family welfare services received. The focus of the investigation is on the family welfare program—the maternal and child health and family planning programs.
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District level baseline survey of family planning program in Uttar Pradesh: Sitapur. Population Council, 1995. http://dx.doi.org/10.31899/rh1995.1015.
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The Government of India and the United States Agency for International Development began the Innovations in Family Planning Services Projects (IFPS) in Uttar Pradesh under the management of the State Innovations in Family Planning Services Agency (SIFPSA). IFPS’s objectives are to increase access to family planning (FP) services, improve the quality of health care services, and promote contraceptive use. While achieving these goals, the IFPS project will support service innovations in the public and nongovernmental sectors, and contraceptive social marketing mechanisms. Baseline information being sought includes desired family size and sex preference among mothers, utilization of health services and immunization of mothers and children, maternal and child health care and delivery practices, contraceptive information and services and satisfaction with health providers, contraceptive use and unmet need, and media exposure and the role of the media in promoting small-family norm. The Operations Research Group, at the request of SIFPSA, has carried out the present baseline survey in the district of Sitapur. The baseline information will be used as the reference for the measurement of improvements in contraceptive use.
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District level baseline survey of family planning program in Uttar Pradesh: Shahjahanpur. Population Council, 1995. http://dx.doi.org/10.31899/rh1995.1014.
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The Government of India and the United States Agency for International Development began the Innovations in Family Planning Services Projects (IFPS) in Uttar Pradesh under the management of the State Innovations in Family Planning Services Agency (SIFPSA). IFPS’s objectives are to increase access to family planning (FP) services, improve the quality of health care services, and promote contraceptive use. While achieving these goals, the IFPS project will support service innovations in the public and nongovernmental sectors, and contraceptive social marketing mechanisms. Baseline information being sought includes desired family size and sex preference among mothers, utilization of health services and immunization of mothers and children, maternal and child health care and delivery practices, contraceptive information and services and satisfaction with health providers, contraceptive use and unmet need, and media exposure and the role of the media in promoting small-family norm. The Operations Research Group, at the request of SIFPSA, has carried out the present baseline survey in the district of Shahjahanpur. The information will be used as the reference for the measurement of improvements in contraceptive use.