Artykuły w czasopismach na temat „Caregivers”
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Savla, Jyoti, Karen Roberto i Rosemary Blieszner. "CARE NETWORKS OF RURAL APPALACHIAN FAMILY CAREGIVERS AND PERSONS LIVING WITH DEMENTIA". Innovation in Aging 6, Supplement_1 (1.11.2022): 194. http://dx.doi.org/10.1093/geroni/igac059.776.
Pełny tekst źródłaMessias, Lisiane Alves dos Santos, Fátima Adriana D'Almeida Gazetta, Pedro Marco Karan Barbosa i Zamir Calamita. "Conhecimento prático e sobrecarga na vida de cuidadores de idosos com demência". Scientia Medica 28, nr 3 (31.08.2018): 30569. http://dx.doi.org/10.15448/1980-6108.2018.3.30569.
Pełny tekst źródłaBuchanan, Robert J., i Chunfeng Huang. "The Need for Mental Health Care Among Informal Caregivers Assisting People with Multiple Sclerosis". International Journal of MS Care 15, nr 2 (1.06.2013): 56–64. http://dx.doi.org/10.7224/1537-2073.2012-030.
Pełny tekst źródłaFrias, Cindy E., Esther Cabrera i Adelaida Zabalegui. "Informal Caregivers’ Roles in Dementia: The Impact on Their Quality of Life". Life 10, nr 11 (23.10.2020): 251. http://dx.doi.org/10.3390/life10110251.
Pełny tekst źródłaAngelika, Putu Veby, The Maria Meiwati Widagdo, Widya Christine Manus i Silvester Haripurnomo. "CORRELATION STUDY BETWEEN BURDENS AND THE QUALITY OF LIFE IN CAREGIVERS OF DEPENDENT ELDERLY IN PRAWIRODIRJAN VILLAGE". Journal of Widya Medika Junior 4, nr 2 (kwiecień 2022): 114–24. http://dx.doi.org/10.33508/jwmj.v4i2.3779.
Pełny tekst źródłaYousaf, Aiza, Hira Iqbal, Rabeea Zubair, Muhammad Kashif, Danish Hassan i Rizwan Ahmed. "Factors associated with caregiver burden among caregivers of cerebral palsy children." Professional Medical Journal 27, nr 08 (10.08.2020): 1555–59. http://dx.doi.org/10.29309/tpmj/2020.27.08.3781.
Pełny tekst źródłaChou, Yueh-Ching, Li-yeh Fu, Li-Chan Lin i Yue-Chune Lee. "Predictors of subjective and objective caregiving burden in older female caregivers of adults with intellectual disabilities". International Psychogeriatrics 23, nr 4 (12.08.2010): 562–72. http://dx.doi.org/10.1017/s1041610210001225.
Pełny tekst źródłaKrishnan, Shilpa, Haobin Tony Chen, Sarah Caston i Seunghwa Rho. "Physical and Psychological Burden among Caregivers of Latinx Older Adults with Stroke and Multimorbidity". Ethnicity & Disease 33, nr 4 (1.12.2023): 156–62. http://dx.doi.org/10.18865/ed.33.4.156.
Pełny tekst źródłaBraun, Michal, Mario Mikulincer, Anne Rydall, Andrew Walsh i Gary Rodin. "Hidden Morbidity in Cancer: Spouse Caregivers". Journal of Clinical Oncology 25, nr 30 (20.10.2007): 4829–34. http://dx.doi.org/10.1200/jco.2006.10.0909.
Pełny tekst źródłaGrivel, Charlotte, Pierre Nizet, Manon Martin, Solange Pécout, Aurélie Lepeintre, Yann Touchefeu, Sonia Prot-Labarthe, Adrien Evin i Jean-François Huon. "The experience of being a caregiver of patients with digestive cancer, from patients and caregivers’ perception: A mixed study". PLOS ONE 18, nr 7 (21.07.2023): e0287335. http://dx.doi.org/10.1371/journal.pone.0287335.
Pełny tekst źródłaDavis, Abigail Oluwadunni, Oladapo Michael Olagbegi, Kayode Orekoya, Mathew Adekunle, Olufemi Oyeleye Oyewole, Modinat Adepoju i Oluyemisi Soetan. "Burden and quality of life of informal caregivers of children with cerebral palsy". Rev Rene 22 (3.05.2021): e61752. http://dx.doi.org/10.15253/2175-6783.20212261752.
Pełny tekst źródłaNovak, Mark, i Carol Guest. "Caregiver Response to Alzheimer's Disease". International Journal of Aging and Human Development 28, nr 1 (styczeń 1989): 67–79. http://dx.doi.org/10.2190/4w02-hlmk-hamj-utqp.
Pełny tekst źródłaParker Oliver, Debra, George Demiris, Karla Washington, Robin L. Kruse i Greg Petroski. "Hospice Family Caregiver Involvement in Care Plan Meetings: A Mixed-Methods Randomized Controlled Trial". American Journal of Hospice and Palliative Medicine® 34, nr 9 (27.07.2016): 849–59. http://dx.doi.org/10.1177/1049909116661816.
Pełny tekst źródłaChiari, Annalisa, Barbara Pistoresi, Chiara Galli, Manuela Tondelli, Giulia Vinceti, Maria Angela Molinari, Tindara Addabbo i Giovanna Zamboni. "Determinants of Caregiver Burden in Early-Onset Dementia". Dementia and Geriatric Cognitive Disorders Extra 11, nr 2 (13.08.2021): 189–97. http://dx.doi.org/10.1159/000516585.
Pełny tekst źródłaKim, Sun Kyung, Myonghwa Park, Yunhwan Lee, Seong Hye Choi, So Young Moon, Sang Won Seo, Kyung Won Park i in. "Influence of personality on depression, burden, and health-related quality of life in family caregivers of persons with dementia". International Psychogeriatrics 29, nr 2 (26.10.2016): 227–37. http://dx.doi.org/10.1017/s1041610216001770.
Pełny tekst źródłaSavitri, Wenny, i Suwarno. "Kualitas Hidup Family Caregiver Pasien Kanker dan Faktor-Faktor yang Mempengaruhinya". MEDIA ILMU KESEHATAN 11, nr 1 (2.01.2023): 46–55. http://dx.doi.org/10.30989/mik.v11i1.667.
Pełny tekst źródłaMeinertz, Naomi. "POWERFUL TOOLS FOR CAREGIVERS: THE ESTABLISHED BENEFITS OF A PERSON-CENTERED CARE INTERVENTION". Innovation in Aging 7, Supplement_1 (1.12.2023): 369–70. http://dx.doi.org/10.1093/geroni/igad104.1227.
Pełny tekst źródłaLeung, D. Y. P. "13 Caregiving Burden and Unmet Support Needs in Chinese Caregivers and Cancer Patients". Age and Ageing 50, Supplement_1 (marzec 2021): i1—i6. http://dx.doi.org/10.1093/ageing/afab028.13.
Pełny tekst źródłaWoerpel, Allison J., Willie Winston i Sonya S. Brady. "Stressful Life Circumstances, Resources for Support, and African American Children’s Psychological Symptoms". Journal of Black Psychology 43, nr 4 (26.04.2016): 327–44. http://dx.doi.org/10.1177/0095798416645717.
Pełny tekst źródłaJutkowitz, Eric, Daniel Scerpella, Katherine Prioli, Katherine Marx, Laura N. Gitlin, Laura Pizzi i Jonah Popp. "CHANGE IN DEMENTIA FAMILY CAREGIVERS’ WILLINGNESS TO PAY FOR A NONPHARMACOLOGIC INTERVENTION". Innovation in Aging 3, Supplement_1 (listopad 2019): S551. http://dx.doi.org/10.1093/geroni/igz038.2030.
Pełny tekst źródłade Rosa, Cristina, Ashleigh Holmes, Weijun Wang i Yu-Ping Chang. "POSITIVE CAREGIVING AND CAREGIVING RELATIONSHIP ASSOCIATION WITH MENTAL HEALTH AND PERCEIVED GENERAL HEALTH". Innovation in Aging 6, Supplement_1 (1.11.2022): 542. http://dx.doi.org/10.1093/geroni/igac059.2057.
Pełny tekst źródłaKristina, Hana, The Maria Meiwati Widagdo i Teguh Kristian Perdamaian. "STUDY CORRELATION BETWEEN BURDEN AND QUALITY OF LIFE OF DEPENDENT ELDERLY CAREGIVERS IN KLITREN, YOGYAKARTA". Journal of Widya Medika Junior 4, nr 1 (styczeń 2022): 1. http://dx.doi.org/10.33508/jwmj.v4i1.3321.
Pełny tekst źródłaCurrie, Janet M., Michele Mercer, Russ Michael i Daniel Pichardo. "New Caregiver Diagnoses of Severe Depression and Child Asthma Controller Medication Adherence". International Journal of Environmental Research and Public Health 20, nr 11 (29.05.2023): 5986. http://dx.doi.org/10.3390/ijerph20115986.
Pełny tekst źródłaReckrey, Jennifer, Deborah Watman i Emma Tsui. "Whose Decision Is It? Perspectives on Agency Involvement in Determining Paid Caregivers' Roles in Dementia Care". Innovation in Aging 5, Supplement_1 (1.12.2021): 217. http://dx.doi.org/10.1093/geroni/igab046.836.
Pełny tekst źródłaJoy, Jomon, Hussain Khan T. J., Pretty M. Abraham i Sreedas Gopalakrishnan. "Burden and resilience in caregivers of patients on maintenance haemodialysis". International Journal of Research in Medical Sciences 7, nr 11 (24.10.2019): 4033. http://dx.doi.org/10.18203/2320-6012.ijrms20194586.
Pełny tekst źródłaKim, Yoonjoo. "The Impact of Depression on Quality of Life in Caregivers of Cancer Patients: A Moderated Mediation Model of Spousal Relationship and Caring Burden". Current Oncology 29, nr 11 (27.10.2022): 8093–102. http://dx.doi.org/10.3390/curroncol29110639.
Pełny tekst źródłaLi, Lun, i Yeonjung Lee. "Caregiving Choice and Caregiver-Receiver Relation: Effects on Psychological Well-being of Family Caregivers in Canada". Canadian Journal on Aging / La Revue canadienne du vieillissement 39, nr 4 (10.02.2020): 634–46. http://dx.doi.org/10.1017/s0714980819000825.
Pełny tekst źródłaBeverly, Alexis, Christina Baucco, Seho Park, Matthew Schroeder, Shelley Johns, Katherine Judge i Nicole Fowler. "THE RELATIONSHIP BETWEEN SOCIOECONOMIC DISADVANTAGE AND DEMENTIA CAREGIVER BURDEN". Innovation in Aging 6, Supplement_1 (1.11.2022): 769. http://dx.doi.org/10.1093/geroni/igac059.2786.
Pełny tekst źródłaRamasamy, Thendral, Surendran Veeraiah i Kalpana Balakrishnan. "Psychosocial Issues Among Primary Caregivers of Patients with Advanced Head and Neck Cancer - A Mixed-method Study". Indian Journal of Palliative Care 27 (25.11.2021): 503–12. http://dx.doi.org/10.25259/ijpc_76_21.
Pełny tekst źródłaPutri, Yossie Susanti Eka, I. Gusti Ngurah Edi Putra, Annida Falahaini i Ice Yulia Wardani. "Factors Associated with Caregiver Burden in Caregivers of Older Patients with Dementia in Indonesia". International Journal of Environmental Research and Public Health 19, nr 19 (29.09.2022): 12437. http://dx.doi.org/10.3390/ijerph191912437.
Pełny tekst źródłaJiang, Hantao, i Xueqing Wang. "HEALTHY CAREGIVER SELECTION AMONG DEMENTIA CAREGIVERS: THE ROLE OF SOCIAL SUPPORT". Innovation in Aging 6, Supplement_1 (1.11.2022): 872–73. http://dx.doi.org/10.1093/geroni/igac059.3117.
Pełny tekst źródłaKulkarni, Shubham S., Chaitanya Patil, Yogesh S. Anap, Prasad K. Tanawade, Parag J. Watve i Aditya S. Pawar. "Quality of Life of Primary Caregivers Attending a Rural Cancer Centre in Western Maharashtra: A Cross-Sectional Study". Indian Journal of Medical and Paediatric Oncology 42, nr 03 (maj 2021): 268–72. http://dx.doi.org/10.1055/s-0041-1735664.
Pełny tekst źródłaHu, Mengyao, Dena Schulman-Green, Emma Zang i Bei Wu. "POSITIVE ASPECTS OF CAREGIVING IN DIFFERENT CAREGIVER GROUPS". Innovation in Aging 6, Supplement_1 (1.11.2022): 66–67. http://dx.doi.org/10.1093/geroni/igac059.264.
Pełny tekst źródłaRuisoto, Pablo, Marina Ramírez, Belén Paladines-Costa, Silvia Vaca i Vicente Javier Clemente-Suárez. "Predicting Caregiver Burden in Informal Caregivers for the Elderly in Ecuador". International Journal of Environmental Research and Public Health 17, nr 19 (8.10.2020): 7338. http://dx.doi.org/10.3390/ijerph17197338.
Pełny tekst źródłaGallanis, Tony. "THE EFFECT OF ACTIVITIES OF DAILY LIVING ON FAMILY CAREGIVER SOCIAL ISOLATION". Innovation in Aging 3, Supplement_1 (listopad 2019): S899. http://dx.doi.org/10.1093/geroni/igz038.3286.
Pełny tekst źródłaZuo, Yan, Bi-Ru Luo, Wen-Tao Peng, Xin-Ru Liu, Ya-Lin He i Jian-Jun Zhang. "Informal caregiver burden and influencing factors in gynaecological oncology patients hospitalized for chemotherapy: a cross-sectional study". Journal of International Medical Research 48, nr 11 (listopad 2020): 030006052097492. http://dx.doi.org/10.1177/0300060520974927.
Pełny tekst źródłaLee, Cecilia, Jessica Brian, Yona Lunsky, Kenneth Fung, Rachelle Ashcroft, Rebecca Lerner i Melanie Penner. "17 Caregiver Mental Health Needs in Caregiver-Mediated Early Intervention". Paediatrics & Child Health 28, Supplement_1 (1.09.2023): e7-e8. http://dx.doi.org/10.1093/pch/pxad055.017.
Pełny tekst źródłaYu, Hua, Li Wu, Shu Chen, Qing Wu, Yuan Yang i Helen Edwards. "Caregiving burden and gain among adult-child caregivers caring for parents with dementia in China: the partial mediating role of reciprocal filial piety". International Psychogeriatrics 28, nr 11 (3.06.2016): 1845–55. http://dx.doi.org/10.1017/s1041610216000685.
Pełny tekst źródłaOpara, Józef, i W. Brola. "Quality of Life and Burden in caregivers of Multiple Sclerosis patients". Physiotherapy and Health Activity 25, nr 1 (1.03.2018): 9–16. http://dx.doi.org/10.1515/pha-2017-0002.
Pełny tekst źródłaWilliams, Anna-Leila, i Ruth McCorkle. "Cancer family caregivers during the palliative, hospice, and bereavement phases: A review of the descriptive psychosocial literature". Palliative and Supportive Care 9, nr 3 (15.08.2011): 315–25. http://dx.doi.org/10.1017/s1478951511000265.
Pełny tekst źródłaAlberts, Nicole M., Heather D. Hadjistavropoulos, Nicole E. Pugh i Shannon L. Jones. "Dementia anxiety among older adult caregivers: an exploratory study of older adult caregivers in Canada". International Psychogeriatrics 23, nr 6 (22.03.2011): 880–86. http://dx.doi.org/10.1017/s1041610211000299.
Pełny tekst źródłaAndruccioli, Jessica, Maria Maffia Russo, Angela Bruschi, Luigi Pedrabissi, Donatella Sarti, Maria Cristina Monterubbianesi, Sabina Rossi, Sabina Rocconi i William Raffaeli. "Death Representation of Caregivers in Hospice". American Journal of Hospice and Palliative Medicine® 29, nr 7 (12.01.2012): 531–35. http://dx.doi.org/10.1177/1049909111432623.
Pełny tekst źródłaBjørge, Heidi, Kari Kvaal, Milada Cvancarova Småstuen i Ingun Ulstein. "Relationship Quality and Distress in Caregivers of Persons With Dementia: A Cross-Sectional Study". American Journal of Alzheimer's Disease & Other Dementiasr 32, nr 3 (27.02.2017): 157–65. http://dx.doi.org/10.1177/1533317517691121.
Pełny tekst źródłaLerdal, Anners, Caryl L. Gay, Elisabeth Saghaug, Kaare Gautvik, Ellen Karine Grov, Are Normann, Joran Slaaen, Kari Slåtten, Oddveig Utheim Tallang i Kathryn A. Lee. "Sleep in family caregivers of patients admitted to hospice: A pilot study". Palliative and Supportive Care 12, nr 6 (6.08.2013): 439–44. http://dx.doi.org/10.1017/s1478951513000357.
Pełny tekst źródłaJütten, Linda Helena, Ruth Elaine Mark, Ben Wilhelmus Jacobus Maria Janssen, Jan Rietsema, Rose-Marie Dröes i Margriet Maria Sitskoorn. "Testing the effectivity of the mixed virtual reality training Into D’mentia for informal caregivers of people with dementia: protocol for a longitudinal, quasi-experimental study". BMJ Open 7, nr 8 (sierpień 2017): e015702. http://dx.doi.org/10.1136/bmjopen-2016-015702.
Pełny tekst źródłaSelin, Jennifer, Mary Schmitt i Margaret Hill. "Caregivers' Perceptions of Their Child's Language Disorder: Alignment between Caregivers and Speech–Language Pathologists". Seminars in Speech and Language 39, nr 05 (19.09.2018): 427–42. http://dx.doi.org/10.1055/s-0038-1670671.
Pełny tekst źródłaSawyer, Jean, Colleen Matteson, Hua Ou i Takahisa Nagase. "The Effects of Parent-Focused Slow Relaxed Speech Intervention on Articulation Rate, Response Time Latency, and Fluency in Preschool Children Who Stutter". Journal of Speech, Language, and Hearing Research 60, nr 4 (14.04.2017): 794–809. http://dx.doi.org/10.1044/2016_jslhr-s-16-0002.
Pełny tekst źródłaMeriggi, Fausto, Federica Andreis, Veronica Premi, Nadia Liborio, Claudio Codignola, Maria Mazzocchi, Anna Rizzi i in. "Assessing cancer caregivers' needs for an early targeted psychosocial support project: The experience of the oncology department of the Poliambulanza Foundation". Palliative and Supportive Care 13, nr 4 (26.06.2014): 865–73. http://dx.doi.org/10.1017/s1478951514000753.
Pełny tekst źródłaPooyania, Sepideh, Michelle Lobchuk, Wanda Chernomas i Ruth Ann Marrie. "Examining the Relationship Between Family Caregivers' Emotional States and Ability to Empathize with Patients with Multiple Sclerosis". International Journal of MS Care 18, nr 3 (1.05.2016): 122–28. http://dx.doi.org/10.7224/1537-2073.2015-023.
Pełny tekst źródłaSussman, Joleen, Lauren Moo i Michele Karel. "Using Video Telehealth to Support Family Caregivers of People With Dementia". Innovation in Aging 4, Supplement_1 (1.12.2020): 660–61. http://dx.doi.org/10.1093/geroni/igaa057.2282.
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