The Effect of Inspiratory Muscle Training on Respiratory Parameters, Balance, Trunk Endurance and Trunk Isokinetic Muscle Strength in Wrestling Athletes
NCT ID: NCT07083258
Last Updated: 2025-11-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
NA
30 participants
INTERVENTIONAL
2025-12-15
2026-12-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The Effects of Inspiratory Muscle Training on Respiratory Parameters, Balance, Trunk Endurance, and Trunk Isokinetic Muscle Strength in Elite Female Freestyle Wrestlers
Objective:
This experimental study aims to investigate the effects of inspiratory muscle training on respiratory functions, trunk muscle strength, endurance, and balance in elite female freestyle wrestlers.
Methods:
This randomized controlled trial will include 30 elite female freestyle wrestlers aged between 16 and 22. Participants will be randomly assigned to either an intervention group or a placebo control group using a simple randomization method. The intervention group will receive progressive inspiratory muscle training with the POWERbreathe Plus device, 5 days per week for 4 weeks. The training load will increase weekly. The control group will undergo low-resistance inspiratory training set at 15% of their baseline maximal inspiratory pressure (MIP), serving as a placebo. Pre- and post-intervention assessments will be conducted by a blinded evaluator.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Investigation of Inspiratory Muscle Training Applied at Different Intensities on Intercostal Muscle Oxygenation
NCT07029074
Effects of Wrestling Training on Psychological Well-Being, Anxiety, and Resilience in Adolescent Sedanter Boys
NCT07193121
Effects of Inspiratory Muscle Training on Diaphragm Thickness, Respiratory Muscle Strength and Balance in Dancers.
NCT04845802
Inspiratory Muscle Training and Expiratory Muscle Thickness
NCT06251791
Inspiratory Muscle Training After Vertebroplasty in Osteoporotic Fracture Patients
NCT07024095
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Scientific Background and Rationale Freestyle wrestling is a physically demanding sport that requires simultaneous, dynamic use of both upper and lower extremities, along with high levels of strength, balance, and coordination. Success in competition is closely linked to factors such as postural stability, core muscle activation, and the ability to generate isometric and dynamic force. However, the contribution of respiratory muscles to athletic performance has often been overlooked or assessed only indirectly in previous studies.
Given the high-intensity and short-duration nature of wrestling matches, increased ventilatory demand places a significant burden on the diaphragm and accessory respiratory muscles. Recent evidence suggests that IMT not only improves pulmonary function but also enhances core stabilization and postural control. Therefore, directly assessing the effects of IMT on respiratory and trunk muscle performance in elite female wrestlers addresses a notable gap in the literature.
Study Design This is a randomized controlled experimental study involving 30 elite female freestyle wrestlers affiliated with the Turkish Olympic Preparation Center (TOHM-Trabzon). Participants will be randomly assigned into two groups (n=15 each) via simple randomization.
The intervention group will undergo IMT using the POWERbreathe Plus device, 5 days per week for 4 weeks. Training will begin at 50% of the participants' MIP and increase by 10% each week, reaching 80% by the final week.
The control group will receive placebo IMT at a constant load equivalent to 15% of baseline MIP, following the same training schedule.
All interventions will be delivered in addition to the athletes' regular training programs. Pre- and post-intervention assessments will be conducted by a blinded physiotherapist who is not involved in the implementation of the training.
Assessment Parameters and Instruments To comprehensively evaluate the impact of IMT, objective and validated tools will be employed. Pulmonary function will be assessed using the Cosmed Pony FX device, measuring MIP, MEP, FEV1, FVC, and the FEV1/FVC ratio. Trunk endurance will be evaluated using the McGill Core Endurance protocol, which includes tests for trunk flexion, extension, and lateral plank. Muscle strength will be measured using the Isomed 2000 isokinetic dynamometer at a velocity of 60°/s to determine peak torque during trunk flexion and extension. Balance performance will be assessed with both the Y Balance Test (in anterior, posterolateral, and posteromedial directions) and the Flamingo Balance Test, which measures the ability to maintain single-leg stance. In addition, a participant tracking form will be used to record demographic information, training history, and attendance. All assessments will be performed under standardized conditions by a blinded evaluator.
Statistical Methods Appropriate statistical methods will be employed to analyze the data. Distribution characteristics and group comparisons will be assessed accordingly. Intra-group and inter-group differences, as well as time-by-group interactions, will be analyzed. Effect sizes will be calculated using standard procedures, and statistical significance will be set at p \< 0.05.
Original Contribution of the Study This study is unique in its comprehensive evaluation of the effects of IMT not only on performance-related physical parameters but also on cardiopulmonary capacity in elite athletes. By focusing specifically on female wrestlers, the study contributes to sex-specific physiological research and is expected to provide evidence for the development of clinically applicable IMT protocols aimed at enhancing athletic performance and health.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Inspiratory Muscle Training Program
Participants in this group will receive a progressive inspiratory muscle training (IMT) program using the POWERbreathe Plus device. Training will be conducted 5 days per week for 4 weeks. The intensity will start at 50% of the participant's measured maximal inspiratory pressure (MIP) and will be increased by 10% each week, reaching 80% in the final week. All training will be performed in addition to the athletes' regular wrestling sessions. Participants in this group will be assessed for respiratory parameters, trunk endurance, balance, and trunk isokinetic muscle strength before and after the intervention.
Progressive Inspiratory Muscle Training (IMT)
The intervention involves the application of inspiratory muscle training using the POWERbreathe Plus device. Training will be conducted at an initial intensity of 50% of the individual's MIP and will be increased weekly by 10%, reaching 80% by week four. Sessions will take place 5 days per week and consist of 2 sets of 30 repetitions per day, with 2-minute rest intervals between sets. This training aims to improve inspiratory muscle strength and endurance, as well as core stability, respiratory function, dynamic balance, and trunk isokinetic strength.
Control Group
Participants in the control group will receive a sham inspiratory muscle training program using the same device. The training intensity will be fixed at 15% of the initial MIP throughout the 4-week period to produce a placebo effect. The frequency and duration of training will mirror that of the experimental group. Participants will undergo identical pre- and post-intervention evaluations.
Placebo Training
The placebo group will perform identical training sessions using the same device but with a constant minimal resistance set at 15% of the initial MIP, insufficient to induce a physiological training effect. This intervention is designed to control for placebo response. Assessment protocols will be identical to those in the experimental group.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Progressive Inspiratory Muscle Training (IMT)
The intervention involves the application of inspiratory muscle training using the POWERbreathe Plus device. Training will be conducted at an initial intensity of 50% of the individual's MIP and will be increased weekly by 10%, reaching 80% by week four. Sessions will take place 5 days per week and consist of 2 sets of 30 repetitions per day, with 2-minute rest intervals between sets. This training aims to improve inspiratory muscle strength and endurance, as well as core stability, respiratory function, dynamic balance, and trunk isokinetic strength.
Placebo Training
The placebo group will perform identical training sessions using the same device but with a constant minimal resistance set at 15% of the initial MIP, insufficient to induce a physiological training effect. This intervention is designed to control for placebo response. Assessment protocols will be identical to those in the experimental group.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Participating in regular training at least 4 days a week.
3. To volunteer to participate in the study.
4. Being an athlete within TOHM for at least one year.
5. To be between the ages of 16-22.
Exclusion Criteria
2. Have specific balance problems (e.g., vestibular or neurological impairment).
16 Years
22 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ondokuz Mayıs University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
MİNE PEKESEN KURTÇA
Ass.Prof.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Ondokuz Mayıs Üniversitesi
Samsun, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
OMÜ2025/257
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.