PediatricsNeuromuscular RehabilitationAdvanced LevelProfessionals
Duchenne Muscular Dystrophy: Safe Activity, Monitoring and Function
A family-centered framework for activity, range management, functional monitoring and coordinated care in Duchenne muscular dystrophy.
15 October 20269 min readEvidence sources included
What You Should Be Able to Explain After Reading
- Describe physiotherapy priorities across stages of DMD.
- Select functional, range and participation measures.
- Support activity without excessive fatigue or overwork.
- Recognize changes requiring specialist review.
Condition framework
DMD is a progressive X-linked neuromuscular condition associated with loss of dystrophin. Function and risks change over time, so care should be coordinated with a specialist neuromuscular team.
Physiotherapy supports comfortable range, safe mobility and participation, contracture-risk management and early recognition of change; it does not reverse the underlying disease.
Assessment and monitoring
- Review walking, transfers, stairs, falls, fatigue, pain, school participation, sleep, orthoses, equipment and family goals. Ask about recent decline rather than assuming every change is gradual progression.
- Use stage-appropriate measures agreed with the specialist team, such as the North Star Ambulatory Assessment, timed tasks, range records and participation reports.
- Coordinate respiratory, cardiac, orthopedic and bone-health surveillance. New breathlessness, chest pain, syncope, rapid functional decline or suspected fracture warrants prompt medical review.
Activity and exercise reasoning
- Encourage enjoyable, individualized submaximal activity when medically appropriate. Avoid prolonged inactivity, exhausting sessions and high-load eccentric work that causes marked pain or prolonged weakness.
- A programme may use short bouts of low-to-moderate effort movement, gentle active-assisted range and functional tasks with planned rest. Dose must be individualized; generic resistance prescriptions are not suitable for every stage.
- Use positioning, comfortable range routines, orthoses or adaptive equipment when indicated. Do not force painful stretching.
Progression and family partnership
- Monitor symptoms during activity and recovery later that day and the next day. Reduce load if fatigue is disproportionate, pain persists or function worsens.
- Progress participation, movement quality or duration conservatively, changing one variable at a time. Co-design goals with the child and family and coordinate with school and the multidisciplinary team.
- Do not attribute temporary decline solely to disease progression without considering injury, illness, pain, sleep or cardiopulmonary change. Good rehabilitation is proactive, coordinated and adaptable.
Evidence & Further Reading
These sources are provided so learners can trace the clinical recommendations and read the original guidance.