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临床试验/NCT07046637
NCT07046637尚未招募不适用

Short-Term Effects of Inspiratory Muscle Warm-Up and Fatigue on Diaphragmatic Function in Professional Basketball Players: A Randomized Controlled Trial

Sierra Varona SL0 个研究点目标入组 38 人开始时间: 2025年7月10日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
38
主要终点
Maximal inspiratory pressure

研究概览

简要总结

This randomized controlled trial investigates the acute effects of inspiratory muscle warm-up and fatigue on diaphragmatic function in professional basketball players. Using ultrasound imaging and maximal inspiratory pressure (PIM) assessment, the study evaluates changes in diaphragmatic thickness and respiratory strength before and after specific inspiratory muscle loading protocols. Findings aim to clarify the short-term impact of these interventions on diaphragmatic recovery capacity, with potential implications for respiratory training, performance enhancement, and injury prevention strategies in elite athletic populations.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

盲法说明

Single-blind

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Male and female professional basketball players aged between 18 and 35 years.
  • Holding a valid federation license at the autonomous or higher competitive level.
  • A minimum of 3 consecutive seasons of competition in official FEB, FIBA, or equivalent regional leagues.
  • Regular training frequency of ≥4 sessions per week over the past 6 months.
  • No previous experience with inspiratory muscle training.
  • Ability to understand study procedures and provide written informed consent.

排除标准

  • History of chronic respiratory, neuromuscular, or cardiovascular disease.
  • Musculoskeletal injury limiting inspiratory effort or physical participation (current or within the past three months).
  • Previous thoracic or abdominal surgery.
  • Current smokers.
  • Use of pharmacological treatments that could affect respiratory or muscular function.
  • Participation in another interventional study within the past 4 weeks.
  • Inability to understand or follow study instructions.
  • Tympanic membrane perforation or middle/inner ear pathology.
  • Pregnancy or postpartum period within the last 6 months.

结局指标

主要结局

Maximal inspiratory pressure

时间窗: Immediately before intervention, immediately after intervention, 15 minutes post intervention and 30 minutes post intervention

It will be assessed using a Breathare MIP/MEP® (GH Innotek Co., Ltd., Busan, Republic of Korea).The Breathare MIP/MEP® is likely a respiratory pressure meter or manometer designed for measuring respiratory muscle strength. It typically includes a mouthpiece connected to a pressure sensor, and the device measures the force or pressure generated during respiratory maneuvers. The person will be instructed to take a maximal deep breath in, and then exhale to residual volume. After that, they will be asked to inhale forcefully against the resistance provided by the Breathare MIP/MEP®. This measures the strength of the inspiratory muscles. The measures will be expressed in cmH2O.

Maximal inspiratory pressure

时间窗: Immediately before intervention, immediately after intervention, 15 minutes post intervention and 30 minutes post intervention

It will be assessed using a Breathare MIP/MEP® (GH Innotek Co., Ltd., Busan, Republic of Korea).The Breathare MIP/MEP® is likely a respiratory pressure meter or manometer designed for measuring respiratory muscle strength. It typically includes a mouthpiece connected to a pressure sensor, and the device measures the force or pressure generated during respiratory maneuvers. The person will be instructed to take a maximal deep breath in, and then exhale to residual volume. After that, they will be asked to inhale forcefully against the resistance provided by the Breathare MIP/MEP®. This measures the strength of the inspiratory muscles. The measures will be expressed in cmH2O.

次要结局

  • Diaphragmatic thickness and thickening fraction(Immediately before intervention, immediately after intervention, 15 minutes post intervention and 30 minutes post intervention)

研究者

申办方类型
Other
责任方
Sponsor

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