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Clinical Trials/NCT03947112
NCT03947112
Completed
N/A

Physical Activity Level of Norwegian Boys with Duchenne Muscular Dystrophy - a Cross Sectional Study

Haukeland University Hospital1 site in 1 country28 target enrollmentAugust 20, 2020

Overview

Phase
N/A
Intervention
Not specified
Conditions
Duchenne Muscular Dystrophy
Sponsor
Haukeland University Hospital
Enrollment
28
Locations
1
Primary Endpoint
Physical activity registration
Status
Completed
Last Updated
last year

Overview

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.

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.

Registry
clinicaltrials.gov
Start Date
August 20, 2020
End Date
June 30, 2021
Last Updated
last year
Study Type
Observational
Sex
Male

Investigators

Sponsor
Haukeland University Hospital
Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

Physical activity registration

Time Frame: 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 Outcomes

  • Leisure time physical activity(Day 1)
  • Self-Reported Questionnaire(Day 1)

Study Sites (1)

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