ClinicalTrials.gg
CompletedNCT07887282Updated Oct 21, 2026

The Effects of Interval Respiratory Muscle Training on Athletic Performance

An interventional study of IMT %40 MIP and IMT %50-60-70-80 in Respiratory Muscle Training, Inspiratory Muscle Strength and Maximal Oxygen Consumption, sponsored by Ondokuz Mayıs University. Completed at 1 site in Turkey (Türkiye). Open to male participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-21.

Sponsored by Ondokuz Mayıs University · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Registered 1 year 3 months after the study started (first participant enrolled Sep 2024, registered Jan 2026).
Updated Oct 21, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
23
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
Male
01

Study summary

This study evaluated the effects of a 4-week respiratory muscle training (RMT) program using constant versus incremental threshold resistance on respiratory muscle strength, pulmonary function, extremity strength, and aerobic/anaerobic endurance in trained athletes. Participants were randomized into two groups: the Constant IMT group (trained at a fixed 40% of maximal inspiratory pressure [MIP]) and the Incremental IMT group (progressing weekly from 50% to 80% of MIP). Both groups trained twice daily, 5 days per week (2 sets of 30 breaths/day) for 4 weeks. Standardized physiological, spirometric, and athletic performance tests were assessed at baseline and post-intervention.

Read the detailed description

The purpose of this randomized, controlled trial was to compare the physiological and athletic performance adaptations induced by constant versus progressive-load inspiratory muscle training (IMT) in competitive athletes.

Inspiratory muscle fatigue can trigger the respiratory metaboreflex, causing sympathetic vasoconstriction in locomotor muscles and compromising exercise tolerance. Strengthening the inspiratory muscles is hypothesized to attenuate this reflex and improve limb muscular endurance and aerobic capacity.

Participants completed a 4-week intervention with a threshold inspiratory device (PowerBreathe).

  • Constant IMT Group: Performed 2 daily sessions (morning and evening) of 30 breaths at a fixed intensity of 40% MIP, 5 days per week.
  • Incremental IMT Group: Performed 2 daily sessions of 30 breaths, 5 days per week, starting at 50% MIP in Week 1, and progressing weekly to 60%, 70%, and 80% MIP in Weeks 2, 3, and 4, respectively.

Initial sessions were supervised in the exercise physiology laboratory, with remaining sessions performed under remote video monitoring. Outcomes were evaluated across multiple laboratory visits before and 48 hours following the 4-week protocol.

02

Conditions studied

  • Respiratory Muscle Training
  • Inspiratory Muscle Strength
  • Maximal Oxygen Consumption

Keywords

  • Respiratory Muscle Training
  • Functional Performance
  • Strength
  • MaxVO₂
  • Athlete
03

In context

Lead sponsor

Ondokuz Mayıs University is the lead sponsor of 275 studies on the registry; 68 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Between the ages of 18 and 30,
  • Having at least 5 years of active training experience,
  • Having a regular training frequency of at least 4 days per week

Exclusion criteria

Exclusion Criteria:

  • Having a history of lung dysfunction and cardiovascular disease,
  • Having had a lower or upper respiratory tract infection within the last four weeks,
  • Having a history of smoking,
  • Having any ongoing disability
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
23 participants (actual)

Study arms

  • Experimental
    Constant IMT Group

    Athletes performed fixed-resistance inspiratory muscle training using a PowerBreathe threshold device twice daily, 5 days per week for 4 weeks (2 sets of 30 repetitions/day) maintained at a constant 40% MIP throughout the intervention.

    Device: IMT %40 MIP

  • Experimental
    Incremental IMT Group

    Athletes performed progressive inspiratory muscle training using a PowerBreathe threshold device twice daily, 5 days per week for 4 weeks (2 sets of 30 repetitions/day). Resistance started at 50% MIP and increased weekly by 10% (50%, 60%, 70%, and 80% MIP).

    Device: IMT %50-60-70-80

Interventions

  • DeviceIMT %40 MIP

    This study examined two inspiratory muscle training (IMT) protocols using the PowerBreathe device. Participants in both groups performed IMT twice daily, five days a week, for four weeks. Each session included 30 inspiratory breaths, totaling 60 breaths per day. The Constant IMT group trained with a fixed resistance of 40% MIP throughout the intervention. All participants received supervised instruction during the initial session. Subsequent sessions were home-based, monitored weekly through video submissions and participant check-ins. This design enables a structured comparison between progressive and constant loading in IMT for improving respiratory strength and endurance in trained athletes.

    Also known as: The Constant IMT group trained with a fixed resistance of 40% MIP throughout the intervention.

  • DeviceIMT %50-60-70-80

    This study examined two inspiratory muscle training (IMT) protocols using the PowerBreathe device. Participants in both groups performed IMT twice daily, five days a week, for four weeks. Each session included 30 inspiratory breaths, totaling 60 breaths per day. The Incremental IMT group began training at 50% of Maximal Inspiratory Pressure (MIP), with resistance increased weekly to 60%, 70%, and 80%. All participants received supervised instruction during the initial session. Subsequent sessions were home-based, monitored weekly through video submissions and participant check-ins. This design enables a structured comparison between progressive and constant loading in IMT for improving respiratory strength and endurance in trained athletes.

    Also known as: The Incremental IMT group began training at 50% of Maximal Inspiratory Pressure (MIP), with resistance increased weekly to 60%, 70%, and 80%.

06

What researchers measure

Primary outcomes

  1. Change in maximal inspiratory pressure (MIP)

    Maximal inspiratory pressure (MIP) will be measured using a device with a respiratory pressure measurement function and expressed in cmH2O. Change will be calculated as the Week 4 value minus the baseline value.

    Time frame: Baseline and Week 4 (end of the intervention).

  2. Change in Maximal Expiratory Pressure (MEP)

    Maximal expiratory pressure was measured from total lung capacity against an occluded airway using a digital respiratory pressure meter (MicroRPM) and expressed in cmH2O. Change was calculated as Week 4 minus baseline.

    Time frame: Baseline and Week 4 (end of the intervention).

Secondary outcomes

  1. Change in forced vital capacity (FVC)

    Forced vital capacity (FVC) will be measured by spirometry and expressed in liters. Change will be calculated as the Week 4 value minus the baseline value.

    Time frame: Baseline and Week 4 (end of the intervention).

  2. Change in Forced Expiratory Volume in 1 Second (FEV1)

    Volume exhaled in the first second of a forced exhalation maneuver was measured using spirometry, expressed in liters (L).

    Time frame: Baseline and Week 4 (end of the intervention).

  3. Change in FEV1/FVC Ratio

    The ratio of forced expiratory volume in 1 second to forced vital capacity was assessed using spirometry, expressed as a percentage (%).

    Time frame: Baseline and Week 4 (end of the intervention).

  4. Change in Slow Vital Capacity (SVC)

    Vital capacity measured during relaxed, unforced breathing using spirometry, expressed in liters (L).

    Time frame: Baseline and Week 4 (end of the intervention).

  5. Change in Maximal Voluntary Ventilation (MVV)

    Maximal volume of air ventilated over a 12-second sprint breathing protocol was extrapolated to liters per minute (L/min).

    Time frame: Baseline and Week 4 (end of the intervention).

  6. Change in Seated Medicine Ball Throw Distance

    Upper body explosive power was measured by throwing a 3 kg medicine ball overhead from a seated position with the back supported against a wall. The maximum distance achieved across three trials was recorded in centimeters (cm).

    Time frame: Baseline and Week 4 (end of the intervention).

  7. Change in 30-Second Modified Push-Up Repetitions

    Upper body muscular endurance was evaluated by counting the maximum number of correctly executed push-up repetitions performed within 30 seconds.

    Time frame: Baseline and Week 4 (end of the intervention).

  8. Change in 1-Minute Sit-Up Repetitions

    Abdominal muscular endurance was evaluated by recording the maximum number of correctly executed sit-up repetitions completed in 60 seconds.

    Time frame: Baseline and Week 4 (end of the intervention).

  9. Change in 1-Repetition Maximum (1RM) Bench Press Strength

    Maximal upper body dynamic strength was assessed via 1RM barbell bench press test protocol, expressed in kilograms (kg).

    Time frame: Baseline and Week 4 (end of the intervention).

  10. Change in 1-Repetition Maximum (1RM) Back Squat Strength

    Maximal lower body dynamic strength was determined using a standard 1RM barbell back squat protocol, expressed in kilograms (kg).

    Time frame: Baseline and Week 4 (end of the intervention).

  11. Change in Isometric Hand Grip Strength

    Isometric hand grip strength was assessed using a Takei hand dynamometer for dominant and non-dominant hands, recorded in kilograms (kg).

    Time frame: Baseline and Week 4 (end of the intervention).

  12. Change in Isometric Back and Leg Strength

    Isometric back and leg strength were evaluated using a Takei digital back-and-leg dynamometer, recorded in kilograms (kg).

    Time frame: Baseline and Week 4 (end of the intervention).

  13. Change in Vertical Jump Height

    Explosive lower extremity power was evaluated via vertical jump test using a jump meter (KK 5406 Jumpmeter). The best attempt was recorded in centimeters (cm).

    Time frame: Baseline and Week 4 (end of the intervention).

  14. Change in Single Leg Hop Performance and Limb Symmetry Index

    Functional lower extremity performance was measured using single-leg hop test protocols (single hop, triple hop, crossover hop, and side hop). Maximum distance was recorded in cm, and the Limb Symmetry Index (LSI, %) was calculated.

    Time frame: Baseline and Week 4 (end of the intervention).

  15. Change in Anaerobic Peak and Mean Power (Wingate Test)

    Anaerobic power was evaluated using a 30-second all-out Wingate test on a Monark 894E cycle ergometer against a resistance of 7.5% body weight, expressed in Watts (W).

    Time frame: Baseline and Week 4 (end of the intervention).

  16. Change in Estimated Maximal Oxygen Consumption (VO2max)

    Aerobic capacity was evaluated using the Bruce Treadmill Test protocol. The test began on a motorized treadmill at 2.74 km/h and a 10% incline, with speed and incline increasing every 3 minutes until volitional exhaustion. Total test duration (T, in minutes) was recorded, and VO2max was estimated using the standardized regression equation: VO2max = 14.8 - (1.379 \* T) + (0.451 \* T\^2) - (0.012 \* T\^3), expressed in mL/kg/min. Change was calculated as Week 4 minus baseline.

    Time frame: Baseline and Week 4 (end of the intervention) .

07

Study locations

1 site
  • Faculty of Sport Science
    Kahramanmaraş, Onikişubat 46050, Turkey (Türkiye)
08

References and documents

Publications

  • Gomes Neto M, Ferrari F, Helal L, Lopes AA, Carvalho VO, Stein R. The impact of high-intensity inspiratory muscle training on exercise capacity and inspiratory muscle strength in heart failure with reduced ejection fraction: a systematic review and meta-analysis. Clin Rehabil. 2018 Nov;32(11):1482-1492. doi: 10.1177/0269215518784345. Epub 2018 Jul 9. PubMed 29984598 ↗
  • Gething AD, Williams M, Davies B. Inspiratory resistive loading improves cycling capacity: a placebo controlled trial. Br J Sports Med. 2004 Dec;38(6):730-6. doi: 10.1136/bjsm.2003.007518. PubMed 15562168 ↗
  • Fernandez-Lazaro D, Gallego-Gallego D, Corchete LA, Fernandez Zoppino D, Gonzalez-Bernal JJ, Garcia Gomez B, Mielgo-Ayuso J. Inspiratory Muscle Training Program Using the PowerBreath(R): Does It Have Ergogenic Potential for Respiratory and/or Athletic Performance? A Systematic Review with Meta-Analysis. Int J Environ Res Public Health. 2021 Jun 22;18(13):6703. doi: 10.3390/ijerph18136703. PubMed 34206354 ↗
  • Cunha M, Mendes F, Paciencia I, Rodolfo A, Carneiro-Leao L, Rama T, Rufo J, Delgado L, Moreira A. The effect of inspiratory muscle training on swimming performance, inspiratory muscle strength, lung function, and perceived breathlessness in elite swimmers: a randomized controlled trial. Porto Biomed J. 2019 Oct 24;4(6):e49. doi: 10.1097/j.pbj.0000000000000049. eCollection 2019 Nov-Dec. PubMed 33501396 ↗
  • Charususin N, Dacha S, Gosselink R, Decramer M, Von Leupoldt A, Reijnders T, Louvaris Z, Langer D. Respiratory muscle function and exercise limitation in patients with chronic obstructive pulmonary disease: a review. Expert Rev Respir Med. 2018 Jan;12(1):67-79. doi: 10.1080/17476348.2018.1398084. Epub 2017 Nov 6. PubMed 29072087 ↗
  • Chang YC, Chang HY, Ho CC, Lee PF, Chou YC, Tsai MW, Chou LW. Effects of 4-Week Inspiratory Muscle Training on Sport Performance in College 800-Meter Track Runners. Medicina (Kaunas). 2021 Jan 15;57(1):72. doi: 10.3390/medicina57010072. PubMed 33467421 ↗
  • Piskin NE, Aktug ZB, Kara M, Yavuz G, Ozturk GT, Ibis S, Aka H. The Effect of Blood Flow Restriction Training on Isokinetic Strength Muscle Thickness and Athletic Performance. J Musculoskelet Neuronal Interact. 2025 Jun 1;25(2):208-218. doi: 10.22540/JMNI-25-208. PubMed 40452197 ↗
  • Bostanci O, Mayda H, Yilmaz C, Kabadayi M, Yilmaz AK, Ozdal M. Inspiratory muscle training improves pulmonary functions and respiratory muscle strength in healthy male smokers. Respir Physiol Neurobiol. 2019 Jun;264:28-32. doi: 10.1016/j.resp.2019.04.001. Epub 2019 Apr 3. PubMed 30953791 ↗

Study documents

  • Protocol and informed consent form · Jul 31, 2024
  • Informed consent form · Jul 31, 2024

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Sep 2024 to primary completion in Nov 2024, 1 month.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 2, 2026
First posted
Oct 21, 2026
StartActual
Sep 15, 2024
Primary completionActual
Nov 10, 2024
CompletionActual
Nov 11, 2024
Last update
Oct 21, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 21, 2026
Show all 1 update
  1. Oct 21, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07887282
Responsible party
Ali Kerim Yılmaz (associate professor, Ondokuz Mayıs University) — Principal investigator
First posted
Oct 21, 2026
Start date
Sep 15, 2024
Primary completion
Nov 10, 2024
Completion
Nov 11, 2024
Last update
Oct 21, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion