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Gamified Occupational Therapy for Adolescents With Duchenne Muscular Dystrophy

Gamified Occupational Therapy for Adolescents With Duchenne Muscular Dystrophy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06402942
Acronym
DMD
Enrollment
20
Registered
2024-05-07
Start date
2025-05-01
Completion date
2026-12-08
Last updated
2026-01-27

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

Conditions

Duchenne Muscular Dystrophy, Gamification, Occupational Therapy

Brief summary

This research aims to improve the quality of life, occupational performance, occupational satisfaction and emotional health of young people with Duchenne muscular dystrophy compared to the classical occupational therapy program. The findings are planned to shed light on the development of new and effective strategies in the rehabilitation of adolescents with Duchenne muscular dystrophy.

Interventions

OTHERGamified occupational therapy programme

Gamified occupational therapy program for the experimental group and classical occupational therapy program for the control group, which will be applied to both groups for eight weeks

OTHERClassic occupational therapy programme

Gamified occupational therapy program for the experimental group and classical occupational therapy program for the control group, which will be applied to both groups for eight weeks

Sponsors

Başak Çağla Arslan
Lead SponsorOTHER_GOV
Hacettepe University
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Randomised control trial

Eligibility

Sex/Gender
MALE
Age
13 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Being diagnosed with Duchenne muscular dystrophy * To be literate in Turkish * To have scored 27 points or more on the Modified Mini Mental Test * Having a computer, tablet and internet connection * Volunteering to participate in the study by their parents and reading and signing the informed consent form

Exclusion criteria

* Having a neurological disease other than Duchenne muscular dystrophy and/or another diagnosed neurological disease accompanying Duchenne muscular dystrophy * Having a cooperation problem that prevents completing the assessments for any reason * Difficulty understanding and speaking the Turkish language

Design outcomes

Primary

MeasureTime frameDescription
Demographic information formAt the start of the evaluations
Modified Mini Mental State Testbefore and after the eight-week intervention programs
Vignos lower extremity functional scalebefore and after the eight-week intervention programsThis scale was developed to assess the level of ambulation in neuromuscular diseases and consists of 10 stages. In this scale, the ambulation level of the person decreases from the first stage to the tenth stage.
Brooke upper extremity functional classification scalebefore and after the eight-week intervention programsThis scale was developed to assess the functional levels of the upper extremity in neuromuscular diseases and consists of 6 stages. In this scale, progression from the first stage to the sixth stage indicates a decrease in the functionality of the upper extremity.
The Pediatric Quality of Life Inventory 3.0 Neuromuscular Modulebefore and after the eight-week intervention programs
Canadian Occupational Performance Measurebefore and after the eight-week intervention programs
Children's Depression Inventorybefore and after the eight-week intervention programsConsisting of 27 items and using a 3-point Likert-type scale, this scale assesses the depression levels of children between the ages of 6-17. The total score of the scale, which measures the emotional state in the last 2 weeks, is 54 and the severity of depression increases as the total score increases. The cut-off value of the scale was determined as 19 points.
The Pediatric Quality of Life Inventory Multidimensional Fatigue Scalebefore and after the eight-week intervention programsThis scale consists of 18 items and 3 subsections: general fatigue (6 items), fatigue during sleep/rest (6 items) and cognitive fatigue (6 items). Separate scores can be calculated for each subsection and the total score is obtained by summing the scores obtained from these sections. High scores indicate low fatigue.
The Numeric Rating Scale - Painbefore and after the eight-week intervention programsThis scale uses a 10-centimeter line. The left beginning of the line represents "no pain" (0 points) and the end of the line represents "excruciating pain" (10 points).

Countries

Turkey (Türkiye)

Contacts

CONTACTBaşak Çağla Arslan, Master Degree
ptbasakc@gmail.com4448548

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 31, 2026