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NCT07652398
Effects of Passive Recovery Methods After High-Intensity Cycling Exercise
Conditions: Young Adult Health, Young Adults
Sex: Female
Ages: 18 Years – 30 Years
Healthy volunteers: Yes
Phase: NA
Enrollment: 12
Sponsor: Pamukkale University
Location: Pamukkale University, Faculty of Physiotherapy and Rehabilitation Denizli
Summary
This randomized crossover trial will investigate the acute effects of five passive recovery interventions following a standardized high-intensity cycling exercise protocol. Participants will complete the standardized high-intensity cycling exercise protocol during five separate study sessions. Immediately after each exercise session, participants will receive one of five recovery interventions: compression therapy, vacuum therapy, kinesiology taping, passive rest, or classical massage. The order of the interventions will be randomized according to a balanced crossover sequence. Each participant will experience all five recovery interventions during the study period. Outcomes related to post-exercise recovery will be assessed across intervention periods.
Eligibility Criteria
Inclusion Criteria:
* Healthy adult volunteers aged 18-30 years
* Able to perform high-intensity cycling exercise
* No musculoskeletal injury within the last six months
* No known cardiovascular, neurological, or metabolic disease
* Not using medication that may affect exercise performance, pain perception, or recovery
* Willing to attend all five study sessions
* Willing to receive all five passive recovery interventions
* Provided written informed consent
Exclusion Criteria:
* Presence of acute or chronic musculoskeletal injury
* History of cardiovascular, neurological, respiratory, or metabolic disease
* Contraindication to high-intensity exercise
* Contraindication to compression therapy, vacuum therapy, kinesiology taping, passive rest, or classical massage
* Skin allergy, open wound, dermatological disease, or sensitivity to kinesiology tape
* Use of analgesic, anti-inflammatory, muscle relaxant, or performance-enhancing medication during the study period
* Participation in another exercise or recovery intervention study during the study period
* Failure to attend all study sessions or comply with study procedures
Source: ClinicalTrials.gov (NCT07652398). StuddyBuddy aggregates publicly available trial information.