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CompletedNCT07892118Updated Oct 23, 2026

Effects of Sports Massage and Thai Massage on Delayed-Onset Muscle Soreness and Recovery

An interventional study of Sports Massage and Traditional Thai Massage in Delayed Onset Muscle Soreness (DOMS), sponsored by Akdeniz University. Completed at 1 site in Turkey (Türkiye). Open to male participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-23.

Sponsored by Akdeniz University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 2 years 10 months after the study started (first participant enrolled Dec 2023, registered Oct 2026).
Updated Oct 23, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
35
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
Male
01

Study summary

This study investigated the effects of sports massage and modified traditional Thai massage on delayed-onset muscle soreness (DOMS) and recovery following strenuous exercise in healthy, physically inactive young men.

The study used a randomized, three-condition, three-period crossover design. Participants completed an exercise protocol designed to induce muscle soreness and subsequently received one of three recovery interventions: sports massage, modified traditional Thai massage, or passive recovery. Each participant underwent all three conditions in a randomized sequence, with a washout period between experimental sessions.

The recovery interventions were administered approximately six hours after exercise. Muscle soreness, pressure pain threshold, flexibility, vertical jump performance, and perceived physical performance were assessed at baseline and at 24 and 48 hours after exercise.

The study aimed to compare the effects of the two massage approaches with passive recovery on perceived muscle soreness, mechanical pain sensitivity, and functional recovery following exercise-induced muscle damage.

02

Conditions studied

  • Delayed Onset Muscle Soreness (DOMS)

Keywords

  • Delayed Onset Muscle Soreness
  • Sports Massage
  • Thai Massage
  • Plyometric Exercise
  • Recovery
03

In context

Lead sponsor

Akdeniz University is the lead sponsor of 296 studies on the registry; 62 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Healthy male volunteers aged 18-30 years.
  • Physically inactive or sedentary individuals who did not regularly participate in structured exercise or sports training.
  • Ability and willingness to complete the exercise protocol, recovery interventions, and follow-up assessments.
  • Provision of written informed consent.

Exclusion criteria

Exclusion Criteria:

  • Lower-extremity musculoskeletal injury within the preceding six months.
  • Regular participation in structured exercise or sports training.
  • Medical conditions or positive responses on the Physical Activity Readiness Questionnaire (PAR-Q) indicating that participation in the exercise protocol could be unsafe.
  • Contraindications to massage or strenuous physical exercise.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
35 participants (actual)

Study arms

  • Experimental
    Sequence ABC: Sports Massage → Thai Massage → Passive Recovery

    Participants assigned to Sequence ABC received sports massage in Period 1, traditional Thai massage in Period 2, and passive recovery in Period 3. Each intervention lasted 20 minutes and was administered approximately six hours after the standardized plyometric exercise protocol. Experimental periods were separated by an approximately one-week washout interval.

    Procedure: Sports Massage · Procedure: Traditional Thai Massage · Other: Passive Recovery

  • Experimental
    Sequence ACB: Sports Massage → Passive Recovery → Thai Massage

    Participants assigned to Sequence ACB received sports massage in Period 1, passive recovery in Period 2, and traditional Thai massage in Period 3. Each intervention lasted 20 minutes and was administered approximately six hours after the standardized plyometric exercise protocol. Experimental periods were separated by an approximately one-week washout interval.

    Procedure: Sports Massage · Procedure: Traditional Thai Massage · Other: Passive Recovery

  • Experimental
    Sequence BAC: Thai Massage → Sports Massage → Passive Recovery

    Participants assigned to Sequence BAC received traditional Thai massage in Period 1, sports massage in Period 2, and passive recovery in Period 3. Each intervention lasted 20 minutes and was administered approximately six hours after the standardized plyometric exercise protocol. Experimental periods were separated by an approximately one-week washout interval.

    Procedure: Sports Massage · Procedure: Traditional Thai Massage · Other: Passive Recovery

  • Experimental
    Sequence BCA: Thai Massage → Passive Recovery → Sports Massage

    Participants assigned to Sequence BCA received traditional Thai massage in Period 1, passive recovery in Period 2, and sports massage in Period 3. Each intervention lasted 20 minutes and was administered approximately six hours after the standardized plyometric exercise protocol. Experimental periods were separated by an approximately one-week washout interval.

    Procedure: Sports Massage · Procedure: Traditional Thai Massage · Other: Passive Recovery

  • Experimental
    Sequence CAB: Passive Recovery → Sports Massage → Thai Massage

    Participants assigned to Sequence CAB received passive recovery in Period 1, sports massage in Period 2, and traditional Thai massage in Period 3. Each intervention lasted 20 minutes and was administered approximately six hours after the standardized plyometric exercise protocol. Experimental periods were separated by an approximately one-week washout interval.

    Procedure: Sports Massage · Procedure: Traditional Thai Massage · Other: Passive Recovery

  • Experimental
    Sequence CBA: Passive Recovery → Thai Massage → Sports Massage

    Participants assigned to Sequence CBA received passive recovery in Period 1, traditional Thai massage in Period 2, and sports massage in Period 3. Each intervention lasted 20 minutes and was administered approximately six hours after the standardized plyometric exercise protocol. Experimental periods were separated by an approximately one-week washout interval.

    Procedure: Sports Massage · Procedure: Traditional Thai Massage · Other: Passive Recovery

Interventions

  • ProcedureSports Massage

    A standardized 20-minute sports massage was administered to the lower extremities approximately six hours after the plyometric exercise protocol. The intervention included manual massage techniques applied to the major lower-extremity muscle groups, following a standardized treatment protocol.

  • ProcedureTraditional Thai Massage

    A standardized 20-minute modified traditional Thai massage protocol was administered to the lower extremities approximately six hours after the plyometric exercise protocol. The intervention incorporated Thai massage techniques adapted for the study, including manual pressure and assisted stretching techniques targeting the major lower-extremity muscle groups.

  • OtherPassive Recovery

    Participants rested quietly in the supine position for 20 minutes without receiving massage, stretching, or any other recovery intervention. The passive recovery session was conducted approximately six hours after the standardized plyometric exercise protocol.

06

What researchers measure

Primary outcomes

  1. Change From Baseline in Muscle Soreness at 24 and 48 Hours

    Muscle soreness at rest was assessed using an 11-point Numerical Rating Scale (NRS-11), ranging from 0 (no pain) to 10 (worst imaginable pain). Measurements were obtained before the plyometric exercise protocol and at 24 and 48 hours after exercise in each of the three experimental periods. Changes from baseline were compared among sports massage, traditional Thai massage, and passive recovery conditions. Higher scores indicate greater perceived muscle soreness.

    Time frame: Baseline (before exercise), 24 hours, and 48 hours after exercise in each experimental period

Secondary outcomes

  1. Change From Baseline in Sit-and-Reach Flexibility at 24 and 48 Hours

    Flexibility was assessed using the Sit-and-Reach test, with results recorded in centimeters (cm). Participants performed three trials with their knees extended, and the best result was retained for analysis. Changes from baseline were evaluated at 24 and 48 hours after exercise for each recovery condition. Higher values indicate greater reach distance.

    Time frame: Baseline (before exercise), 24 hours, and 48 hours after exercise in each experimental period

  2. Change From Baseline in Hands-Free Vertical Jump Height at 24 and 48 Hours

    Vertical jump performance was assessed using the Optojump system. Participants performed countermovement jumps with unrestricted arm movement (hands-free condition). Two valid attempts were performed, and the highest jump height was retained for analysis. Jump height was recorded in centimeters (cm). Measurements were obtained at baseline and at 24 and 48 hours after exercise in each experimental period. Higher values indicate greater vertical jump performance. Kopyala

    Time frame: Baseline (before exercise), 24 hours, and 48 hours after exercise in each experimental period

  3. Change From Baseline in Hands-on-Hips Vertical Jump Height at 24 and 48 Hours

    Vertical jump performance was assessed using the Optojump system. Participants performed countermovement jumps with their hands maintained on their hips throughout the movement to minimize the contribution of arm swing. Two valid attempts were performed, and the highest jump height was retained for analysis. Jump height was recorded in centimeters (cm). Measurements were obtained at baseline and at 24 and 48 hours after exercise in each experimental period. Higher values indicate greater vertical jump performance.

    Time frame: Baseline (before exercise), 24 hours, and 48 hours after exercise in each experimental period

  4. Change From Baseline in Perceived Physical Performance at 24 and 48 Hours

    Perceived physical performance was assessed immediately after the vertical jump tests using a participant-reported 10-point rating scale. Participants were asked to rate how they perceived their jumping performance, with scores ranging from 1 (very poor performance) to 10 (excellent performance). The assessment was repeated during the baseline, 24-hour, and 48-hour testing sessions in each experimental period. Higher scores indicate better perceived physical performance. Changes from baseline were compared among the sports massage, traditional Thai massage, and passive recovery conditions.

    Time frame: Baseline (before exercise), 24 hours, and 48 hours after exercise in each experimental period

  5. Change From Baseline in Pressure Pain Threshold of the Right Quadriceps at 24 and 48 Hours

    Pressure pain threshold (PPT) was measured over the right quadriceps muscle region using a pressure algometer. Pressure was gradually increased until the participant first reported pain. Two measurements were obtained approximately 30 seconds apart, and the lower value was retained for analysis. Assessments were performed at baseline and at 24 and 48 hours after exercise in each experimental period. Higher PPT values indicate lower pressure pain sensitivity. Pressure pain threshold (PPT) was measured over the \[anatomical region\] using a pressure algometer. Pressure was gradually increased until the participant first reported pain. Two measurements were obtained approximately 30 seconds apart, and the lower value was retained for analysis. PPT was expressed in kilograms per square centimeter (kg/cm²). Assessments were performed at baseline and at 24 and 48 hours after exercise in each experimental period. Higher PPT values indicate lower pressure pain sensitivity.

    Time frame: Baseline (before exercise), 24 hours, and 48 hours after exercise in each experimental period.

  6. Change From Baseline in Pressure Pain Threshold of the Left Quadriceps at 24 and 48 Hours

    Pressure pain threshold (PPT) was measured over the left quadriceps muscle region using a pressure algometer. Pressure was gradually increased until the participant first reported pain. Two measurements were obtained approximately 30 seconds apart, and the lower value was retained for analysis. Assessments were performed at baseline and at 24 and 48 hours after exercise in each experimental period. Higher PPT values indicate lower pressure pain sensitivity. Pressure pain threshold (PPT) was measured over the \[anatomical region\] using a pressure algometer. Pressure was gradually increased until the participant first reported pain. Two measurements were obtained approximately 30 seconds apart, and the lower value was retained for analysis. PPT was expressed in kilograms per square centimeter (kg/cm²). Assessments were performed at baseline and at 24 and 48 hours after exercise in each experimental period. Higher PPT values indicate lower pressure pain sensitivity.

    Time frame: Baseline (before exercise), 24 hours, and 48 hours after exercise in each experimental period.

  7. Change From Baseline in Pressure Pain Threshold of the Right Hamstrings at 24 and 48 Hours

    Pressure pain threshold (PPT) was measured over the right hamstring muscle region using a pressure algometer. Pressure was gradually increased until the participant first reported pain. Two measurements were obtained approximately 30 seconds apart, and the lower value was retained for analysis. Assessments were performed at baseline and at 24 and 48 hours after exercise in each experimental period. Higher PPT values indicate lower pressure pain sensitivity. Pressure pain threshold (PPT) was measured over the \[anatomical region\] using a pressure algometer. Pressure was gradually increased until the participant first reported pain. Two measurements were obtained approximately 30 seconds apart, and the lower value was retained for analysis. PPT was expressed in kilograms per square centimeter (kg/cm²). Assessments were performed at baseline and at 24 and 48 hours after exercise in each experimental period. Higher PPT values indicate lower pressure pain sensitivity.

    Time frame: Baseline (before exercise), 24 hours, and 48 hours after exercise in each experimental period.

  8. Change From Baseline in Pressure Pain Threshold of the Left Hamstrings at 24 and 48 Hours

    Pressure pain threshold (PPT) was measured over the left hamstring muscle region using a pressure algometer. Pressure was gradually increased until the participant first reported pain. Two measurements were obtained approximately 30 seconds apart, and the lower value was retained for analysis. Assessments were performed at baseline and at 24 and 48 hours after exercise in each experimental period. Higher PPT values indicate lower pressure pain sensitivity. Pressure pain threshold (PPT) was measured over the \[anatomical region\] using a pressure algometer. Pressure was gradually increased until the participant first reported pain. Two measurements were obtained approximately 30 seconds apart, and the lower value was retained for analysis. PPT was expressed in kilograms per square centimeter (kg/cm²). Assessments were performed at baseline and at 24 and 48 hours after exercise in each experimental period. Higher PPT values indicate lower pressure pain sensitivity.

    Time frame: Baseline (before exercise), 24 hours, and 48 hours after exercise in each experimental period.

  9. Change From Baseline in Pressure Pain Threshold of the Right Calf at 24 and 48 Hours

    Pressure pain threshold (PPT) was measured over the right calf muscle region using a pressure algometer. Pressure was gradually increased until the participant first reported pain. Two measurements were obtained approximately 30 seconds apart, and the lower value was retained for analysis. Assessments were performed at baseline and at 24 and 48 hours after exercise in each experimental period. Higher PPT values indicate lower pressure pain sensitivity. Pressure pain threshold (PPT) was measured over the \[anatomical region\] using a pressure algometer. Pressure was gradually increased until the participant first reported pain. Two measurements were obtained approximately 30 seconds apart, and the lower value was retained for analysis. PPT was expressed in kilograms per square centimeter (kg/cm²). Assessments were performed at baseline and at 24 and 48 hours after exercise in each experimental period. Higher PPT values indicate lower pressure pain sensitivity.

    Time frame: Baseline (before exercise), 24 hours, and 48 hours after exercise in each experimental period.

  10. Change From Baseline in Pressure Pain Threshold of the Left Calf at 24 and 48 Hours

    Pressure pain threshold (PPT) was measured over the left calf muscle region using a pressure algometer. Pressure was gradually increased until the participant first reported pain. Two measurements were obtained approximately 30 seconds apart, and the lower value was retained for analysis. Assessments were performed at baseline and at 24 and 48 hours after exercise in each experimental period. Higher PPT values indicate lower pressure pain sensitivity. Pressure pain threshold (PPT) was measured over the \[anatomical region\] using a pressure algometer. Pressure was gradually increased until the participant first reported pain. Two measurements were obtained approximately 30 seconds apart, and the lower value was retained for analysis. PPT was expressed in kilograms per square centimeter (kg/cm²). Assessments were performed at baseline and at 24 and 48 hours after exercise in each experimental period. Higher PPT values indicate lower pressure pain sensitivity.

    Time frame: Baseline (before exercise), 24 hours, and 48 hours after exercise in each experimental period.

07

Study locations

1 site
  • Akdeniz University
    Antalya, Antalya 07070, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: Undecided — The decision regarding sharing de-identified individual participant data (IPD) has not yet been finalized. The research team will review the feasibility and conditions of data sharing, including participant consent, ethical and institutional requirements, and data confidentiality safeguards, before making a final decision.

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Dec 2023 to primary completion in Jan 2024, 1 month.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 17, 2026
First posted
Oct 23, 2026
StartActual
Dec 11, 2023
Primary completionActual
Jan 31, 2024
CompletionActual
Jan 31, 2024
Last update
Oct 23, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 23, 2026
Show all 1 update
  1. Oct 23, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07892118
Lead sponsor
Akdeniz University
Responsible party
Sponsor
First posted
Oct 23, 2026
Start date
Dec 11, 2023
Primary completion
Jan 31, 2024
Completion
Jan 31, 2024
Last update
Oct 23, 2026

Study contacts

Nihat Ayçeman, PhD
principal investigator · Akdeniz University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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