Effect of a Modified Respiratory Rehabilitation Program on Exercise-Induced Forced Expiratory Volume for 1 second Decline in Long-Distance Runners with Exercise-Induced Bronchospasm: A Randomized Controlled Trial
Overview
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Enrollment
- 62
- Locations
- 1
- Primary Endpoint
- decline percentage of forced expiratory volume for 1 second
Overview
Brief Summary
This randomized controlled trial evaluates the effectiveness of a 5-week Modified Respiratory Rehabilitation Program compared to standard aerobic exercise in improving lung function and exercise tolerance in long-distance runners with Exercise-Induced Bronchospasm. The study targets 146 participants aged 18-45 years who are actively training long-distance runners experiencing at least 10 percent decline in Forced Expiratory Volume in 1 second after exercise challenge. Participants will be randomly assigned to either the intervention group receiving Modified Respiratory Rehabilitation, including High-Intensity Interval Respiratory Training, breathing pattern optimization, and sport-specific running protocols, or the control group receiving standard aerobic exercise training. Both groups will undergo supervised 5-week programs conducted by qualified physiotherapists. The primary outcome is the post-exercise FEV1 decline percentage. Secondary outcomes include inspiratory and expiratory muscle strength, exercise tolerance measured by VO2 Max, and health-related quality of life using the SF-36 questionnaire. Assessments will be conducted at baseline and after 5 weeks of intervention. The study aims to provide evidence for non-pharmacological management of Exercise-Induced Bronchospasm in competitive athletes, offering an alternative approach that aligns with anti-doping regulations and holistic training preferences. This research addresses a significant gap in respiratory rehabilitation applications for athletes with exercise-induced airway narrowing and may inform clinical guidelines for this population.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Masking
- Investigator Blinded
Eligibility Criteria
- Ages
- 18.00 Year(s) to 45.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Age 18–45 years.
- •On screening, confirmed EIB FEV 1 decline of more than 10 percent Actively training long-distance runners more than 40 km per week No chronic respiratory conditions Willing to complete 5 week intervention and assessments.
Exclusion Criteria
- •Recent respiratory infection (more than 4 weeks).
- •Significant comorbidities (e.g., cardiovascular disease, diabetes mellitus asthma ).
- •Participation in conflicting clinical trials.
- •Pregnancy or lactation.
Outcomes
Primary Outcomes
decline percentage of forced expiratory volume for 1 second
Time Frame: decline percentage of forced expiratory volume for 1 second
Secondary Outcomes
- IMP(EMP)
Investigators
vishagh kumar v nair
Bharati Vidyapeeth (DU) School of Physiotherapy, Sangli