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Investigating Exercise in Myotonic Dystrophy Type 2 (DM2)

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06716931
Acronym
DM2
Enrollment
24
Registered
2024-12-04
Start date
2025-03-04
Completion date
2028-03-01
Last updated
2026-04-15

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

Conditions

Myotonic Dystrophy 2

Keywords

exercise, physical therapist, myotonic dystrophy type 2, electrical impedance myography

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.

Interventions

OTHERExercise

A patient-friendly exercise routine has been designed for patients with myotonic dystrophy type 2. Benefits of this exercise regimen in different settings (at home versus clinic, self-directed versus physical therapist-directed) will be investigated. In person exercise supervised by physical therapist and then self-directed exercise in Group A

Sponsors

Massachusetts General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Manual Muscle Test (MMT)From enrollment to the end of treatment at 6 monthsScore of manual muscle strength test scale. This is a strength exam at bedside of muscle groups
Six-minute walking testFrom enrollment to the end of treatment at 6 monthsDistance in meters that subject can walk in six minutes

Secondary

MeasureTime frameDescription
Quantitative myometryFrom enrollment to the end of treatment at 6 monthsMuscle dynamometry of different muscle groups measured in kilograms
Muscle resistance/reactance measures in ohmsFrom enrollment to the end of treatment at 6 monthsusing electrical impedance myography, resistance and reactance measures in ohms will be obtained simultaneously from each examined muscle

Countries

United States

Contacts

CONTACTZoe Sheitman, DPT
zsheitman@mgh.harvard.edu617-726-3642

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 16, 2026