Photobiomodulation in Chronic Fatigue Syndrome
Recruiting now · Not applicable · Has a placebo group
Conditions studied: Chronic Fatigue Syndrome (CFS), Quality of Life
In brief
The goal of this clinical trial is to evaluate whether photobiomodulation therapy (low-level laser therapy) can reduce fatigue and improve quality of life in patients with chronic fatigue syndrome (CFS). The study will include adults aged 18-60 years diagnosed with chronic fatigue syndrome. The main questions it aims to answer are: Does photobiomodulation therapy significantly reduce fatigue levels as measured by the Fatigue Severity Scale (FSS) and Multidimensional Fatigue Inventory (MFI-20)? Does photobiomodulation therapy improve pain, functional capacity, sleep quality, and psychological well-being in patients with chronic fatigue syndrome? Researchers will compare the low-level laser therapy group with a placebo (sham laser) group to determine whether photobiomodulation therapy leads to greater improvements in fatigue, pain, and overall quality of life. Participants will: Receive either active low-level laser therapy or placebo treatment three times per week for eight weeks Undergo assessments of fatigue, pain, functional capacity, quality of life, sleep quality, and psychological well-being at baseline and follow-up intervals (3, 6, and 12 months)
Key facts
- Study ID
- NCT07546539
- Run by
- University of Lahore
- People needed
- 40
- Starts
- 2026-06-15
- Expected to finish
- 2026-09-01
- Last updated by the study team
- 2026-06-24
Who can join
Age: 18 and older, up to 60. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age 18-60 years
- Diagnosis of a CFS according to the 2015 Institute of Medicine criteria
- Fatigue Severity Scale (FSS) score ≥ 4
- Ability to understand study procedures and provide informed consent
You may not qualify if…
- Comorbid psychiatric conditions (e.g., major depression, schizophrenia)
- Current use of corticosteroids or immunomodulators
- Known photosensitivity or dermatologic contraindications to LLLT
- Participation in structured exercise programs more than twice weekly
- Diagnosed malignancy or active infection -Not willing to be the part of study -
Where it is running
- The larkana General hospital , larkana — Larkana, Sindh, Pakistan (enrolling)
Full record on ClinicalTrials.gov
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