Effect of Respiratory Muscle Training in Multiple Sclerosis
Not Applicable
Recruiting
- Conditions
- Multiple Sclerosis.Multiple sclerosis
- Registration Number
- IRCT20200827048542N1
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 36
Inclusion Criteria
Definite diagnosed relapsing-remitting MS
Year after diagnosed at least one year
Be able to walk without support at least 10 meters
Not have an relapse at least one month
Taking no intravenous corticosteroid drug
Exclusion Criteria
history of any respiratory disease
have an active pulmonary infection
Contraindicated for aerobic activity (such as orthopedic and muscular problem)
smoker
pregnancy
Participate in another research program
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Maximum Inspiratory Pressure. Timepoint: before intervention and 8 weeks after intervention. Method of measurement: Body Box machine.;Maximum Expiratory Pressure. Timepoint: before intervention and 8 weeks after intervention. Method of measurement: Body Box machine.
- Secondary Outcome Measures
Name Time Method Quality of Life. Timepoint: before intervention and 8 weeks after intervention. Method of measurement: SF-36 questionnaire.;Aerobic capacity. Timepoint: before intervention and 8 weeks after intervention. Method of measurement: Six Minute Walk Test (6MWT).;Functional capacity. Timepoint: before intervention and 8 weeks after intervention. Method of measurement: Timed Up and Go test (TUG).;Forced Expiratory volume in the first second (FEV1). Timepoint: before intervention and 8 weeks after interventio. Method of measurement: Spirometry.;Forced Expiratory volume in the first second (FEV1)/Forced Vital Capacity (FVC). Timepoint: before intervention and 8 weeks after intervention. Method of measurement: Spirometry.;Fatigue. Timepoint: before intervention and 8 weeks after intervention. Method of measurement: Modified Fatigue Impact Scale questionnaire (MFIS).