Diaphragmatic Kinesio Taping With HIIT in Trained Individuals

NCT07390721 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2026-02-09

No results posted yet for this study

Summary

This study examines whether adding diaphragmatic kinesio taping to high-intensity interval training (HIIT) improves physical performance in trained individuals. Participants will be randomly assigned to one of two groups. One group will perform an 8-week HIIT program on a cycle ergometer. The other group will follow the same HIIT program and will also receive diaphragmatic kinesio taping before each exercise session. The taping is applied to support breathing muscles and may help improve oxygen use during exercise.

Before and after the training period, participants will undergo tests to measure aerobic capacity (VO₂max), anaerobic power (Wingate test), balance (Y-Balance test), lung function (spirometry), body composition, and heart rate responses. The results of this study will help determine whether diaphragmatic kinesio taping provides additional benefits when combined with HIIT training.

Conditions

  • Postural Balance
  • Physical Fitness
  • Healthy Volunteers

Interventions

BEHAVIORAL

High-Intensity Interval Training (HIIT)

Participants perform an 8-week supervised high-intensity interval training program on a cycle ergometer, three times per week. Each session includes warm-up, alternating high- and low-intensity intervals targeting 85-95% of maximal heart rate, and cool-down.

OTHER

Diaphragmatic Kinesio Taping

Elastic kinesio tape is applied to the diaphragmatic region before each training session using a standardized technique to support inspiratory muscle activity and facilitate breathing.

Sponsors & Collaborators

  • Health Institutes of Turkey

    collaborator OTHER_GOV
  • Uludag University

    collaborator OTHER
  • Agri Ibrahim Cecen University

    lead OTHER

Principal Investigators

  • Fadıl Özyener, Prof. Dr. · Uludag University

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-09-01
Primary Completion
2026-11-30
Completion
2026-12-30

Countries

  • Turkey (Türkiye)

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07390721 on ClinicalTrials.gov