Citations (24)
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Kenneth I. Pakenham. (2008) The nature of sense making in caregiving for persons with multiple sclerosis. Disability and Rehabilitation 30:17, pages 1263-1273.
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KarenI. Fredriksen-Goldsen & NancyR. Hooyman. (2007) Caregiving Research, Services, and Policies in Historically Marginalized Communities. Journal of Gay & Lesbian Social Services 18:3-4, pages 129-145.
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KI Pakenham, VA Goodwin & JC MacMillan. (2004) Adaptation to being at-risk for Huntington's Disease and the availability of genetic testing: application of a stress and coping model. Psychology, Health & Medicine 9:3, pages 380-397.
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J. Mccausland & K.I. Pakenham. (2003) Investigation of the benefits of HIV/AIDS caregiving and relations among caregiving adjustment, benefit finding, and stress and coping variables. AIDS Care 15:6, pages 853-869.
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Articles from other publishers (20)
Marcia Finlayson & Kenneth Pakenham. (2023) Opportunities in Multiple Sclerosis Care Partner Research: An Interview. International Journal of MS Care 25:6, pages 278-280.
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Aimee Dietz, E. Susan Duncan, Lauren Bislick, Sarah Stegman, Jenna Collins, Chitrali Mamlekar, Rachel Gleason & Michael J. McCarthy. (2020) Yoga as Therapy for People With Aphasia. Perspectives of the ASHA Special Interest Groups 5:4, pages 853-860.
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Kennedy Nkhoma, Christine Norton, Caroline Sabin, Alan Winston, Jessica Merlin & Richard Harding. (2018) Self-management Interventions for Pain and Physical Symptoms Among People Living With HIV: A Systematic Review of the Evidence. JAIDS Journal of Acquired Immune Deficiency Syndromes 79:2, pages 206-225.
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Natalie Flath, Karin Tobin, Aleks Mihailovic, Paige Hammond & Carl Latkin. (2018) Evaluating a Dyadic Intervention on Risk Reduction Among People Who Inject Drugs. Substance Abuse: Research and Treatment 12, pages 117822181879975.
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Lorraine S. Evangelista, Anna Strömberg & J. Nicholas Dionne-Odom. (2016) An integrated review of interventions to improve psychological outcomes in caregivers of patients with heart failure. Current Opinion in Supportive & Palliative Care 10:1, pages 24-31.
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Ranak B. Trivedi, Jackie G. Szarka, Kristine Beaver, Koriann Brousseau, Elaine Nevins, William S. YancyJr.Jr., Alecia Slade & Corrine I. Voils. (2013) Recruitment and retention rates in behavioral trials involving patients and a support person: A systematic review. Contemporary Clinical Trials 36:1, pages 307-318.
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Rosemary W. Eustace. (2012)
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Christina Mackay & Kenneth I. Pakenham. (2011) A Stress and Coping Model of Adjustment to Caring for an Adult with Mental Illness. Community Mental Health Journal 48:4, pages 450-462.
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Lorena Chaparro. (2011) How a "Special Caring Bond" is Formed Between the Chronically ill Patient and the Family Caregiver. Aquichan 11:1, pages 7-22.
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Debra Haire-Joshu, Michael B. Elliott, Nicole M. Caito, Kimberly Hessler, M.S. Nanney, Nancy Hale, Tegan K. Boehmer, Matthew Kreuter & Ross C. Brownson. (2008) High 5 for Kids: The impact of a home visiting program on fruit and vegetable intake of parents and their preschool children. Preventive Medicine 47:1, pages 77-82.
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Urmi Nanda Biswas. (2016) Promoting Health and Well-being in Lives of People Living with HIV and AIDS. Psychology and Developing Societies 19:2, pages 215-247.
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Michael D. Stein, Debra S. Herman, Duane Bishop, Bradley J. Anderson, Elizabeth Trisvan, Rosalie Lopez, Timothy Flanigan & Ivan Miller. (2006) A Telephone-Based Intervention for Depression in HIV Patients: Negative Results from a Randomized Clinical Trial. AIDS and Behavior 11:1, pages 15-23.
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Carmen Fuentelsaz-Gallego, Inmaculada Úbeda-Bonet, Montserrat Roca-Roger, Teresa Faura-Vendrell, Anna M. Salas-Pérez, Dolors Buisac-González, Carmen López-Mateu & Montserrat Lacarcel-Comas. (2006) Características y calidad de vida de los cuidadores informales de enfermos de sida. Enfermería Clínica 16:3, pages 137-143.
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Debra S. Herman, Duane Bishop, Jennifer L. Anthony, William Chase, Elizabeth Trisvan, Rosalie Lopez & Michael D. Stein. (2006) Feasibility of a Telephone Intervention for HIV Patients and Their Informal Caregivers. Journal of Clinical Psychology in Medical Settings 13:1, pages 78-88.
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Paul A. Pirraglia, Duane Bishop, Debra S. Herman, Elizabeth Trisvan, Rosalie A. Lopez, Christopher S. Torgersen, Ann Marie Hof, Bradley J. Anderson, Ivan Miller & Michael D. Stein. (2005) Caregiver burden and depression among informal caregivers of HIV-infected individuals. Journal of General Internal Medicine 20:6, pages 510-514.
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Kenneth I. Pakenham. (2005) Relations Between Coping and Positive and Negative Outcomes in Carers of Persons with Multiple Sclerosis (MS). Journal of Clinical Psychology in Medical Settings 12:1, pages 25-38.
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G Green & R Smith. (2004) The psychosocial and health care needs of HIV-positive people in the United Kingdom: a review. HIV Medicine 5:s1, pages 4-46.
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