N/A
N=5
Theory Based Intervention Program to Support Physical Activity for Individuals With Multiple Sclerosis: a Case Series
Multiple Sclerosis
Bottom Line
View on ClinicalTrials.gov: NCT02335450 ↗Enrolled (actual)
5
Serious AEs
0.0%
Results posted
Aug 2020
Primary outcome: Primary: Total Steps Taken Over Course of the Study — 296,147 steps over 4 weeks
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Motivational Interviewing (Behavioral); Wristband physical activity monitor (Device)
- Age
- Adult, Older Adult · 19+ yrs
- Sex
- All
- Sponsor
- Oakland University
- Primary completion
- Nov 2015
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Total Steps Taken Over Course of the Study |
296,147 | — |
| SECONDARY Exercise Self-Efficacy Questionnaire |
73.65; 91.75 | — |
| SECONDARY Multiple Sclerosis Self-Efficacy Scale |
48.25; 47.25 | — |
| SECONDARY Multiple Sclerosis Impact Scale |
78.25; 65 | — |
Summary
This study evaluates the effectiveness of personalized physical activity coaching combined with the use of a physical activity monitor to support increased levels of daily physical activity in individuals with multiple sclerosis. All five participants will receive the intervention over the four week intervention phase.
Eligibility Criteria
Inclusion Criteria
- must have a physician diagnosis of multiple sclerosis and deemed suitable for engaging in a physical activity program by their physician
- must be ambulatory with or without an assistive device
- must be able to speak and read English
- must have a home computer or device capable of tracking and recording the daily Fitbit physical activity reports
Exclusion Criteria
- participants will be excluded if any contraindications to engaging in independent exercise are identified during the intake examination by the physical therapist: cardiovascular issues or safety issues with walking.
Data sourced from ClinicalTrials.gov (NCT02335450). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.