- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07406451
Inspiratory Muscle Training Enhances Jumping Power and Shoot-ing Performance in Elite Air Pistol Athletes
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Air pistol shooting is a precision sport requiring postural stability, neuromuscular coordination, and controlled breathing. Inspiratory muscle training has been shown to enhance respiratory muscle strength, trunk stability, and neuromuscular efficiency. However, evidence regarding its effects in precision sports is limited.
This study employed a four-week parallel-group randomized controlled design to examine whether IMT improves jumping performance, reaction time, and shooting accuracy in elite air pistol athletes. The IMT group performed twice-daily resisted breathing sessions using a POWERbreathe® device, while the control group continued standard training. Performance outcomes were assessed before and after the intervention period.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Trabzon, Ordu, Giresun, Rize, Artvin, Gümüşhane
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Gümüşhane, Trabzon, Ordu, Giresun, Rize, Artvin, Gümüşhane, Turkey (Türkiye), 29600
- Gumushane Univetsity
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Male athletes aged 18-35 years
- Minimum of 3 years of systematic air pistol shooting experience
- Regular training for at least the previous 6 months
- Medically cleared for physical activity
Exclusion Criteria:
- History of respiratory, cardiovascular, neurological, or musculoskeletal disorders
- Current injury affecting performance
- Participation in respiratory muscle training within the last 6 months
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: Inspiratory Muscle Training (IMT) Group
Participants performed inspiratory muscle training using a POWERbreathe® Classic device.
Training consisted of two daily sessions of 30 resisted breaths, six days per week, for four weeks.
Initial resistance was set at 40% of maximal inspiratory pressure (MIP) and progressively increased weekly.
|
Participants performed inspiratory muscle training using a POWERbreathe® Classic device.
Training consisted of two daily sessions of 30 resisted breaths, six days per week, for four weeks.
Initial resistance was set at 40% of maximal inspiratory pressure (MIP) and progressively increased weekly.
Participants continued their regular air pistol training routines without inspiratory muscle training.
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No Intervention: Control Group
Participants continued their regular air pistol training routines without inspiratory muscle training.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Shooting Performance (SCATT Score)
Time Frame: 4 weeks
|
Shooting accuracy and stability assessed using the SCATT shooting simulation system
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4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Countermovement Jump Height and Power
Time Frame: 4 Weeks
|
Measured using OptoJump Next system
|
4 Weeks
|
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Squat Jump Height and Power
Time Frame: 4 Weeks
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Measured using OptoJump Next system
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4 Weeks
|
|
Visual Reaction Time
Time Frame: 4 weeks
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Assessed using Cognitech reaction time tester
|
4 weeks
|
|
Auditory Reaction Time
Time Frame: 4 week
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Assessed using Cognitech reaction time tester
|
4 week
|
|
Flexibility (Sit-and-Reach Test)
Time Frame: 4 week
|
Flexibility (Sit-and-Reach Test)
|
4 week
|
Collaborators and Investigators
Sponsor
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2025-019
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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