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Clinical Trials/NCT06716931
NCT06716931
Recruiting
Not Applicable

Investigating Benefits of A Physical Therapist (PT)-Guided Exercise Program in Myotonic Dystrophy Type 2 (DM2)

Massachusetts General Hospital2 sites in 1 country24 target enrollmentMarch 4, 2025
InterventionsExercise

Overview

Phase
Not Applicable
Intervention
Exercise
Conditions
Myotonic Dystrophy 2
Sponsor
Massachusetts General Hospital
Enrollment
24
Locations
2
Primary Endpoint
Manual Muscle Test (MMT)
Status
Recruiting
Last Updated
17 days ago

Overview

Brief Summary

An exercise regimen (PRIME: Proximal Resistance In-House Movement Exercise) has been designed for patients with myotonic dystrophy type 2 (DM2). The hypothesis is that this patient-friendly physical therapist (PT)-guided exercise program associates with improved functional capacity and muscle composition in DM2 in this two-period two-sequence cross-over study. Thus, participant will be randomized to one of the three possible groups. Participants in GROUP A will perform exercise routine virtually under the direct supervision of a physical therapist once a week and another session on their own for the first three months, then they will continue with same exercise routine at home for the last 3 months on their own. Participants in GROUP B will perform exercise routine virtually under the direct supervision of a physical therapist twice a week for the first three months, then they will continue with same exercise routine at home for the last 3 months on their own. Participants in GROUP C will perform exercise routine on their own during the first 3 months, then they will perform exercise routine virtually under the direct supervision of a physical therapist. Each group will include around 8 participants. Duration of the study is 6 months. In addition to exercise sessions, participants will have evaluation of their strength, motor function and muscle composition at three time points: initiation, 3 months and completion of the study at 6 months. Muscle composition will be assessed by electrical impedance myography which is a portable, non-invasive, painless and non-radiation tool that applies a weak high multifrequency electrical current to the examined muscle and allows to obtain information about its composition.

Registry
clinicaltrials.gov
Start Date
March 4, 2025
End Date
March 1, 2028
Last Updated
17 days ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Paloma Gonzalez Perez, MD, PhD

Neurologist

Massachusetts General Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients with genetically confirmed myotonic dystrophy 2 (DM2) who are ≥18 and ≤ 70 years old.
  • Patients are ambulatory without need of any assistance or device.
  • Patients have a normal ECG within the 3 months prior to Screening visit (of note, patients with DM2 are recommended to have routine ECG as part of patient care. So, this ECG will be done as part of patient care).
  • Body mass index (BMI) ≥20 and ≤30.

Exclusion Criteria

  • Subjects younger than 18 years old or older than 70 years old.
  • Inability or unwillingness of the subject to give written informed consent.
  • Subjects with pacemaker.
  • Blood pressure \<90/50 mmHg or \>160 mmHg/90 mmHg at Screening visit
  • Resting heart rate of \<60 or \>100 beats/minute at Screening visit.
  • Any fall within the last six months.
  • Any history of syncopal episodes or family history of sudden death.
  • Patients who are pregnant or plan to become pregnant. A urine pregnancy test will be performed at visit 1 and 3 for women of childbearing age. If positive or if subject is planning to become pregnant, subject will be not eligible for the study.

Arms & Interventions

Group A

Exercise under the supervision of physical therapist in clinic during the first 3 months, then self-directed exercise routine for the last 3 months

Intervention: Exercise

Group B

Exercise under the supervision of physical therapist virtually during the first 3 months, then self-directed exercise routine for the last 3 months

Intervention: Exercise

Group C

Self-directed exercise routine for the first 3 months, then exercise routine under the supervision of physical therapist virtually during the last 3 months

Intervention: Exercise

Outcomes

Primary Outcomes

Manual Muscle Test (MMT)

Time Frame: From enrollment to the end of treatment at 6 months

Score of manual muscle strength test scale. This is a strength exam at bedside of muscle groups

Six-minute walking test

Time Frame: From enrollment to the end of treatment at 6 months

Distance in meters that subject can walk in six minutes

Secondary Outcomes

  • Quantitative myometry(From enrollment to the end of treatment at 6 months)
  • Muscle resistance/reactance measures in ohms(From enrollment to the end of treatment at 6 months)

Study Sites (2)

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