Actively Recruiting

Phase Not Applicable
Age: 18Years - 35Years
All Genders
Healthy Volunteers
ID07422272

Examining the Immediate Effects of Low-Level Laser Therapy on Pain Threshold and Tolerance in Healthy Adults: A Randomized Controlled Trial

Led by European University of Lefke · Updated on 2026-02-19

52

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Pain is described as an unpleasant sensory and emotional experience linked to actual or potential tissue damage. This research evaluates whether a single session of Low-Level Laser Therapy (LLLT), a safe and noninvasive treatment with pain-relief and anti-inflammatory effects, can produce immediate changes in pain threshold and pain tolerance in healthy adults. This study focuses on acute nociceptive pain, common in musculoskeletal conditions, and aims to understand LLLT's immediate impact compared to a sham treatment. Participants will be randomly assigned to receive either active LLLT or a sham laser procedure. The active treatment uses a 904 nm wavelength laser applied to three points near the medial epicondyle for a total of 6 minutes, delivering a set energy dose. The sham group undergoes the same procedure without actual laser emission to control for placebo effects. Both groups and the researcher wear safety eyewear during the process. During the study, researchers will measure electrical pain threshold and pain tolerance before and immediately after the intervention. Participants are healthy adults aged 18 to 35 without chronic medical conditions or pain. The trial includes monitoring for safety and adherence to protocols. The total participation involves a single session assessing immediate effects, with no long-term follow-up described.

CONDITIONS

Brief Title

Acute Effects of LLLT on Pain Threshold and Pain Tolerance

Who Can Participate

Age: 18Years - 35Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 35 years
  • Healthy individuals without chronic medical conditions
  • Free from chronic or acute pain
  • All genders
  • Able to provide informed consent
Not Eligible

You will not qualify if you...

  • Menstruation at the time of testing
  • Sensory deficits (failure to pass sharp-dull test)
  • Pregnancy
  • History of epilepsy
  • Presence of cardiovascular conditions (including pacemaker)
  • Acute hand injuries
  • Diagnosed neurological disorders
  • Use of analgesics or NSAIDs within the previous 48 hours
  • Contraindications to low-level laser therapy or electrical stimulation (e.g., light sensitivity, malignancy)

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person) to assess eligibility criteria including health status and absence of contraindications.

Implementation

Duration - Single session

Participants receive either active Low-Level Laser Therapy (LLLT) or a sham procedure applied to three standardized points near the medial epicondyle. The laser or sham is applied for a total of 6 minutes while wearing safety eyewear.

1 visit (in-person) for laser or sham application and immediate assessments.

Trial Site Locations

Total: 1 location

1

European University of Lefke

Lefka, Northern Cyprus, Cyprus, 99780

Actively Recruiting

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Research Team

Y

Yara Mabrouk Houtar

A

Asst. Prof. Dr. Beraat Alptuğ Alptuğ

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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Published Research Related To This Trial

A systematic review and network meta-analysis on the optimal wavelength of low-level light therapy (LLLT) in treating knee osteoarthritis symptoms.

Tianxiang Fan, Yang Li, Arnold Y L Wong...

https://pubmed.ncbi.nlm.nih.gov/39367994

Efficacy of low-level laser therapy in the management of neck pain: a systematic review and meta-analysis of randomised placebo or active-treatment controlled trials.

Roberta T Chow, Mark I Johnson, Rodrigo A B Lopes-Martins...

https://pubmed.ncbi.nlm.nih.gov/19913903