- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02650882
Effect of Inspiratory Muscle Training on the Performance of Handball Athletes
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The study was designed to evaluate the effects of a 12-week IMT program on the respiratory muscle strength and aerobic physical performance of handball players. Nineteen male athletes took part in the study, divided into the experimental group (EG), which took part in the evaluations, maintained their regular sporting activities and carried out the IMT (n=10), and the placebo group (PG), which took part in the evaluations, maintained their regular sporting activities and carried out an IMT with a load considered to be placebo (n=09), Experimental procedures were carried out by trained researchers and a qualified team. The evaluations and IMT were carried out during the competitive season, the training frequency being based on the competition program, following the traditional annual model.
The athletes were submitted to an initial evaluation composed of measuring the respiratory muscle strength (RMS) using a manovacuometer, and an evaluation of the aerobic physical performance carried out using the cardiopulmonary exercise test (CPET).
The athletes were reevaluated after 12 weeks for subsequent analysis and comparison with the initial values.
All the subjects were previously informed about the experimental procedures, and signed a free and clarified term of consent. The project was approved by the Ethics in Research Committee of the Institution with the number 62/13.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
GENDER: Male
AGE LIMITS:
Minimum age: 18 years Maximum age:30 years Accepts Healthy Volunteers? YES
Eligibility Criteria
Inclusion criteria:
- male gender
- competition level athlete for at least one year
- regularly takes part in the training sessions
Exclusion criteria:
- smoke
- shows signs of respiratory and/or cardiovascular diseases
- use supplements and/or medication that influences physical performance
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Placebo Comparator: placebo
Placebo group (PG) Nine athletes who maintained their regular sporting activities and were submitted to the IMT program for 12 weeks with a fixed load at 15% MIP, placebo protocol.
|
|
|
Experimental: Experimental
Experimental group (EG) Ten athletes who maintained their regular sporting activities and were submitted to the IMT program for 12 weeks with a progressive load at 60%, 70% and 80 % of MIP.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Effect of inspiratory muscle training on the respiratory muscle strength performed using a manometer and measured with cmH20
Time Frame: Finalized study (24 weeks)
|
The evaluation of respiratory muscle strength (RMS) was performed using a manometer and measured with cmH20
|
Finalized study (24 weeks)
|
|
Effect of inspiratory muscle training on the muscular respiratory resistance evaluated by maximum voluntary ventilation (MVV) carried out with a spirometer
Time Frame: Finalized study (24 weeks)
|
The muscular respiratory resistance was evaluated by maximum voluntary ventilation (MVV) carried out with a spirometer
|
Finalized study (24 weeks)
|
|
Effect of inspiratory muscle training on the aerobic physical performance (PP) using cardiopulmonary test (CPT), and measured by VO2max
Time Frame: Finalized study (24 weeks)
|
The evaluation of aerobic performance was carried out using cardiopulmonary test (CPT), and measured by VO2max
|
Finalized study (24 weeks)
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 62/13
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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