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CompletedNCT07808814Updated Sep 9, 2026

Portable Low-Level Laser Therapy for Recovery After a Quadriceps-Dominant Fatiguing Task in Recreational Runners

An interventional study of LLLT and Sham in Muscle Fatigue Caused by Repetitive Muscle Exercise, sponsored by Chia Nan University of Pharmacy & Science. Completed at 1 site in Taiwan. Open to male participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-09.

Sponsored by Chia Nan University of Pharmacy & Science · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Registered 1 year 6 months after the study started (first participant enrolled Feb 2025, registered Sep 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
Male
01

Study summary

This randomized, sham-controlled, two-period crossover study evaluated the effects of portable 808-nm low-level laser therapy (LLLT) on acute recovery and running biomechanics following a quadriceps-dominant fatiguing task in recreational runners. Twenty male recreational runners completed both active LLLT and sham conditions, separated by a 2-week washout period. After the fatiguing task, participants received 10 minutes of bilateral quadriceps LLLT or sham treatment, followed by treadmill running at the same fixed self-selected speed. Quadriceps soreness, heart rate, running spatiotemporal parameters, and kinematic responses were assessed using a verbal numerical rating scale, heart-rate monitoring, two-dimensional video analysis, and inertial measurement units.

Read the detailed description

Each participant completed two experimental visits in randomized order, with one active LLLT condition and one sham condition separated by a 2-week washout period. At each visit, participants completed a 5-minute treadmill warm-up followed by a 3-minute pre-fatigue running trial at a fixed self-selected running speed. They then performed a repeated stand-sit-stand task designed to produce quadriceps-dominant lower-limb fatigue.

Immediately after the fatiguing task, participants received either active portable 808-nm LLLT or sham treatment for 10 minutes over the bilateral rectus femoris, vastus lateralis, and vastus medialis muscles. A 3-minute post-intervention treadmill running trial was then performed at the same running speed used before the fatiguing task.

Quadriceps soreness was assessed using a 0-10 verbal numerical rating scale. Heart rate was monitored using a chest-strap heart-rate monitor. Running spatiotemporal and kinematic variables were assessed using high-frame-rate two-dimensional video analysis and three inertial measurement units positioned over the bilateral distal tibiae and sacral region.

02

Conditions studied

  • Muscle Fatigue Caused by Repetitive Muscle Exercise

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Keywords

  • Running Biomechanics
  • Inertial Measurement Units
  • Low-Level Laser Therapy
  • Photobiomodulation Therapy
  • Recreational Runners
03

In context

Fatigue

2,229 studies on the registry are indexed under Fatigue; 426 are open to participants now.

This study's enrollment of 20 is below the median of 54 across 1,757 interventional studies indexed under Fatigue.

Browse Fatigue studies →

Lead sponsor

Chia Nan University of Pharmacy & Science is the lead sponsor of 6 studies on the registry; none are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 40 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

  1. Male recreational runners aged 18-40 years.
  2. Recreational running status determined using the World Masters Athletics (WMA) age-graded performance score, with an age-graded score below 60%.
  3. Previous experience with treadmill running.
  4. Rearfoot-strike running pattern.
  5. No running-related lower-limb injury during the preceding 6 months

Exclusion criteria

Exclusion Criteria:

  1. WMA age-graded performance score of 60% or higher.
  2. Non-rearfoot-strike running pattern.
  3. Leg-length discrepancy greater than 3 cm.
  4. Use of an orthosis, brace, or other lower-limb medical device that could influence running gait.
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
20 participants (actual)

Study arms

  • Experimental
    LLLT-Sham Sequence

    Participants received LLLT during the first experimental period and sham during the second experimental period, with a 2-week washout period between visits.

    Device: LLLT · Device: Sham

  • Experimental
    Sham-LLLT Sequence

    Participants received sham during the first experimental period and LLLT during the second experimental period, with a 2-week washout period between visits.

    Device: LLLT · Device: Sham

Interventions

  • DeviceLLLT

    Portable 808-nm low-level laser therapy applied bilaterally to the rectus femoris, vastus lateralis, and vastus medialis for 10 minutes.

  • DeviceSham

    Sham device applied to the same bilateral quadriceps sites for 10 minutes, matching the LLLT condition in device appearance, placement, duration, and fixation.

06

What researchers measure

Primary outcomes

  1. Quadriceps Soreness

    Quadriceps soreness was assessed using a 0-10 verbal numerical rating scale (VNRS), where 0 indicated no soreness and 10 indicated the worst imaginable soreness. Decimal responses were permitted.

    Time frame: Immediately after the 10-minute intervention and before the post-intervention running trial.

  2. Distal-Tibial Acceleration at Initial Contact

    Resultant distal-tibial acceleration was measured using bilateral inertial measurement units and expressed in meters per second squared (m/s²). Values from 10 consecutive steps were averaged for each limb, and the left- and right-limb means were subsequently averaged.

    Time frame: At initial contact during the post-intervention treadmill running trial; events were identified within the 60-120-second analysis interval.

  3. Distal-Tibial Angular Velocity at Initial Contact

    Resultant distal-tibial angular velocity was measured using bilateral inertial measurement units and expressed in degrees per second (°/s). Values from 10 consecutive steps were averaged for each limb, and the left- and right-limb means were subsequently averaged.

    Time frame: At initial contact during the post-intervention treadmill running trial; events were identified within the 60-120-second analysis interval.

  4. Distal-Tibial Angular Velocity at Toe-Off

    Resultant distal-tibial angular velocity was measured using bilateral inertial measurement units and expressed in degrees per second (°/s). Values from 10 consecutive steps were averaged for each limb, and the left- and right-limb means were subsequently averaged.

    Time frame: At toe-off during the post-intervention treadmill running trial; events were identified within the 60-120-second analysis interval.

  5. Distal-Tibial Acceleration at Toe-Off

    Resultant distal-tibial acceleration was measured using bilateral inertial measurement units and expressed in meters per second squared (m/s²). Values from 10 consecutive steps were averaged for each limb, and the left- and right-limb means were subsequently averaged.

    Time frame: At toe-off during the post-intervention treadmill running trial; events were identified within the 60-120-second analysis interval.

  6. Step Width During Running

    Step width was measured from posterior-view two-dimensional video analysis and expressed in centimeters. Ten consecutive steps were analyzed and averaged for each participant and condition.

    Time frame: During the 3-minute post-intervention treadmill running trial; 10 consecutive steps were analyzed from 60 to 120 seconds after the start of running.

  7. Sacral Acceleration at Initial Contact

    Resultant sacral acceleration was measured using an inertial measurement unit positioned over the S2 region and expressed in meters per second squared (m/s²). Values from 10 consecutive steps were averaged for each participant and condition.

    Time frame: At initial contact during the post-intervention treadmill running trial; events were identified within the 60-120-second analysis interval.

  8. Sacral Acceleration at Toe-Off

    Resultant sacral acceleration was measured using an inertial measurement unit positioned over the S2 region and expressed in meters per second squared (m/s²). Values from 10 consecutive steps were averaged for each participant and condition.

    Time frame: At toe-off during the post-intervention treadmill running trial; events were identified within the 60-120-second analysis interval.

  9. Sacral Angular Velocity at Initial Contact

    Resultant sacral angular velocity was measured using an inertial measurement unit positioned over the S2 region and expressed in degrees per second (°/s). Values from 10 consecutive steps were averaged for each participant and condition.

    Time frame: At initial contact during the post-intervention treadmill running trial; events were identified within the 60-120-second analysis interval.

  10. Sacral Angular Velocity at Toe-Off

    Resultant sacral angular velocity was measured using an inertial measurement unit positioned over the S2 region and expressed in degrees per second (°/s). Values from 10 consecutive steps were averaged for each participant and condition.

    Time frame: At toe-off during the post-intervention treadmill running trial; events were identified within the 60-120-second analysis interval.

Secondary outcomes

  1. Heart Rate at the End of the Intervention

    Heart rate was recorded using a Polar H10 chest-strap heart-rate monitor and averaged over the final 10 seconds of the 10-minute intervention. Heart rate was expressed in beats per minute (beats/min).

    Time frame: During the final 10 seconds of the 10-minute intervention.

  2. Sagittal Trunk Inclination Angle at Initial Contact

    Sagittal trunk inclination angle was measured from lateral-view two-dimensional video analysis and expressed in degrees. Positive values indicated trunk flexion and negative values indicated trunk extension. Ten consecutive steps were analyzed and averaged for each participant and condition.

    Time frame: At initial contact during the post-intervention treadmill running trial; 10 consecutive steps were analyzed from 60 to 120 seconds after the start of running.

  3. Sagittal Trunk Inclination Angle at Toe-Off

    Sagittal trunk inclination angle was measured from lateral-view two-dimensional video analysis and expressed in degrees. Positive values indicated trunk flexion and negative values indicated trunk extension. Ten consecutive steps were analyzed and averaged for each participant and condition.

    Time frame: At toe-off during the post-intervention treadmill running trial; 10 consecutive steps were analyzed from 60 to 120 seconds after the start of running.

  4. Knee-Flexion Angle at Initial Contact

    Knee-flexion angle was measured from lateral-view two-dimensional video analysis and expressed in degrees. Smaller values represented a more extended knee position. Ten consecutive steps were analyzed and averaged for each participant and condition.

    Time frame: At initial contact during the post-intervention treadmill running trial; 10 consecutive steps were analyzed from 60 to 120 seconds after the start of running.

  5. Knee-Flexion Angle at Toe-Off

    Knee-flexion angle was measured from lateral-view two-dimensional video analysis and expressed in degrees. Smaller values represented a more extended knee position. Ten consecutive steps were analyzed and averaged for each participant and condition.

    Time frame: At toe-off during the post-intervention treadmill running trial; 10 consecutive steps were analyzed from 60 to 120 seconds after the start of running.

07

Study locations

1 site
  • Chia Nan University of Pharmacy & Science
    Tainan, 717301, Taiwan
08

References and documents

Publications

  • do Nascimento AP, de Oliveira GA, Bressanin JPB, Aguirra P, Ribeiro AS, Caldeira LFS, Casonatto J, Ferraresi C, Aguiar AF. Acute dose-response effect of photobiomodulation therapy on 5-km running performance in trained runners: a randomized, double-blind, placebo-controlled, crossover study. Lasers Med Sci. 2024 May 31;39(1):145. doi: 10.1007/s10103-024-04099-8. PubMed 38819613 ↗
  • De Marchi T, Leal Junior EC, Bortoli C, Tomazoni SS, Lopes-Martins RA, Salvador M. Low-level laser therapy (LLLT) in human progressive-intensity running: effects on exercise performance, skeletal muscle status, and oxidative stress. Lasers Med Sci. 2012 Jan;27(1):231-6. doi: 10.1007/s10103-011-0955-5. Epub 2011 Jul 8. PubMed 21739259 ↗
  • de Brito Vieira WH, Bezerra RM, Queiroz RA, Maciel NF, Parizotto NA, Ferraresi C. Use of low-level laser therapy (808 nm) to muscle fatigue resistance: a randomized double-blind crossover trial. Photomed Laser Surg. 2014 Dec;32(12):678-85. doi: 10.1089/pho.2014.3812. PubMed 25496083 ↗
  • Vanin AA, Verhagen E, Barboza SD, Costa LOP, Leal-Junior ECP. Photobiomodulation therapy for the improvement of muscular performance and reduction of muscular fatigue associated with exercise in healthy people: a systematic review and meta-analysis. Lasers Med Sci. 2018 Jan;33(1):181-214. doi: 10.1007/s10103-017-2368-6. Epub 2017 Oct 31. PubMed 29090398 ↗
  • Zandbergen MA, Marotta L, Bulthuis R, Buurke JH, Veltink PH, Reenalda J. Effects of level running-induced fatigue on running kinematics: A systematic review and meta-analysis. Gait Posture. 2023 Jan;99:60-75. doi: 10.1016/j.gaitpost.2022.09.089. Epub 2022 Oct 12. PubMed 36332318 ↗

Individual participant data

Plan to share: No — Individual participant data will not be made publicly available because of participant privacy and ethical considerations. De-identified data may be available from the corresponding author upon reasonable request, subject to applicable ethical and institutional restrictions.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Feb 2025 to primary completion in Jun 2025, 4 months.

Of 936 non-industry interventional studies with no phase under Fatigue, half reached primary completion within 12 months of starting (the median), counting those still running; a quarter within 5 and three quarters within 27. This study's 4 months is below that.

Counting every sponsor, half of 989 studies reached it within 11 months; a quarter within 5 and three quarters within 27.

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

Registered
Sep 2, 2026
First posted
Sep 9, 2026
StartActual
Feb 17, 2025
Primary completionActual
Jun 19, 2025
CompletionActual
Jun 19, 2025
Last update
Sep 9, 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.
No changes since tracking began. The registry record was last updated on Sep 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07808814
Lead sponsor
Chia Nan University of Pharmacy & Science
Collaborators
Lasinmed Medical Electronics Co., Ltd.
Responsible party
Chen, Tsan-Yang (Assistant Professor, Chia Nan University of Pharmacy & Science) — Principal investigator
First posted
Sep 9, 2026
Start date
Feb 17, 2025
Primary completion
Jun 19, 2025
Completion
Jun 19, 2025
Last update
Sep 9, 2026

Oversight

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

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