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Accepted for/Published in: Journal of Medical Internet Research

Date Submitted: Feb 4, 2025
Date Accepted: May 30, 2025

The final, peer-reviewed published version of this preprint can be found here:

Family Caregivers of Individuals With Neuromuscular Disease Participating in a Randomized Controlled Trial of a Digital Peer Support Program: Nested Qualitative Study

Mekhuri S, Dale C, Buchanan F, Hammash N, Ambreen M, Saha S, Rose L, Amin R

Family Caregivers of Individuals With Neuromuscular Disease Participating in a Randomized Controlled Trial of a Digital Peer Support Program: Nested Qualitative Study

J Med Internet Res 2025;27:e72141

DOI: 10.2196/72141

PMID: 40720845

PMCID: 12303555

A Nested Qualitative Study of Family Caregivers of Individuals with Neuromuscular Disease Participating in a Randomized Controlled Trial of a Virtual Peer-Support Program

  • Samantha Mekhuri; 
  • Craig Dale; 
  • Francine Buchanan; 
  • Nouma Hammash; 
  • Munazzah Ambreen; 
  • Sian Saha; 
  • Louise Rose; 
  • Reshma Amin

ABSTRACT

Background:

Family caregivers have primary responsibility for providing care in the home for people with neuromuscular diseases (NMD). This may negatively affect caregiver health. Peer support may enhance quality of life and reduces stress among family caregivers, but few trials have been conducted in NMD caregivers. Therefore, we conducted a randomized controlled trial (RCT) with a nested qualitative evaluation (this report) of a 12-week virtual peer support intervention for family caregivers of children and adults with NMD.

Objective:

To gain insights into the perspectives of participants and peer mentors regarding their experiences with the trial’s virtual peer support program.

Methods:

We conducted an exploratory qualitative study (August 2022 to March 2024), recruiting participants and mentors to participate in semi-structured interviews via video conferencing. Homophily theory and the Theoretical Framework of Acceptability informed our analyses.

Results:

We interviewed 21 participants and 10 mentors, identifying four themes: (1) Program Participation Motivators; (2) Program Expectations and Appreciation; (3) Program Appropriateness; and (4) The Peer Mentor-Mentee Dyad. We found participants were motivated to join the program due to existing caregiver burden and social isolation. Participants and mentors appreciated the program’s sense of community and flexible virtual format, with participants valuing the emotional and informational support. However, challenges in relating to each other’s situations due to participant and mentor heterogeneity in the extent of care recipient’s needs were perceived to limit benefit.

Conclusions:

Peer support was perceived as potentially beneficial in relieving caregiver burden and social isolation creating a sense of community that provides emotional and informational support. The virtual and flexible format was an important facilitator. An important barrier was participant-mentor heterogeneity resulting in reduced perception of homophily. These findings can inform development of other virtual peer support programs to alleviate caregiver burden and isolation and to provide emotional relief and informational guidance. Clinical Trial: The RCT was registered with clinicaltrials.gov: NCT05070624, https://clinicaltrials.gov/study/NCT05070624.


 Citation

Please cite as:

Mekhuri S, Dale C, Buchanan F, Hammash N, Ambreen M, Saha S, Rose L, Amin R

Family Caregivers of Individuals With Neuromuscular Disease Participating in a Randomized Controlled Trial of a Digital Peer Support Program: Nested Qualitative Study

J Med Internet Res 2025;27:e72141

DOI: 10.2196/72141

PMID: 40720845

PMCID: 12303555

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