このページは自動翻訳されたものであり、翻訳の正確性は保証されていません。を参照してください。 英語版 ソーステキスト用。

Effects of Diaphragmatic Breathing Retraining in Combat Sport Athletes With Dysfunctional Breathing Patterns

2026年7月15日 更新者:YI-JU TSAI、National Cheng Kung University

Dysfunctional Breathing Patterns, Diaphragmatic Function, Core Stability, and Postural Control in Combat Sport Athletes: Diaphragm-Centered Neuromuscular Control Perspective and Effects of Diaphragmatic Breathing Retraining

Combat sport athletes often need to maintain a guarded posture, stabilize the trunk, react quickly, and control balance during contact or unexpected movement. These demands may be related not only to strength and conditioning, but also to the coordination between breathing and postural control. The diaphragm is the main muscle for breathing and also contributes to trunk stability through its role in pressure regulation and deep core control. However, dysfunctional breathing patterns, such as upper-chest dominant breathing, reduced lower rib expansion, or poor coordination between the chest and abdomen, may interfere with this function.

The purpose of this study is to examine dysfunctional breathing patterns in combat sport athletes and to investigate whether diaphragmatic breathing retraining can improve breathing patterns, diaphragm function, core stability, postural control, and sport-related performance. This study will first screen athletes from combat and non-combat sports to determine the prevalence of dysfunctional breathing. Combat sport athletes will then complete laboratory tests to examine the relationship between breathing pattern, posture, diaphragm function, core stability, and postural control. In the intervention part of the study, combat sport athletes with dysfunctional breathing will be randomly assigned to diaphragmatic breathing retraining plus usual training or usual training only. The study will compare the two groups to determine whether adding diaphragmatic breathing retraining provides additional benefits. The study will also examine whether the changes are maintained after training and whether baseline measures can help identify athletes who respond better to the program.

調査の概要

詳細な説明

Combat sports place high demands on the neuromuscular system. Athletes must generate force, absorb impact, maintain balance, and respond to an opponent under rapidly changing conditions. Many combat sport athletes also use protective or guarded postures during training and competition. These postures may help with short-term stability, but they may also be associated with altered trunk control, reduced movement adaptability, and increased loading on the spine and surrounding tissues.

Breathing mechanics may be one factor related to these movement-control demands. The diaphragm is not only the primary muscle for inspiration, but also contributes to trunk stabilization. Through its interaction with the abdominal wall, pelvic floor, and deep spinal muscles, the diaphragm helps regulate intra-abdominal pressure and support postural control. When breathing is dominated by the upper chest or accessory muscles, the coordination between breathing and trunk stabilization may be less efficient.

Dysfunctional breathing has been reported in physically active and athletic populations, but its role in combat sport athletes is still not well understood. Most sport-related breathing studies have focused on respiratory muscle strength or endurance. Less attention has been given to breathing pattern normalization and the integration of breathing with postural control. For this reason, the present study focuses on dysfunctional breathing as a possible neuromuscular control issue rather than only a respiratory problem.

This study includes three main stages. In the first stage, athletes from combat and non-combat sports will be screened for dysfunctional breathing and postural characteristics. This stage will estimate the prevalence of dysfunctional breathing and compare breathing patterns between sport types. A subgroup of combat sport athletes will also complete laboratory-based testing to examine whether breathing pattern is associated with diaphragm function, posture, core stability, and postural control.

In the second stage, combat sport athletes with dysfunctional breathing will participate in an intervention study. Participants will first complete a single-session breathing correction assessment to examine immediate changes in breathing pattern and diaphragm function. They will then be randomly assigned to either diaphragmatic breathing retraining plus usual training or usual training only. The breathing retraining program will last 8 weeks and will progress from breathing correction in supported positions to breathing control in upright and core-demanding positions.

Assessments will be performed before the intervention, after the first breathing correction session, after the 8-week intervention, and at follow-up. The assessments will include breathing pattern evaluation, ultrasound assessment of diaphragm function, respiratory muscle strength testing, movement analysis, force plate testing, muscle activity recording, and functional sport performance tests. These tests are used to examine whether changes in breathing are accompanied by changes in trunk control, balance responses, and sport-related function.

In the third stage, the study will explore why some athletes improve more than others. Athletes who receive diaphragmatic breathing retraining will be classified as responders or non-responders based on changes in breathing pattern. Baseline breathing severity, diaphragm function, posture, core stability, postural control, and low back pain status will be examined as possible factors related to training response.

Overall, this study aims to clarify the relationship between breathing pattern and movement control in combat sport athletes. The findings may help determine whether diaphragmatic breathing retraining can be used as a practical strategy to improve breathing control, trunk stability, postural control, and sport-related performance in athletes with dysfunctional breathing.

研究の種類

介入

入学 (推定)

60

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

      • Tainan、台湾、701
        • 募集
        • Department of Physical Therapy, National Cheng Kung University,
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  • Aged between 18 and 50 years.
  • Currently participating regularly in combat sports, such as taekwondo, boxing, judo, karate, jiu-jitsu, or similar sports, with at least 2 years of training experience.
  • Training at least 3 times per week.

Exclusion Criteria:

  • Current or major musculoskeletal injury within the past year that may affect testing or training performance.
  • History of major thoracic, abdominal, or spinal surgery.
  • Known cardiopulmonary diseases, such as asthma, chronic obstructive pulmonary disease, or heart disease; neurological disorders; vestibular dysfunction; or other conditions that may affect balance.
  • Current or recent pregnancy.
  • Previous participation in breathing training or respiratory therapy, or current use of medications that may affect respiratory or neuromuscular function.
  • Inability to complete ultrasound assessment, motion analysis, or exercise testing.
  • Having a subordinate relationship or conflict of interest with the principal investigator or co-investigators, such as being a supervised student, research assistant, employee, or other related personnel.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Diaphragmatic Breathing Retraining Group
Combat sport athletes with dysfunctional breathing patterns will receive supervised diaphragmatic breathing training.
Participants will complete one session of diaphragmatic breathing correction. During the session, verbal instruction, manual facilitation, and corrective feedback will be used to guide participants toward a more diaphragmatic breathing pattern. Participants will be instructed to breathe with relaxed shoulders and neck, increase lower rib cage and abdominal expansion, and minimize upper-chest dominant breathing. The intervention is designed to examine the immediate effects of breathing correction on breathing pattern characteristics, diaphragm function, postural alignment, and core stability-related outcomes.
他の:Usual Training Control Group
Combat sport athletes in the control group will continue their usual sport-specific training without any structured breathing intervention. They will receive non-specific limb stretching and general exercise education.
Participants continue their regular sport-specific training schedule. They receive non-specific limb stretching and general exercise education but no structured breathing exercises or breathing instruction during the study period.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Breathing Pattern_ Total Faulty Breathing Scale (TFBS) Score
時間枠:Baseline (Day 1), Day 1 (immediately after first session), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Breathing pattern severity assessed using the Total Faulty Breathing Scale (TFBS), a structured observational tool scored 0-12. Higher scores indicate greater breathing dysfunction. Assessed during 10 cycles of quiet and 10 cycles of deep breathing in standing. Also supported by Manual Assessment of Respiratory Motion (MARM).
Baseline (Day 1), Day 1 (immediately after first session), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Trunk Flexor Endurance _ McGill Curl-Up Hold Test
時間枠:Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)

Description: Isometric trunk flexor endurance measured as hold time during the McGill Curl-Up Test. A longer time indicates greater endurance.

Unit of Measure: seconds

Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Back Extensor Endurance _Biering-Sørensen Test
時間枠:Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)

Isometric back extensor endurance measured as hold time during the Biering-Sørensen Test. A longer time indicates greater endurance.

Unit of Measure: seconds

Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Movement Speed_10-Meter Sprint Time
時間枠:Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)

Time to complete a 10-meter maximal sprint from a combat/two-point stance, measured with electronic timing gates. Lower time indicates better performance.

Unit of Measure: seconds

Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Agility _ T-Test Time
時間枠:Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)

Time to complete the agility T-test course (sprint forward, lateral shuffles, backward run around 4 cones in a T-shape). Lower time indicates better multidirectional agility.

Unit of Measure: seconds

Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Visual Motor Reaction Time _ BlazePod System
時間枠:Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)

Average reaction time to randomly illuminated light pods during a standardized protocol from a fighting stance, using the BlazePod system (BlazePod Ltd.). Lower time indicates faster reaction.

Unit of Measure: milliseconds

Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Dynamic Balance _ Y Balance Test Composite Score
時間枠:Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)

Maximum normalized reach distance in the anterior, posteromedial, and posterolateral directions during single-leg stance on the Y-Balance Test.

Unit of Measure: percent of leg length

Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Reactive Postural Control - Time to Stabilization
時間枠:Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Time to stabilization of center of pressure after an unexpected anterior pulling perturbation (10% body weight), measured via force plate. Lower time indicates better reactive postural control. Unit of Measure: seconds
Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Reactive Postural Control - Trunk/Pelvis Angular Displacement
時間枠:Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Angular displacement of the trunk and pelvis during the stabilization phase following an unexpected anterior pulling perturbation, measured via 3D motion capture. Unit of Measure: degrees
Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Reactive Postural Control - Trunk/Pelvis Angular Velocity
時間枠:Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Angular velocity of the trunk and pelvis during the stabilization phase following an unexpected anterior pulling perturbation, measured via 3D motion capture. Unit of Measure: degrees per second
Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Reactive Postural Control - Peak Ground Reaction Force
時間枠:Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Peak ground reaction force during the stabilization phase following an unexpected anterior pulling perturbation, measured via force plate. Unit of Measure: percent of body weight
Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Reactive Postural Control - COP Path Length
時間枠:Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Total center-of-pressure trajectory length during the stabilization phase following an unexpected anterior pulling perturbation, measured via force plate and normalized to foot length. Unit of Measure: mm
Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Reactive Postural Control - Trunk Muscle Onset Latency
時間枠:Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
EMG onset latency of trunk muscles relative to perturbation onset, measured via surface electromyography. Unit of Measure: milliseconds
Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Reactive Postural Control - Trunk Muscle EMG Amplitude
時間枠:Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Normalized EMG amplitude of trunk muscles during the early stabilization phase following an unexpected anterior pulling perturbation. Unit of Measure: percent of MVIC
Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Maximal Inspiratory Pressure (MIP)
時間枠:Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion) Secondary
Global inspiratory muscle strength was measured in cmH₂O using a gas pressure gauge (Galemed Corporation). Participants exhale maximally, then inhale forcefully against the gauge for ≥1 second with a nose clip applied.
Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion) Secondary
Maximal Expiratory Pressure (MEP)
時間枠:Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)

Global expiratory muscle strength is measured using a gas pressure gauge. Participants inhale maximally, then exhale forcefully against the gauge for ≥1 second.

Unit of Measure: cmH₂O

Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Diaphragmatic Excursion
時間枠:Baseline (Day 1), Day 1 (immediately after first session), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)

Maximum diaphragmatic excursion during maximal inspiration and expiration, measured by M-mode ultrasonography with a 1-5 MHz convex transducer in the right mid-clavicular subcostal region.

Unit of Measure: cm

Baseline (Day 1), Day 1 (immediately after first session), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Diaphragmatic Thickening Fraction
時間枠:Baseline (Day 1), Day 1 (immediately after first session), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)

Diaphragmatic thickening fraction calculated from B-mode ultrasound measurements of diaphragm thickness at end-maximal inspiration and end-maximal expiration, using a 4-12 MHz linear transducer at the zone of apposition.

Unit of Measure: percent

Baseline (Day 1), Day 1 (immediately after first session), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Proactive Core Stability - Time to Stabilization
時間枠:Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Time to stabilization of center of pressure after single-leg drop landing, measured via force plate. Lower time indicates better proactive core stability. Unit of Measure: seconds
Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Proactive Core Stability - Trunk/Pelvis Angular Displacement
時間枠:Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Angular displacement of the trunk and pelvis during the stabilization phase following single-leg drop landing, measured via 3D motion capture. Unit of Measure: degrees
Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Proactive Core Stability - Trunk/Pelvis Angular Velocity
時間枠:Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Angular velocity of the trunk and pelvis during the stabilization phase following single-leg drop landing, measured via 3D motion capture. Unit of Measure: degrees per second
Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Proactive Core Stability - Peak Ground Reaction Force
時間枠:Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Peak ground reaction force during the stabilization phase following single-leg drop landing, measured via force plate. Unit of Measure: percent of body weight
Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Proactive Core Stability - COP Path Length
時間枠:Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Total center-of-pressure trajectory length during the stabilization phase following single-leg drop landing, measured via force plate and normalized to foot length. Unit of Measure: mm
Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Proactive Core Stability - Trunk Muscle EMG Amplitude
時間枠:Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)
Normalized EMG amplitude of trunk muscles during the early stabilization phase following single-leg drop landing. Unit of Measure: percent of MVIC
Baseline (Day 1), Week 8 (post-intervention), Week 16 (8 weeks after intervention completion)

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2026年5月1日

一次修了 (推定)

2029年7月1日

研究の完了 (推定)

2029年7月1日

試験登録日

最初に提出

2026年7月2日

QC基準を満たした最初の提出物

2026年7月15日

最初の投稿 (実際)

2026年7月21日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月21日

QC基準を満たした最後の更新が送信されました

2026年7月15日

最終確認日

2026年7月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

購読する