Effects of a 12-week Strength Training Program in Women With Myotonic Dystrophy Type 1

February 7, 2023 updated by: Élise Duchesne, Université de Sherbrooke
20 women with myotonic dystrophy type 1 (DM1) will complete a 12-week lower-limb strength training program. The training program consist of 3 series of 6 to 8 maximal repetitions of 5 different exercises: Leg extension, leg press, hip abduction, squat and plantar flexion. Training sessions will be closely supervise and take place twice a week. It is hypothesize that the training program will induce muscular hypertrophy despite the genetic defect. The training program should also have positive effects on function. The participants will be evaluated at baseline, week 6, week 12, month 6 and month 9 to quantify the effects of the training program and if these effects will be maintained over time.

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

12

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Quebec
      • Saguenay, Quebec, Canada, G7X 7X2
        • Groupe de recherche interdisciplinaire sur les maladies neuromusculaires

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

30 years to 65 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • DM1 diagnosis must be confirmed by genetic analysis;
  • Women sex, aged between 30 and 65 years old;
  • Be able to walk without assistance;
  • Consent of the neurologist must be given to participate in this study;
  • Must reside in the Saguenay-Lac-St-Jean region;
  • Subjects must be able to give their consent freely and voluntarily.

Exclusion Criteria:

  • Patients with any other form of muscular dystrophy are excluded;
  • Any contraindication for strenuous exercise or muscle biopsy.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: SUPPORTIVE_CARE
  • Allocation: NA
  • Interventional Model: SEQUENTIAL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Training program
12-week strength training program of the lower limbs consisting of 5 different exercises: Leg extension, leg press, hip abduction, squat and plantar flexion. All exercises will be perform between 6 and 8 maximal repetitions.
12-week strength training program of the lower limbs consisting of 5 different exercises: Leg extension, leg press, hip abduction, squat and plantar flexion. All exercises will be perform between 6 and 8 maximal repetitions.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in maximal isometric muscle strength of the knee extensors
Time Frame: At baseline, week 6, week 12, month 3 and month 6
Changes in maximal isometric muscle strength of the knee extensors measure by quantify muscle testing using a handheld dynamometer
At baseline, week 6, week 12, month 3 and month 6

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in 1-repetition maximum strength of the leg extension exercise
Time Frame: At baseline, week 6 and week 12
Changes in 1-repetition maximum strength of the leg extension exercise
At baseline, week 6 and week 12
Changes in 1-repetition maximum strength of the leg press exercise
Time Frame: At baseline, week 6 and week 12
Changes in 1-repetition maximum strength of the leg press exercise
At baseline, week 6 and week 12
Changes in 1-repetition maximum strength of the hip abduction exercise
Time Frame: At baseline, week 6 and week 12
Changes in 1-repetition maximum strength of the hip abduction exercise
At baseline, week 6 and week 12
Changes in 1-repetition maximum strength of the squat exercise
Time Frame: At baseline, week 6 and week 12
Changes in 1-repetition maximum strength of the squat exercise
At baseline, week 6 and week 12
Changes in comfortable walking speed in the 10-meter walk test
Time Frame: At baseline, week 6, week 12, month 6 and month 9
Changes in comfortable walking speed in the 10-meter walk test
At baseline, week 6, week 12, month 6 and month 9
Changes in maximal walking speed in the 10-meter walk test
Time Frame: At baseline, week 6, week 12, month 6 and month 9
Changes in maximal walking speed in the 10-meter walk test
At baseline, week 6, week 12, month 6 and month 9
Changes in the number of repetitions in the 30-seconds sit-to-stand test
Time Frame: At baseline, week 6, week 12, month 6 and month 9
Changes in the number of repetitions in the 30-seconds sit-to-stand test
At baseline, week 6, week 12, month 6 and month 9
Changes in the score of the lower extremity functional scale
Time Frame: At baseline, week 12, month 6 and month 9
Changes in the score of the lower extremity functional scale (LEFS). The LEFS is an 80-point questionnaire with 20 items scored from 0 to 4. A score of 80 means no disfunction while a score of 0 means maximal disfunction.
At baseline, week 12, month 6 and month 9
Changes in the score of the myotonic dystrophy health index
Time Frame: At baseline, week 6, week 12, month 6 and month 9
Changes in the score of the myotonic dystrophy health index (MDHI). The MDHI is a 114-item questionnaire scored from 0 to 100, where 0 means no disability and 100 means maximal disability.
At baseline, week 6, week 12, month 6 and month 9
Changes in the score of the Fatigue and Daytime Sleepiness Scale
Time Frame: At baseline, week 6, week 12, month 6 and month 9
Changes in the score of the Fatigue and Daytime Sleepiness Scale (FDSS). The FDSS is a 12-item questionnaire where all questions are scored from 0 to 2. A higher score means more daytime sleepiness and fatigue.
At baseline, week 6, week 12, month 6 and month 9
Changes in the Marin apathy scale
Time Frame: At baseline, week 12, month 6 and month 9
Changes in the Marin apathy scale. The Marin apathy scale is scored by the clinician where he interviews the subject and then scores an 18-item list on a scale of 1 to 4. A high score means more apathy.
At baseline, week 12, month 6 and month 9
Changes in the Hospital Anxiety and Depression Scale
Time Frame: At baseline, week 6, week 12 and month 6
Changes in the Hospital Anxiety and Depression Scale (HADS). The HADS is a 14-item questionnaire with a scale from 0 to 3 for each item. A high score means high depression and anxiety.
At baseline, week 6, week 12 and month 6
Changes in muscle biopsy of the vastus lateralis: muscle fiber typing
Time Frame: At baseline and week 12
Changes in muscle biopsy of the vastus lateralis: muscle fiber typing
At baseline and week 12
Changes in muscle biopsy of the vastus lateralis: muscle fiber size
Time Frame: At baseline and week 12
Changes in muscle biopsy of the vastus lateralis: muscle fiber size (smallest diameter of the fiber)
At baseline and week 12
Changes in muscle biopsy of the vastus lateralis: muscle proteomics
Time Frame: At baseline and week 12
Changes in muscle biopsy of the vastus lateralis: muscle proteomics (protein expression)
At baseline and week 12
Changes in muscle biopsy of the vastus lateralis: muscle transcriptomics
Time Frame: At baseline and week 12
Changes in muscle biopsy of the vastus lateralis: muscle transcriptomics (RNA expression analysis)
At baseline and week 12
Changes in muscle biopsy of the vastus lateralis: mitochondrial function
Time Frame: At baseline and week 12
Changes in muscle biopsy of the vastus lateralis: mitochondrial function. Analysis of mitochondrial markers and enzymes
At baseline and week 12
Changes in muscle biopsy of the vastus lateralis: Nuclear foci
Time Frame: At baseline and week 12
Changes in muscle biopsy of the vastus lateralis: Nuclear foci (changes in accumulation of nuclear foci)
At baseline and week 12
Changes in maximal isometric muscle strength of the knee flexors
Time Frame: At baseline and week 12
Changes in maximal isometric muscle strength of the knee flexors measure by quantify muscle testing using a handheld dynamometer
At baseline and week 12
Changes in maximal isometric muscle strength of the hip flexors
Time Frame: At baseline and week 12
Changes in maximal isometric muscle strength of the hip flexors measure by quantify muscle testing using a handheld dynamometer
At baseline and week 12
Changes in maximal isometric muscle strength of the hip extensors
Time Frame: At baseline and week 12
Changes in maximal isometric muscle strength of the hip extensors measure by quantify muscle testing using a handheld dynamometer
At baseline and week 12
Changes in maximal isometric muscle strength of the hip abductors
Time Frame: At baseline and week 12
Changes in maximal isometric muscle strength of the hip abductors measure by quantify muscle testing using a handheld dynamometer
At baseline and week 12
Changes in maximal isometric muscle strength of the ankle dorsiflexors
Time Frame: At baseline and week 12
Changes in maximal isometric muscle strength of the ankle dorsiflexors measure by quantify muscle testing using a handheld dynamometer
At baseline and week 12
Changes in maximal isometric grip strength
Time Frame: At baseline and week 12
Changes in maximal isometric muscle strength of prehension measure by quantify muscle testing using a hand grip dynamometer
At baseline and week 12
Changes in the time to perform of the Timed Up and Go
Time Frame: At baseline, week 6, week 12, month 6 and month 9
Changes in the time to perform of the Timed Up and Go
At baseline, week 6, week 12, month 6 and month 9
Changes in the time to perform the Timed stair test
Time Frame: At baseline, week 6, week 12, month 6 and month 9
Changes in the time to perform the Timed stair test
At baseline, week 6, week 12, month 6 and month 9
Change in the score of the Brief Pain Inventory
Time Frame: At baseline, week 6, week 12, month 6 and month 9
Change in the score of the Brief Pain Inventory. The Brief Pain Inventory is a self-administer test that asses the dimensions of pain such as intensity of pain, functional incapacities, social and family repercussions, and psychological distress.
At baseline, week 6, week 12, month 6 and month 9
Self-perceived changes in daily life
Time Frame: At week 12
Self-perceived changes in daily life
At week 12
Change in the number of falls
Time Frame: At baseline, week 12, month 6 ans month 9
Number of falls in the last week and in the last month
At baseline, week 12, month 6 ans month 9
Change in score of the DM1-Activ questionnaire
Time Frame: At baseline, week 6, week 12, month 6 ans month 9
Change in score of the DM1-Activ questionnaire. This questionnaire asses activity and social participation with DM1 population. It contains 20 items with a maximal socre of 40 points, a lower score represent a bigger impact of the disease on activities and social participation.
At baseline, week 6, week 12, month 6 ans month 9
Change in blood : biochemical markers (CK, Protein C reactive, leukocytes, cytokines, etc.)
Time Frame: At baseline and week 12
Change in blood : biochemical markers (CK, Protein C reactive, leukocytes, cytokines, etc.)
At baseline and week 12
Change in urine sample : exercise biomarkers (-Omics markers)
Time Frame: At baseline and week 12
Change in urine sample : exercise biomarkers (-Omics markers)
At baseline and week 12
Change in saliva sample : exercise biomarkers (-Omics markers)
Time Frame: At baseline and week 12
Change in saliva sample : exercise biomarkers (-Omics markers)
At baseline and week 12
Change of the center of pressure (COP) measure in static posturography : open eyes bipodal position
Time Frame: At baseline, week 6, week 12, 6 months and 9 months
Change of the center of pressure (COP) in static posturography : open eyes bipodal position
At baseline, week 6, week 12, 6 months and 9 months
Change of the center of pressure (COP) measure in static posturography : closed eyes bipodal position
Time Frame: At baseline, week 6, week 12, 6 months and 9 months
Change of the center of pressure (COP) in static posturography : closed eyes bipodal position
At baseline, week 6, week 12, 6 months and 9 months
Change of the center of pressure (COP) measure in static posturography : open eyes semi-tandem position
Time Frame: At baseline, week 6, week 12, 6 months and 9 months
Change of the center of pressure (COP) in static posturography : open eyes semi-tandem position
At baseline, week 6, week 12, 6 months and 9 months
Change of the center of pressure (COP) measure in static posturography : open eyes tandem position
Time Frame: At baseline, week 6, week 12, 6 months and 9 months
Change of the center of pressure (COP) in static posturography : open eyes tandem position
At baseline, week 6, week 12, 6 months and 9 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

January 1, 2022

Primary Completion (ACTUAL)

June 30, 2022

Study Completion (ACTUAL)

January 10, 2023

Study Registration Dates

First Submitted

May 24, 2022

First Submitted That Met QC Criteria

May 30, 2022

First Posted (ACTUAL)

June 1, 2022

Study Record Updates

Last Update Posted (ACTUAL)

February 10, 2023

Last Update Submitted That Met QC Criteria

February 7, 2023

Last Verified

February 1, 2023

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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