This paper is in the following e-collection/theme issue:

RCTs - Protocols/Proposals (eHealth) (668) Anxiety and Stress Disorders (1330) Depression and Mood Disorders; Suicide Prevention (1691) Supporting Home Care and Family Caregivers (262) Supporting Informal Care and Caregivers (381) Neurology and Neurosciences (286)

Published on in Vol 10, No 8 (2021): August

Preprints (earlier versions) of this paper are available at https://preprints.jmir.org/preprint/30617, first published .
Psychoeducational Interventions for Caregivers of Persons With Multiple Sclerosis: Protocol for a Randomized Trial

Psychoeducational Interventions for Caregivers of Persons With Multiple Sclerosis: Protocol for a Randomized Trial

Psychoeducational Interventions for Caregivers of Persons With Multiple Sclerosis: Protocol for a Randomized Trial

Authors of this article:

Sara L Douglas1 Author Orcid Image ;   Matthew Plow1 Author Orcid Image ;   Tanya Packer2, 3 Author Orcid Image ;   Amy R Lipson1 Author Orcid Image ;   Michelle J Lehman2 Author Orcid Image
Article Authors Cited by (9) Tweetations (9) Metrics

Journals

  1. Gómez-López A, Benito-León J, Labiano-Fontcuberta A, Moreno-García S, Salgado-Cámara P. Impact of a specific consultation for patients with progressive forms of multiple sclerosis on the response to their unmet care needs: a cross-sectional study. Multiple Sclerosis and Related Disorders 2023;72:104609 View
  2. Douglas S, Plow M. Psychometric Properties and Clinical Utility of the Distress Thermometer in Caregivers of Persons With Multiple Sclerosis. International Journal of MS Care 2023;25(3):93 View
  3. Douglas S, Plow M, Packer T, Lipson A, Lehman M. Effect of 2-Arm Intervention on Emotional Outcomes in Informal Caregivers of Individuals With Multiple Sclerosis: A Randomized Pilot Study Trial. International Journal of MS Care 2023;25(6):252 View
  4. Mousaei F, Mirhosseini S, Mafi M, Günaydın N, Zendehtalab H. Effect of support based on family centered empowerment model on care burden in family caregivers of patients with multiple sclerosis. Frontiers in Public Health 2023;11 View
  5. Packer T, Austin N, Lehman M, Douglas S, Plow M. Factors influencing how informal caregivers of people with multiple sclerosis access and use a curated intervention website: Analysis from an RCT. DIGITAL HEALTH 2024;10 View
  6. Culicetto L, Lo Buono V, Donato S, La Tona A, Cusumano A, Corello G, Sessa E, Rifici C, D’Aleo G, Quartarone A, Marino S. Importance of Coping Strategies on Quality of Life in People with Multiple Sclerosis: A Systematic Review. Journal of Clinical Medicine 2024;13(18):5505 View
  7. Poprelka K, Fasilis T, Patrikelis P, Ntinopoulou E, Margariti S, Verentzioti A, Stefanatou M, Alexoudi A, Stavrinou L, Korfias S, Gatzonis S. Burden in caregivers of adults with epilepsy: A critical review. Epilepsy & Behavior 2025;164:110260 View
  8. Mirhosseini S, Imani Parsa F, Moghadam-Roshtkhar H, Basirinezhad M, Ameri M, Ebrahimi H. Support based on psychoeducation intervention to address quality of life and care burden among caregivers of patients with cancer: a randomized controlled trial. Frontiers in Psychology 2025;16 View
  9. Poprelka K, Fasilis T, Patrikelis P, Ntinopoulou E, Verentzioti A, Stefanatou M, Alexoudi A, Stavrinou L, Korfias S, Gatzonis S. Mapping the landscape of caregiver burden in Huntington's Disease: Current evidence and future directions. Journal of Huntington's Disease 2025;14(4):304 View