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Physical Activity in Persons Newly Diagnosed With Multiple Sclerosis

Physical Activity Intervention for Persons Newly Diagnosed With Multiple Sclerosis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05641532
Enrollment
16
Registered
2022-12-07
Start date
2023-01-17
Completion date
2023-08-08
Last updated
2023-08-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Sclerosis (MS)

Keywords

Physical activity, Newly diagnosed with MS, Behavior change, Multiple sclerosis

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.

Interventions

BEHAVIORALPhysical activity behavioral intervention in persons newly diagnosed with MS

1. 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. 2. 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. 3. 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.

Sponsors

University of Alabama at Birmingham
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

All participants will undergo one intervention condition remotely delivered using electronic newsletters and one-on-one video coaching. Outcome measures will be assessed at two time points: baseline and post-intervention.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* ≥ 18 years old * Diagnosed with multiple sclerosis for 2 or fewer years * Fully ambulatory * No relapse within the last 30 days * Non-active (Godin Leisure-Time Exercise Questionnaire - Health Contribution Score \< 14) * Able to read 14-point font size * Internet & video conferencing access * Undergoing disease-modifying therapy

Exclusion criteria

* Pregnancy * Moderate or high risk for undertaking physical activity (≥ 2 affirmatives on the Physical Activity Readiness Questionnaire)

Design outcomes

Primary

MeasureTime frameDescription
Change of Physical Activity levels through the Abbreviated International Physical Activity Questionnaire from baseline and 12 weeks12 weeksPhysical activity will be assessed using the Abbreviated International Physical Activity Questionnaire. Participants will complete this questionnaire at baseline and 12 weeks.
Feasibility metric: Overall safety12 weeksOverall safety will be assessed through the number of adverse events.
Change of Physical Activity levels through Accelerometry from baseline and 12 weeks12 weeksPhysical 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 weeks12 weeksPhysical activity will be assessed using the Godin Leisure-Time Exercise Questionnaire. Participants will complete this questionnaire at baseline and 12 weeks.
Feasibility metric: Process12 weeksProcess assesses participant recruitment, retention, and adherence i. Recruitment and refusal rates ii. Retention, attrition, and adherence rates to study procedures
Feasibility metric: Resource12 weeksWe will assess the resources required for the study.
Feasibility metric: Management12 weeksManagement assesses data management.

Secondary

MeasureTime frameDescription
Changes of self-report measures of quality of life through the Multiple Sclerosis Impact Scale-29 at baseline and 12 weeks12 weeksSelf 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 evaluation12 weeksParticipants' satisfaction in the study will be assessed through a self-developed survey which will be completed at 12 week.
Change of self-report measures of Fatigue through the Fatigue Severity Scale from baseline and 12 weeks12 weeksSelf report measures of fatigue will be assessed through the Fatigue Severity Scale. Participants will complete this questionnaire at baseline and 12 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026