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Acute Effects of Inspiratory Muscle Warm-up on Muscular Performance and Pulmonary Function in Natural Bodybuilders

Acute Effects of Inspiratory Muscle Warm-up on Muscular Performance and Pulmonary Function in Natural Bodybuilders

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07390149
Acronym
IWU and 1RM
Enrollment
27
Registered
2026-02-05
Start date
2025-01-05
Completion date
2026-01-05
Last updated
2026-05-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Exercise Physiology, Sports Performance

Keywords

acute interventions, human physiology, inspiratory muscle warm-up, exercise performance, bodybuilders, 1RM

Brief summary

The present study aims to investigate the acute effects of inspiratory muscle warm-up (IWU) on 1RM performance in professional natural bodybuilders. The hypothesis is that IWU will lead to an increase in the pressure-generating capacity of the inspiratory muscles, thereby resulting in improved 1RM strength performance. The anticipated findings are expected to contribute not only to the enhancement of maximal strength performance but also to the improvement of exercise efficiency through increased respiratory muscle endurance. It is submitted that these outcomes may ultimately provide insights into the long-term sustainability of professional athletes' performance. Twenty male athletes who had competed in national and international professional natural bodybuilding competitions were recruited for this study. The participants had an average experience in natural bodybuilding of 3.21 years, with a standard deviation of ± 1.44 years, and trained for more than five hours per week. The data collection period commenced in July 2025. The study was designed as a randomized controlled experimental trial. Participants were randomly assigned to two groups by a computerized program at three visits after the trial, based on their first measurement: inspiratory warm-up (IWU) group or control (CON) group.

Detailed description

The data collection period occurred between the 1st and 6th of July 2025. Prior to their involvement in the study, all subjects provided both verbal and written informed consent. Participants were invited to visit the laboratory on three separate occasions. During the preliminary visit, the subjects underwent a series of pulmonary function tests (PFTs). These included measurements of maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP). The participants were also subjected to 1RM testing and three practice trials of both the inspiratory warm-up and general training warm-up procedures \[14\]. On the second occasion, the PFT and MIP-MEP tests were conducted without any warm-up protocols, followed by the assessment of 1RM performance. On the third occasion, the participants were divided into two groups: the experimental group (IWU), which performed both inspiratory muscle and general warm-up exercises, and the control group (CON), which performed only the general warm-up. Each group comprised ten professional male natural bodybuilders. PFT and MIP-MEP tests were reassessed, and 1RM performance was measured immediately following the IWU intervention. In order to control for circadian variations, all laboratory visits were conducted at the same time of day (between 09:00 and 12:00). Participants were notified 72 hours in advance of each visit and were instructed to refrain from high-intensity physical activity during that period. It was determined that a recovery period of 72 hours should be observed between each testing session.

Interventions

OTHERIWU

The IWU group performed both inspiratory muscle warm-up and standard exercise warm-up.

OTHERControl

The CON group performed only the standard warm-up.

Sponsors

Gümüşhane Universıty
Lead SponsorOTHER
Çankırı Karatekin University
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
NONE

Intervention model description

This study used a randomized, parallel-group design. Participants were randomly allocated to either the inspiratory warm-up (IWU) group or the control (CON) group. All participants completed baseline assessments prior to randomization and remained in their assigned group throughout the study. No crossover between conditions was implemented. Outcome measures were assessed across multiple visits to evaluate pre- and post-intervention responses within each group.

Eligibility

Sex/Gender
MALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* They were professional natural bodybuilders with less than three years of experience. , * Male professional natural bodybuilders aged 18-35 years --Full participation in training and matches during the previous 6 months, * Ability to perform maximal exercise testing

Exclusion criteria

* Individuals were deemed ineligible on the basis of a medical history that included any chronic or acute respiratory disease. * Individuals were considered ineligible if they were taking any prescription medication that could affect their response to exercise. * In accordance with the stipulated criteria, individuals were deemed to be ineligible for participation in the study if they had a history of current smoking or had smoked within the past year. * Individuals were considered ineligible for participation in the study if they had participated in similar studies within the previous six months. * Prior to participation, all individuals were required to sign a formal waiver, thereby affirming their adherence to the World Anti-Doping Agency Code.

Design outcomes

Primary

MeasureTime frameDescription
1RMDay 1One-Repetition maximum (1RM) bench press performance
maximal inspiratory pressures (MIP )Day 1maximal inspiratory pressures (MIP )

Secondary

MeasureTime frameDescription
maximal expiratory pressures (MEP)Day 1maximal expiratory pressures (MEP)
Forced vital capacity (FVC)Day 1Pulmonary function parameter, including forced vital capacity (FVC), the total volume of air exhaled forcefully after a maximal deep inhalation, were measured using a MGF Diagnostics CPFS/D USB spirometer
forced expiratory volume in one second (FEV1)Day 1Pulmonary function parameter, including forced vital capacity (FEV1), the total volume of air exhaled forcefully after a maximal deep inhalation, were measured using a MGF Diagnostics CPFS/D USB spirometer
FEV1/FVC ratio (Tiffeneau index)Day 1Pulmonary function parameter, including forced vital capacity (FEV1/FVC), the total volume of air exhaled forcefully after a maximal deep inhalation, were measured using a MGF Diagnostics CPFS/D USB spirometer
peak expiratory flow (PEF)Day 1Pulmonary function parameter, including forced vital capacity (FVC), the total volume of air exhaled forcefully after a maximal deep inhalation, were measured using a MGF Diagnostics CPFS/D USB spirometer

Countries

Turkey (Türkiye)

Contacts

STUDY_CHAIRCoşkun YILMAZ, associate professor

Gümüşhane Üniversity

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 2, 2026