High vs Low Volume Intensity Training With IMT On Pulmonary Function And Breathing Efficiency On Recreational Swimmers.
Comparison of High Volume Intensity Training and Low Volume Intensity Training With IMT on Pulmonary Function and Breathing Efficiency of Recreational Swimmers
1 other identifier
interventional
64
1 country
1
Brief Summary
This study aims to evaluate the impact of inspiratory muscle training (IMT) on respiratory function and swimming performance in competitive swimmers. Given the importance of optimal respiratory function in swimming, this trial investigates whether IMT can improve swimming performance metrics, such as lap times and endurance, and overall respiratory health.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started May 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 18, 2024
CompletedFirst Posted
Study publicly available on registry
September 19, 2024
CompletedStudy Start
First participant enrolled
May 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2025
CompletedAugust 19, 2025
August 1, 2025
2 months
September 18, 2024
August 18, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Peak Expiratory Flow Rate (PEFR)
Peak expiratory flow rate (PEFR) Peak expiratory flow rate (PEFR) measured through digital spirometer. Peak Expiratory Flow Rate (PEFR) measured through digital spirometer. Three zones of measurement are commonly used to interpret peak flow rates. Normal value of PEFR is (80-100%). Green zone indicates 80 to 100 percent of the usual or normal peak flow reading, yellow zone indicates 50 to 79 percent of the usual or normal peak flow readings, and red zone indicates less than 50 percent of the usual or normal peak flow readings.
6 weeks
Forced Vital Capacity (FVC)
Forced vital capacity (FVC) measured through digital spirometer. If the value of FVC is within 80% of the reference value, the results are considered normal. Changes in FVC from baseline to 3rd week and after 6 weeks day of intervention will be assessed.
6 weeks
Forced Expiratory volume in 1sec (FEV1)
Forced expiratory volume in 1sec (FEV1) measured through digital spirometer. If the value of FEV1 is within 80% of the reference value, the results are considered normal.
6 weeks
Swimming efficiency (SWOLF) score
A SWOLF score is a metric used in swimming to assess efficiency. It combines the time it takes to swim a distance (in seconds) with the number of strokes taken to complete that distance.
6 weeks
Study Arms (2)
High volume intensity (HVIMT)
EXPERIMENTALHigh-volume intensity inspiratory muscle training (IMT) is a therapeutic approach designed to improve respiratory muscle strength and endurance. In this clinical trial, participants will engage in a structured regimen of inspiratory exercises with high resistance and significant repetition volume. Participants will perform inspiratory muscle exercises using power breath that provides high resistance, with a focus on both intensity and volume. The protocol involves 3 sessions per day for 6 weeks.
Low volume intensity LVIMT
EXPERIMENTALParticipants will engage in a structured training program involving inspiratory muscle exercises with high resistance and a high volume of repetitions. The regimen includes multiple sessions per day over several weeks, using specialized inspiratory muscle training devices. Changes in inspiratory muscle strength (measured by maximal inspiratory pressure) and endurance.
Interventions
IMT is a form of exercise designed to strengthen the muscle involved inhalation, primarily the diaphragm and intercostal muscles. The LVIMT group will perform IMT once daily, 5 days a week, maintaining 60% of maximal inspiratory pressure (MIP) throughout the 6-week intervention. The intervals are typically longer in duration (e.g., 2-4 minutes) with a work-to-rest ratio of 1:1 or 1:0.5. POSITION: rested and seated position. FREQUENCY: more frequency, once a day. 2-3 sessions per week. INTENSITY: Low resistance. Only 60%% MIP. TIME: shorter duration of 10-20 mint.
The HVIMT group is trained twice daily, with the morning session matching the LV-IMT protocol, and an additional afternoon session. The HVIMT group also experienced a progressive increase in intensity, starting at 60% MIP and reaching 80% by the end of the study. LVIMT works for beginner or individuals with limited respiratory capacity while HVIMT is used for individual with high baseline respiratory fitness. The intervals are typically shorter in duration (e.g., 30 seconds to 2 minutes) with a work-to-rest ratio of 1:1 or 1:2. POSITION; Seated upright position. FREQUENCY: more frequency two session per week. 4-5 sessions per week. INTENSITY: high resistance. 60%-80% MIP. (gradual increment the load by 10% every 2 weeks to reach 80% MIP) TIME: longer duration 20-30 mint.
Eligibility Criteria
You may qualify if:
- Male and Female Swimmers
- Age; 18-25
- Minimum of 2 years of regular swimming training experience, with at least 3 swimming sessions per week.
You may not qualify if:
- Refusal to participate in the study.
- History of respiratory or cardiovascular conditions that could impact participation or results.
- Participation in any other respiratory or exercise-related intervention study within the last 6 months.
- Consumption of any medications or supplements that could potentially influence respiratory or cardiovascular function.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Bahira Active Club.
Islamabad, Federal, 04403, Pakistan
Study Officials
- PRINCIPAL INVESTIGATOR
Suman Sheraz, PhD
Riphah International University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 18, 2024
First Posted
September 19, 2024
Study Start
May 1, 2025
Primary Completion
June 30, 2025
Study Completion
June 30, 2025
Last Updated
August 19, 2025
Record last verified: 2025-08
Data Sharing
- IPD Sharing
- Will not share