Prioritizing Components of a Dyadic Physical Activity Intervention for People With Moderate to Severe Multiple Sclerosis and Their Care Partners: A Modified e-Delphi Study

Author:

Fakolade Afolasade1ORCID,McKenna Odessa2,Kamel Rachel23,Freedman Mark S.45,Finlayson Marcia1,Latimer-Cheung Amy E.6,Pilutti Lara A.27

Affiliation:

1. From the School of Rehabilitation Therapy (AF, MF), Queen’s University, Kingston, ON, Canada.

2. From the Interdisciplinary School of Health Sciences (OM, RK, LAP), University of Ottawa, Ottawa, ON, Canada.

3. From the Biomedical Sciences, Faculty of Science (RK), University of Ottawa, Ottawa, ON, Canada.

4. From the Faculty of Medicine (MSF), University of Ottawa, Ottawa, ON, Canada.

5. From the Ottawa Hospital Research Institute, Ottawa, ON, Canada (MSF).

6. From the School of Kinesiology and Health Studies (AEL-C), Queen’s University, Kingston, ON, Canada.

7. From the Brain and Mind Research Institute (LAP), University of Ottawa, Ottawa, ON, Canada.

Abstract

ABSTRACT BACKGROUND People with moderate to severe multiple sclerosis (MS) and their family care partners do not engage in sufficient physical activity (PA) for health benefits. Dyadic PA interventions need to be developed to benefit each individual and the dyad. The objective of this study was to engage expert stakeholders in prioritizing and refining key intervention content, delivery methods, and the practical/logistical aspects of a dyadic PA intervention for persons with MS and their care partners. METHODS Thirty-two stakeholders (14 clinicians, 11 people with MS, 5 MS care partners, and 2 representatives of organizations that provide support services for people with MS and/or MS care partners) completed 2 rounds of a modified e-Delphi survey. In round 1, participants rated items across 3 domains: key intervention content (n = 8), delivery methods (n = 9), and practical/logistical aspects (n = 4). Participants contributed additional ideas about these domains, which were incorporated into round 2. Items that did not reach consensus in round 1 were forwarded to round 2 for rerating. Data were analyzed using descriptive statistics and content analysis. RESULTS A 24-item list of recommendations was generated, including ensuring that presentation of the intervention content encouraged lifestyle activities in addition to exercise, using videoconferencing rather than teleconferencing as a delivery platform, and stressing the importance of flexibility during the support calls. CONCLUSIONS Feedback will be used to improve the quality of the intervention. The next step in this line of research involves evaluating the refined intervention in a pilot feasibility trial.

Publisher

Consortium of Multiple Sclerosis Centers

Subject

Advanced and Specialized Nursing,Neurology (clinical)

Reference36 articles.

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2. Caregiver burden in multiple sclerosis: recent trends and future directions;Maguire;Curr Neurol Neurosci Rep.,2020

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