Home rehabilitation program for patients with muscular dystrophies

Rehabilitation in Muscular Dystrophies From the Hospital Facility to the Home: Pilot Project

Not applicable Interventional IRCCS Eugenio Medea · NCT06378203

This study tests a home rehabilitation program for people with muscular dystrophies to see if personalized exercise plans and remote support from physiotherapists can help improve their strength and well-being.

Quick facts

PhaseNot applicable
Study typeInterventional
Enrollment10 (estimated)
Ages18 Years and up
SexAll
SponsorIRCCS Eugenio Medea Academic / other
Locations1 site (Bosisio Parini, Lecco)
Trial IDNCT06378203 on ClinicalTrials.gov

What this trial studies

This project aims to provide a tele-rehabilitation program for patients with muscular dystrophies, focusing on continuity of care from hospital to home. It involves creating personalized therapeutic plans that patients can follow independently at home, supported by remote monitoring from physiotherapists. The program includes 15 training sessions to enhance muscle strength and endurance, while also addressing psychological well-being. The effectiveness of this approach will be evaluated over a 6-month period.

Who should consider this trial

Good fit: Ideal candidates are individuals with a confirmed genetic diagnosis of specific types of muscular dystrophies who can walk independently in a protected environment.

Not a fit: Patients with severe cardiac or respiratory conditions may not benefit from this rehabilitation program.

Why it matters

Potential benefit: If successful, this program could significantly improve the quality of life and physical capabilities of patients with muscular dystrophies.

How similar studies have performed: Previous studies have shown positive outcomes with tele-rehabilitation approaches for similar conditions, indicating potential for success in this pilot project.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:- definite genetic diagnosis of Limb Girdle Muscular Dystrophy: LGMD2A/R1(calpain 3 deficiency), LGMD2B/R2(dysferlin deficiency), LGMD2I/R9 (FKRP), LGMD2L /R11(ANOCTAMIN 5) or Facio Scapulo Humeral Dystrophy (FSHD) or Becker muscular dystrophy (BMD);

* strength values at the level of the main antigravity muscles \> or equal to 3, according to the Medical Research Council (MRC) scale;
* independent walking in a protected (internal) environment, even with assistance;
* patients must have performed at least 1 clinical-functional evaluation at our facility in the year preceding the start of the trial.
* They must express compliance with joining the project and must not be followed from a physiotherapeutic point of view elsewhere during the 6 months of participation in the project.

Exclusion Criteria:

* dilated or ischemic heart disease with Left Ventricle Ejection Fraction \<50%;
* chronic respiratory failure with Forced Vital Capacity \< 40% predicted, nocturnal oxygen desaturation - \> 5% of nocturnal time spent with peripheral oxygen saturation levels \< 90).

Where this trial is running

Bosisio Parini, Lecco

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Muscular DystrophiesLimb Girdle Muscular DystrophyFacio-Scapulo-Humeral DystrophyBecker Muscular Dystrophymuscular dystrophymuscular trainingmuscular exercisetele monitoring
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.