Physical Activity in Persons Newly Diagnosed With Multiple Sclerosis
Study Details
Study Description
Brief Summary
This single group pre-post pilot intervention will examine the feasibility and initial effect of a 12-week behavioral intervention, based on the Behavior Change Wheel and Capability-Opportunity-Motivation-Behavior (COM-B) model and remotely delivered through electronic newsletters and online one-on-one video conferencing, for promoting physical activity and secondarily reducing fatigue and quality of life in persons newly diagnosed with MS (diagnosed with MS within the past 2 years). The investigators hypothesize the proposed 12-week intervention will be feasible based on process, resource, management, and scientific outcomes. The investigators further hypothesize that individuals who receive the 12-week intervention will demonstrate an increase in physical activity behavior, particularly daily step counts, and reduce fatigue.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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N/A |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Capability-Opportunity-Motivation-Behavior (COM-B) based physical activity behavioral intervention This is a 1-arm study with an intervention condition based on the COM-B model |
Behavioral: Physical activity behavioral intervention in persons newly diagnosed with MS
The newsletters will provide the knowledge, skills, resources, and strategies for promoting physical activity in persons newly diagnosed with MS. These newsletters will be released seven times during the program. The first three newsletters will be released weekly, and the last four will be released every other week.
The one-on-one video coaching chats with participants will be conducted via Zoom, which consist of discussion and elaboration of newsletters content, supportive accountability, feedback and encouragement on behavior change. The chats further provide social persuasion for promoting behavior change. The chats are semi-scripted and individualized interventions (~15 - 30 minutes/chat). The chats will occur seven times during the week when a newsletter is delivered.
The intervention includes a pedometer (NL-800 pedometer), a logbook, and a calendar for tracking daily step counts, planning of physical activity, setting goals, and monitoring progress over the program.
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Outcome Measures
Primary Outcome Measures
- Feasibility metric: Process [12 weeks]
Process assesses participant recruitment, retention, and adherence i. Recruitment and refusal rates ii. Retention, attrition, and adherence rates to study procedures
- Feasibility metric: Resource [12 weeks]
We will assess the resources required for the study.
- Feasibility metric: Management [12 weeks]
Management assesses data management.
- Feasibility metric: Overall safety [12 weeks]
Overall safety will be assessed through the number of adverse events.
- Change of Physical Activity levels through Accelerometry from baseline and 12 weeks [12 weeks]
Physical activity will be assessed using an ActiGraph accelerometer. Participants will wear an accelerometer on a belt around their waist during the waking hours of a 7 day period. Participants will complete this at baseline and 12 weeks
- Change of Physical Activity levels through the Godin Leisure-Time Exercise Questionnaire from baseline and 12 weeks [12 weeks]
Physical activity will be assessed using the Godin Leisure-Time Exercise Questionnaire. Participants will complete this questionnaire at baseline and 12 weeks.
- Change of Physical Activity levels through the Abbreviated International Physical Activity Questionnaire from baseline and 12 weeks [12 weeks]
Physical activity will be assessed using the Abbreviated International Physical Activity Questionnaire. Participants will complete this questionnaire at baseline and 12 weeks.
Secondary Outcome Measures
- Change of self-report measures of Fatigue through the Fatigue Severity Scale from baseline and 12 weeks [12 weeks]
Self report measures of fatigue will be assessed through the Fatigue Severity Scale. Participants will complete this questionnaire at baseline and 12 weeks
- Changes of self-report measures of quality of life through the Multiple Sclerosis Impact Scale-29 at baseline and 12 weeks [12 weeks]
Self report measures of quality of life will be assessed through the Multiple Sclerosis Impact Scale-29.Participants will complete this questionnaire at baseline and 12 weeks
- Formative evaluation [12 weeks]
Participants' satisfaction in the study will be assessed through a self-developed survey which will be completed at 12 week.
Eligibility Criteria
Criteria
Inclusion Criteria:
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≥ 18 years old
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Diagnosed with multiple sclerosis for 2 or fewer years
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Fully ambulatory
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No relapse within the last 30 days
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Non-active (Godin Leisure-Time Exercise Questionnaire - Health Contribution Score <
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Able to read 14-point font size
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Internet & video conferencing access
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Undergoing disease-modifying therapy
Exclusion Criteria:
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Pregnancy
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Moderate or high risk for undertaking physical activity (≥ 2 affirmatives on the Physical Activity Readiness Questionnaire)
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University of Alabama at Birmingham | Birmingham | Alabama | United States | 35205 |
Sponsors and Collaborators
- University of Alabama at Birmingham
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- IRB-300009893