- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07367607
Circadian Modulation of Neurophysiological Responses to Therapeutic Massage Modalities
Circadian Modulation of Neurophysiological Responses to Therapeutic Massage Modalities in Taekwondo Athletes: A Randomized Crossover Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This randomized, within-subject crossover study examines the effects of different therapeutic massage modalities and time of day on resting-state EEG activity in elite male taekwondo athletes. Twelve athletes complete four experimental conditions: no-massage control, friction massage, vibration mechanical massage, and percussion mechanical massage. Each condition is administered during both morning and evening sessions, separated by a minimum 48-hour washout period.
Resting-state EEG is recorded immediately following each intervention using a 32-channel system. Power spectral density is computed to extract global band power in delta, theta, alpha, beta, and gamma frequency bands. The study aims to determine whether massage modality, circadian timing, or their interaction significantly influences cortical oscillatory activity associated with recovery and neural readiness.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Malatya, Turkey (Türkiye)
- Faculty of Sport Sciences, İnönü University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Male taekwondo athletes aged 18-25 years
- Minimum of 4 years of structured taekwondo training
- Training frequency ≥ 5 days/week
- Black belt (1st Dan or higher)
- No musculoskeletal injury in the past 6 months
Exclusion Criteria:
- Neurological or psychiatric disorders
- Use of stimulant substances or anti-inflammatory medication
- Irregular sleep-wake patterns (e.g., shift work)
- Withdrawal of consent at any stage
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Friction Massage (FMP)
|
Manual therapeutic massage consisting of rhythmic, sustained friction techniques applied by a certified physiotherapist to the dominant upper extremity muscles.
Moderate-to-strong pressure was applied for a total duration of 10 minutes using a standardized intermittent protocol.
|
|
Experimental: Vibration Mechanical Massage (VMMP)
|
Therapeutic vibration massage delivered using a handheld vibration device set at a fixed frequency of 50 Hz.
The device was applied to the dominant upper extremity muscles for 10 minutes to provide localized high-frequency mechanical stimulation.
|
|
Experimental: Percussion Mechanical Massage (PMMP)
|
Therapeutic percussion massage administered using a handheld percussive therapy device delivering rapid mechanical impulses at approximately 40 Hz.
The intervention was applied to the dominant upper extremity muscles for 10 minutes to elicit deep somatosensory stimulation.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Global EEG Band Power
Time Frame: Immediately post-intervention in morning and evening sessions.
|
Log-transformed power spectral density values for delta, theta, alpha, beta, and gamma frequency bands obtained from resting-state EEG recordings.
|
Immediately post-intervention in morning and evening sessions.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Topographical EEG Distribution
Time Frame: Immediately post-intervention in morning and evening sessions.
|
Spatial distribution of EEG band power across frontal and central scalp regions.
|
Immediately post-intervention in morning and evening sessions.
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PNU-10
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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