Inspiratory Muscle Training Enhances Jumping Power and Shoot-ing Performance in Elite Air Pistol Athletes

February 6, 2026 updated by: Coşkun YILMAZ, Gümüşhane Universıty
This randomized controlled trial investigated the effects of a four-week inspiratory muscle training (IMT) program on physical and motor performance parameters and shooting accuracy in elite male air pistol athletes. Twenty athletes were randomly assigned to either an IMT group or a control group. Outcome measures included jumping performance, reaction time, flexibility, and shooting accuracy assessed via the SCATT system. The findings demonstrated that IMT significantly improved lower-limb explosive power and shooting performance without affecting reaction time or flexibility.

Study Overview

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

Interventional

Enrollment (Actual)

20

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Trabzon, Ordu, Giresun, Rize, Artvin, Gümüşhane
      • Gümüşhane, Trabzon, Ordu, Giresun, Rize, Artvin, Gümüşhane, Turkey (Türkiye), 29600
        • Gumushane Univetsity

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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.
No Intervention: Control Group
Participants continued their regular air pistol training routines without inspiratory muscle training.

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
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
Squat Jump Height and Power
Time Frame: 4 Weeks
Measured using OptoJump Next system
4 Weeks
Visual Reaction Time
Time Frame: 4 weeks
Assessed using Cognitech reaction time tester
4 weeks
Auditory Reaction Time
Time Frame: 4 week
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

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 5, 2025

Primary Completion (Actual)

October 15, 2025

Study Completion (Actual)

October 20, 2025

Study Registration Dates

First Submitted

February 6, 2026

First Submitted That Met QC Criteria

February 6, 2026

First Posted (Actual)

February 12, 2026

Study Record Updates

Last Update Posted (Actual)

February 12, 2026

Last Update Submitted That Met QC Criteria

February 6, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

The individual participant data collected in this study will not be shared with other researchers due to the need to protect participant confidentiality and the lack of permission for data sharing within the scope of informed consent.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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