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Recruiting NCT07352722

NCT07352722 Intercostal Mobilization and Respiratory Outcomes

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Clinical Trial Summary
NCT ID NCT07352722
Status Recruiting
Phase
Sponsor Abant Izzet Baysal University
Condition Healthy Volunteers
Study Type INTERVENTIONAL
Enrollment 90 participants
Start Date 2025-10-15
Primary Completion 2026-06-01

Trial Parameters

Condition Healthy Volunteers
Sponsor Abant Izzet Baysal University
Study Type INTERVENTIONAL
Phase N/A
Enrollment 90
Sex ALL
Min Age 18 Years
Max Age 30 Years
Start Date 2025-10-15
Completion 2026-06-01
Interventions
Intercostal mobilizationSham intercostal mobilizationRest

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Brief Summary

This cross-sectional study was planned to investigate the effects of intercostal mobilization on respiratory muscle strength, pulmonary function parameters, and performance in the ascending speed shuttle walking test. The study will be conducted in a prospective, randomized, controlled and double-blind design. A total of 90 healthy volunteers aged between 18-30 years with a sedentary lifestyle will be included in the study. The individuals will be divided into 3 groups as Intercostal Mobilization Group (n=30), Sham Application Group (n=30) and Control Group (n=30) by simple randomization. Sociodemographic Data Form, Sedentary Behavior Questionnaire, Pulmonary Function Test, Respiratory Muscle Strength Measurement (MIP/MEP), Incremental Shuttle Walking Test will be applied to the individuals before the intervention. After the intervention, only pulmonary function tests, respiratory muscle strength measurement and ISWT will be repeated. The study results are expected to contribute to the development of new evidence-based approaches to respiratory rehabilitation

Eligibility Criteria

Inclusion Criteria: * Be between 18 and 30 years old, * Have a sedentary lifestyle, * Be willing to participate in the study Exclusion Criteria: * History of neurological, orthopedic, or cardiopulmonary disease that could affect respiratory function, * Refusal to participate in the study

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