Gamified occupational therapy program for adolescents with Duchenne muscular dystrophy: A study protocol for randomized controlled trial.
Başak Çağla Arslan, Sedef Şahin
https://pubmed.ncbi.nlm.nih.gov/42530145/Actively Recruiting
Led by Başak Çağla Arslan · Updated on 2026-01-27
20
Participants Needed
1
Research Sites
15 weeks
Total Duration
Researchers are evaluating the impact of a gamified occupational therapy program compared to the classic occupational therapy program on adolescents with Duchenne muscular dystrophy. The study aims to improve quality of life, occupational performance, satisfaction, and emotional health in young people with this condition. The findings hope to guide the development of new rehabilitation strategies for this group. Participants are randomly assigned to one of two groups the experimental group receiving the gamified occupational therapy program or the control group receiving the classical occupational therapy program. Both interventions are applied over an eight-week period. These therapy programs are designed to support adolescents in managing the challenges of Duchenne muscular dystrophy. During the study, participants will complete several assessments before and after the eight-week intervention, including functional scales for upper and lower extremities, quality of life inventories, depression and fatigue scales, and pain ratings. Demographic information and cognitive function tests will also be collected at the start. The study runs from May 2025 to December 2026, providing a structured evaluation of the therapy effects.
CONDITIONS
Gamified Occupational Therapy for Adolescents With Duchenne Muscular Dystrophy
B
Başak Çağla Arslan, Master Degree
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Başak Çağla Arslan
Lead Sponsor
Hacettepe University
Collaborating Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 8 weeks
Participants receive either a gamified occupational therapy programme or a classic occupational therapy programme for eight weeks.
Assessments before and after the intervention period
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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Başak Çağla Arslan, Sedef Şahin
https://pubmed.ncbi.nlm.nih.gov/42530145/Başak Çağla Arslan
Lead Sponsor
Hacettepe University
Collaborating Sponsor