Physical Activity Level of Norwegian Boys With Duchenne Muscular Dystrophy

Sponsor
Haukeland University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT03947112
Collaborator
Norwegian School of Sport Sciences (Other), Oslo University Hospital (Other)
28
1
10.3
2.7

Study Details

Study Description

Brief Summary

The aim of this population based study is to examine, quantify and describe physical activity level in Norwegian boys with DMD, and to compare the level of physical activity level between boys with DMD and age matched healthy boys. A co-project will validate ActiGraph accelerometry to measure physical activity in boys with DMD.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Physical activity registration

Detailed Description

International guidelines recommend regular physical activity for boys with DMD, and participation in physical activity plays a key role in the management. Paradoxically, patients with severe neuromuscular disease like DMD, have considerable limitations to participate in such activities. Limitation may be muscle weakness, pain, fatigue, reduced mobility and overall function, and also limited knowledge of physical activity benefits among health care personnel. Limited participation leads to a sedentary lifestyle, and gradual under-use of still functioning muscles may cause secondary deterioration in DMD.

The current physical activity level amongst Norwegian DMD's are unknown, and physical activity registration and self-reported questionnaire will be examined in this study.

Study Design

Study Type:
Observational
Actual Enrollment :
28 participants
Observational Model:
Other
Time Perspective:
Cross-Sectional
Official Title:
Physical Activity Level of Norwegian Boys With Duchenne Muscular Dystrophy - a Cross Sectional Study
Actual Study Start Date :
Aug 20, 2020
Actual Primary Completion Date :
Jun 30, 2021
Actual Study Completion Date :
Jun 30, 2021

Arms and Interventions

Arm Intervention/Treatment
Norwegian population with Duchenne Muscular Dystrophy (DMD)

Boys with DMD.

Behavioral: Physical activity registration
At start, participants and parents fills out a Self-report questionnaire and the UngKan-3 Questionnaire, before a seven day physical activity registration takes place by use og ActiGraph. A physical activity diary are filled out every evening while the physical activity registration takes places.
Other Names:
  • Self-report Questionnaire
  • Physical activity diary
  • UngKan-3 Questionnaire
  • Outcome Measures

    Primary Outcome Measures

    1. Physical activity registration [Seven days]

      An Actigraph will be provided and worn at pre set time frame (Seven days including weekend). Data extracted are counts per minutes, and are measurements of movement performed in both vertical and horizontal axis. The counts will be used to quantify the time the participant is inactive, low, moderate and / or in vigorous physical active.

    Secondary Outcome Measures

    1. Leisure time physical activity [Day 1]

      The UngKan-3 questionnaire is a self-reported/parent-reported instrument, developed to measure leisure time physical activity, diet, media habits and sleep routine. The questionnaire is former used in a national cross-sectional survey amongst Norwegian school students, developed by the Norwegian School of Sport Sciences and Norwegian Institute of Public Health.

    2. Self-Reported Questionnaire [Day 1]

      Self-administrated questionnaire developed to describe participants function, on-going treatment, movement aid, types of physical activities

    Other Outcome Measures

    1. Physical Activity diary [Day 1]

      During physical activity registration with use of ActiGraph monitor, the participants and parents are asked to fill out a diary, describing type of physical activity been performed, for how long the physical activity was performed, how tired the participants became, and how did the participant enjoy the activity being performed. In addition the participants is asked to give a summary of the week regarding to name the most enjoyable activity this week and the reason why, and to describe if there occurred something unusual that increased or decreased their physical activity level more than regular.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    6 Years to 18 Years
    Sexes Eligible for Study:
    Male
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Boys with conclusive diagnosis of Duchenne Muscular disease, attending Norwegian pediatric rehabilitation clinics.

    • Signed written consent

    • Able to answer questionnaires with help from parents, care giver(s) or health care professional with regular follow up of the participants.

    Exclusion Criteria:
    • Lack of consent.

    • Language difficulties

    • Cognitive dysfunction or mental retardation leading to difficulties in answering the questionnaires adequately

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Haukeland University Hospital Bergen Hordaland Norway 5021

    Sponsors and Collaborators

    • Haukeland University Hospital
    • Norwegian School of Sport Sciences
    • Oslo University Hospital

    Investigators

    • Principal Investigator: Tiina M Andersen, PhD, Department of Physiotherapy, Haukeland University Hospital, Bergen, Norway

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Haukeland University Hospital
    ClinicalTrials.gov Identifier:
    NCT03947112
    Other Study ID Numbers:
    • 2019/260
    First Posted:
    May 13, 2019
    Last Update Posted:
    Dec 29, 2021
    Last Verified:
    Nov 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Haukeland University Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 29, 2021