Circadian Modulation of Neurophysiological Responses to Therapeutic Massage Modalities

January 17, 2026 updated by: Monira Aldhahi, Princess Nourah Bint Abdulrahman University

Circadian Modulation of Neurophysiological Responses to Therapeutic Massage Modalities in Taekwondo Athletes: A Randomized Crossover Trial

Athletic performance and recovery are closely linked to central nervous system regulation, which can be objectively assessed using electroencephalography (EEG). Although therapeutic massage is widely used as a recovery modality in combat sports, its neurophysiological effects and potential interaction with circadian timing remain poorly understood. This study investigates whether different therapeutic massage modalities applied at different times of the day modulate resting-state EEG activity in taekwondo athletes.

Study Overview

Status

Completed

Conditions

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

Interventional

Enrollment (Actual)

12

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Malatya, Turkey (Türkiye)
        • Faculty of Sport Sciences, İnönü University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 1, 2025

Primary Completion (Actual)

January 1, 2026

Study Completion (Actual)

January 5, 2026

Study Registration Dates

First Submitted

January 17, 2026

First Submitted That Met QC Criteria

January 17, 2026

First Posted (Actual)

January 26, 2026

Study Record Updates

Last Update Posted (Actual)

January 26, 2026

Last Update Submitted That Met QC Criteria

January 17, 2026

Last Verified

January 1, 2026

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)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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