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Safety and Effectiveness of Resistance Exercise Training in Patients With Pompe Disease.

Safety and Effectiveness of Resistance Exercise Training in Patients With Late Onset Pompe Disease- A Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02654886
Acronym
ExercisPompe
Enrollment
10
Registered
2016-01-13
Start date
2015-10-31
Completion date
2019-09-24
Last updated
2019-09-26

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

Conditions

Muscle Weakness, Pompe Disease

Keywords

exercise, Pompe disease, Pompe

Brief summary

The purpose of this research study is to determine if exercise will help improve muscle strength, endurance, and quality of life in individuals with Pompe disease. This is a research study to further define the outcome of patients with Pompe disease treated with a combined diet and exercise therapy.

Detailed description

Eligibility: Subjects that are age 16 years or older, have been diagnosed with Pompe disease by genetic testing, and are showing symptoms such as muscle weakness Time Commitment: The study will last for 8 months. This study consists of a baseline visit of and return visits at week 9, week 16, week 24, and week 32. At the week 9 visit the subject will be given an individualized exercise plan which will be carried out over the next 24 weeks. The subject will be asked to return for three more visits at week16, week 24 and week 32. The 24 week training period will involve 3 workouts a week approximately 15-30 minutes each. It will also involve a breathing exercise that the subject can do at home twice daily for 10-15 minutes per session. The study visits will include the exercise plan, physical exam, blood draw and questionnaires. Anticipated Benefits: The possible benefits include a delay in progression of muscle weakness. The knowledge gained from this study will help researchers understand the effect of exercise on the disease. This may eventually lead to new forms of prevention of symptom onset in the future.

Interventions

OTHERResistance Exercise Training

Resistance Exercise Training: knee extension and elbow flexion each 3 times per week 3 sets each session; 10 reps/set for 6 months Respiratory muscle strength training: 25 repetitions -twice daily, 6 days/week for 6 months

Sponsors

University of California, Irvine
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
16 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Able to fully consent to the protocol. 2. Physically able to perform resistance exercises for 12 weeks. 3. Patients with a confirmed diagnosis of Pompe disease. 4. Age 16 years to 75 years. 5. Currently receiving ERT. 6. Patient on ERT for at least 1year.

Exclusion criteria

1. Patients with no confirmed diagnosis of Pompe disease, either by GAA enzyme deficiency from any tissue and/or molecular testing revealing two GAA gene mutations 2. Unable to walk or cycle 3. Unable to consent to the study/ procedures 4. Women who are pregnant or breastfeeding 5. Heart disease 6. Patients with any metal inside their body such as metallic clips used for vascular repairs and/or implanted devices such as cardiac pacemakers which would prevent them from doing the MRI.

Design outcomes

Primary

MeasureTime frame
Isometric muscle strength change from week 8 through week 32Eight months

Secondary

MeasureTime frame
6 Minute Walk Test change from week 8 through week 32Eight months
Maximum Inspiratory Pressures percent change from week 8 through week 32Eight months
MRC score change from week 8 through week 32Eight months
Muscle volume and texture change from week 8 through week 32 using MR ImagingEight months
Glycogen content change in quadriceps muscle from week 8 through week 32Eight months
GAA enzyme activity change from week 8 through week 32Eight months
HEX4 change from week 8 through week 32Eight months
Other spirometry parameters change from week 8 through week 32Eight months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026