Internet-based Physical Activity Promotion and Exercise Prescription for People With Multiple Sclerosis (ms bewegt)

April 27, 2021 updated by: Prof. Dr. Klaus Pfeifer, University of Erlangen-Nürnberg
The aim of the study is to evaluate the effects of a 12-week internet-based exercise and physical activity promotion intervention on physical activity. Furthermore, effects on symptoms of Multiple Sclerosis, Physical Activity-related Health Competence (PAHCO), self-concordance and basic needs satisfaction as well as usability and acceptability of the intervention will be investigated.

Study Overview

Study Type

Interventional

Enrollment (Actual)

62

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Bad Wildbad, Germany, 75323
        • Neurological Rehabilitation Center Quellenhof
      • Erlangen, Germany, 91058
        • Friedrich-Alexander University Erlangen-Nürnberg
      • Konstanz, Germany, 78464
        • Kliniken Schmieder Konstanz
      • Pforzheim, Germany, 75172
        • Facharztpraxis für Neurologie und Psychiatrie Dr. med Wolfgang Mattes und Andreas Stockert
      • Schwendi, Germany, 88477
        • Fachklinik für Neurologie Dietenbronn GmbH
      • Singen, Germany, 78224
        • E/M/S/A - Zentrum für Neurologie/Psychiatrie/Neuroradiologie
      • Stuttgart, Germany, 70174
        • Klinikum Stuttgart Katharinenhospital
      • Stuttgart, Germany, 70178
        • Neurologisch-Psychiatrische Praxis Dr. Weber
      • Würzburg, Germany, 97070
        • Klinikum Würzburg Mitte gGmbH

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • diagnosed Multiple Sclerosis (McDonald criteria)
  • Expanded Disability Status Scale between 0 - 6.5
  • neurologically stable (no exacerbation within 30 days prior to enrollment)
  • internet access (WiFi)
  • basic knowledge on handling personal computer and the internet
  • owning a smartphone with the operating system Android or IOS and with access to Google Play Store or Apple App score
  • basic computer and internet skills (e. g. using web browser and webcams)
  • ability to operate a smartphone (especially to install mobile applications)
  • ability to read, write and comprehend as well as communicate electronically

Exclusion Criteria:

  • regularly physically active (more than 30 minutes twice a week with at least moderate intensity; includes aerobic training, resistance training and other sports e.g. Tennis; excludes physiotherapy, physical activity during work or household, grocery shopping, gardening, walking the dog etc.)
  • clinically relevant cardiovascular diseases
  • cortisone therapy in the last 30 days
  • cognitive impairment that hampers study implementation
  • severe impairment of hand function (ataxia or paresis impeding the use of a smartphone app or smartwatch)
  • severe internal, orthopaedic and metabolic diseases that restrict mobility

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control
Experimental: Intervention
Participants receive a physical activity promotion intervention as well as an individualized exercise plan.
Physical activity promotion activities consist of two phone or video calls with a therapists, two group video calls with a therapist, a complementary e-learning course and a fitness tracker that was provided.
Participants will agree with their therapist on an exercise plan (endurance and resistance training) that will be made available through the studies mobile app. Frequency and duration of endurance and strength training shall be prescribed in accordance with exercise guidelines for persons with MS. However, they can be adjusted according to participants prior physical activity level and their time for exercise during the week.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in objectively measures physical activity
Time Frame: Baseline, after 3 months, after 6 months
The physical activity level of participants is measured over a 7 day period with the accelerometer Actigraph GT3X+. The Actigraph GT3X+ measures acceleration on three axes. Steps per day, physical activity per day (activity counts) and time in moderate and vigorous physical activity per day will be calculated.
Baseline, after 3 months, after 6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in subjectively measured physical activity: BSA-Questionnaire
Time Frame: Baseline, after 3 months, after 6 months
The questionnaire asks for physical activities during a typical week. It differentiates between leisure-time/transportation activities (physical activity score) and sport-/exercise-related activities (sports score). Participants are required to report frequency and duration of activities executed during the last two weeks. Minutes of leisure-time physical activity per week and sport-/exercise related activity per week are calculated to get the physical activity and the sports score. Both scores can combined in order to receive the overall volume of physical activity completed during leisure-time and transportation as well as sport-/exercise-related activities.
Baseline, after 3 months, after 6 months
Würzburger Fatigue Inventory for MS (WEIMuS)
Time Frame: Baseline, after 3 months, after 6 months
This questionnaire contains 17 items that form a physical and cognitive subscale. The total score ranges from zero to a maximum of 68 points (maximum fatigue). The cut-off value for the presence of fatigue is above 32.
Baseline, after 3 months, after 6 months
Allgemeine Depressionsskala (ADS-L)
Time Frame: Baseline, after 3 months, after 6 months
German version of the Center for Epidemiologic Studies Depression Scale, 20 item questionnaire. Each item is rated on a 4-point Likert scale. Answers are scored from 0 to 3. The scores for all items are added up to receive the total score. The total score ranges from 0 to 60 with higher scores representing higher levels of depression.
Baseline, after 3 months, after 6 months
Multiple Sclerosis Walking Scale-12
Time Frame: Baseline, after 3 months, after 6 months
12-item questionnaire measuring self reported walking ability. Each item is answered on a 5-point Likert scale. Answers are scored from 1 to 5. The scores for all items are added up to receive a total score. The total score ranges from 12 to 60 with higher scores representing higher levels of depression. As a last step the total score is transformed into the walk12-score ranging from 0 to 100 ((total score -12)/48 x 100 = walk12-score).
Baseline, after 3 months, after 6 months
Multiple Sclerosis Impact Scale (MSIS-29)
Time Frame: Baseline, after 3 months, after 6 months
An disease-specific questionnaire that measures quality of life and limitations due tu multiple sclerosis on two subscales (physical impact of MS, 20 items; psychological impact of MS, 9 items).Scores for both scales are generated by summing individual item scores and transforming the sum to a 0-100 scale. Higher scores represent worse health.
Baseline, after 3 months, after 6 months
Timed 25-Foot Walk Test (T25FW)
Time Frame: Baseline, after 3 months, after 6 months
The task is to walk a 25foot distance as fast as possible. This test measures the functionality of the lower extremity and the walking speed.
Baseline, after 3 months, after 6 months
Two-minute Walk Test (2MWT)
Time Frame: Baseline, after 3 months, after 6 months
The 2MWT measures walking endurance. It measures walking distance over 2 minutes. The subject is asked to walk as far as possible in 2 minutes.
Baseline, after 3 months, after 6 months
Selbstkonkordanz-Skala (SSK-Scale)
Time Frame: Baseline, after 3 months, after 6 months
The SSK-Scale measures self-rated physical activity-related and sports-related self-concordance. It contains 12 items which are assigned to 4 subscales: intrinsic, identified, introjected and extrinsic Motivation. An overall score can be calculated based on these four subscales (minimal score = -10, maximal Score = +10). To receive the overall score the scores of the subscales for introjected and extrinsic motivation will be subtracted from the sum of the identified and intrinsic motivation subscales. A high total score suggest a high level of physical activity-related and sports-related self-concordance.
Baseline, after 3 months, after 6 months
Physical activity-related health competence questionnaire
Time Frame: Baseline, after 3 months, after 6 months
44-item questionnaire that measures physical activity-related health competence. The physical activity related health competence consists of three subcompetencies: movement competence (20 items; min = 0, max = 17.6), control competence (10 items; min = 0, max = 10.8), PA-related self-regulation competence (14 items; min = 0, max = 14.8).
Baseline, after 3 months, after 6 months
German psychological need satisfaction in exercise scale
Time Frame: Baseline, after 3 months, after 6 months
This is a questionnaire to estimate the satisfaction of the three basic psychological needs based on self-determination theory during sports- and exercise related activities. It consists of 11 items which are assigned to 3 scales (one for each psychological need). Higher values on the scales indicate a higher needs satisfaction.
Baseline, after 3 months, after 6 months
Usability and usefulness of the mobile application (meCue 2.0 questionnaire)
Time Frame: after 3 months, after 6 months
The module usability and usefulness of the meCue 2.0 questionnaire was used. The module contains 3 items on usability and 3 items on usefulness that are answered on a 7-point Likert scale (scored from 1 to 7). In order two receive a score for usability and a score for usefulness, the mean is calculated for the items of each area.
after 3 months, after 6 months
Usability and usefulness of the intervention
Time Frame: after 3 months, after 6 months
Questionnaire including the Net Promoter Score and 45 self-developed items. Self-developed items covered willingness to pay, goal attainment, effects on physical function and wellbeing, adequacy of exercise prescription, evaluation of communication within the program, learning modules, App functions and activity trackers.
after 3 months, after 6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 1, 2019

Primary Completion (Actual)

July 30, 2020

Study Completion (Actual)

July 30, 2020

Study Registration Dates

First Submitted

April 21, 2020

First Submitted That Met QC Criteria

April 24, 2020

First Posted (Actual)

April 29, 2020

Study Record Updates

Last Update Posted (Actual)

April 28, 2021

Last Update Submitted That Met QC Criteria

April 27, 2021

Last Verified

April 1, 2021

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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