- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06604741
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
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Federal
-
Islamabad, Federal, Pakistan, 04403
- Bahira Active Club.
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Male and Female Swimmers
- Age; 18-25
- Minimum of 2 years of regular swimming training experience, with at least 3 swimming sessions per week.
Exclusion Criteria:
- 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.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: High volume intensity (HVIMT)
High-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. |
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. |
|
Experimental: Low volume intensity LVIMT
Participants 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. |
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. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Peak Expiratory Flow Rate (PEFR)
Time Frame: 6 weeks
|
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)
Time Frame: 6 weeks
|
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)
Time Frame: 6 weeks
|
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
Time Frame: 6 weeks
|
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
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Suman Sheraz, PhD, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Sumayya Karim
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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