Testing a Tailored Home Exercise Program to Reduce Pain and Fatigue in Patients with FSHD.

ConditionFSHD
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorRadboud University Medical Center

About this trial

The goal of this intervention study is to determine the effect of a tailored exercise program (with aerobic, strength and balance training) in patients with FSHD.

The main aim is to determine the effect of the exercise program on pain and fatigue.

Participants will follow a 16 week training program with tailored exercises. The exercises will be prescribed via the app 'Physitrack'. After 16 weeks, the effect on pain, fatigue, fatigability, aerobic capacity, balance, physical function, sleep and the ability to participate in social activities will be determined.

Eligibility criteria

Qualifiers

Age >18 years

Verified diagnosis of FSHD type 1, based on the clinical criteria established by Padberg et al. (1991) (22).

Category A or B of the four clinical categories according to the Comprehensive Clinical Evaluation Form (23), these patients have the most peculiar signs of the disease

A CIS-fatigue score of ≥ 35

Disqualifiers

Use of beta-blocker medication

Presence of additional diseases likely to interfere with the measurements

Psychological-psychiatric disorders

A musculoskeletal injury that impairs exercising

Trial design

Treatments tested in this trial

  • Personalised Exercise
  • Historical control group

Treatment groups

50 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Radboud University Medical Center

Lead sponsor

Università di Pavia

Collaborator