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NCT Number: NCT07546539

Photobiomodulation in Chronic Fatigue Syndrome

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)

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The larkana General hospital , larkana

Larkana, Sindh, Pakistan

Location status: Recruiting

Location contact

ADIL AMIR ALI

PRINCIPAL_INVESTIGATOR

Dr Naseebullah

CONTACT

[email protected]

923337201393

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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 -

Treatment and study plan

Photobiomodulation (Low-Level Laser Therapy)

Device

Low-level laser therapy will be delivered using a Class 3B laser device (808 nm wavelength, 100 mW power output). The laser will be applied in contact mode using a static technique perpendicular to the skin surface.

Treatment will target bilateral muscle groups: upper trapezius, biceps brachii, posterior deltoid, lumbar paraspinals, gluteus maximus, and vastus lateralis. Each muscle will receive irradiation at 16 points spaced 1 cm apart, delivering 4 Joules per point (total 64 Joules per muscle).

Sessions will be conducted three times per week for 8 weeks (total 24 sessions).

sham Photobiomodulation (LLLT)

Device

Sham laser therapy will be administered using the same device without emission of therapeutic laser energy. The device will appear active and will be applied with identical procedures, duration, and frequency as the active treatment to ensure participant blinding.

Primary outcomes

  1. Fatigue Improvement

    Time frame: Baseline to Week 8-12 (end of intervention)

    Fatigue will be assessed using validated self-reported instruments to evaluate the effect of photobiomodulation therapy on chronic fatigue symptoms.

    The Fatigue Severity Scale (Fatigue Severity Scale) is a 9-item questionnaire that measures the impact of fatigue on daily functioning. Each item is scored on a 7-point Likert scale, and the final score is calculated as the mean of all items, with higher scores indicating greater fatigue severity.

    The Multidimensional Fatigue Inventory (Multidimensional Fatigue Inventory) is a 20-item instrument assessing five dimensions: general fatigue, physical fatigue, mental fatigue, reduced activity, and reduced motivation. Each domain is scored on a 5-point Likert scale, with higher scores indicating increased fatigue.

Secondary outcomes

  1. Health Related Quality of Life

    Time frame: Baseline to Week 8-12

    Quality of life will be assessed using either the Medical Outcomes Study 36-Item Short Form Health Survey (Short Form-36 Health Survey) or the World Health Organization Quality of Life Brief Version (World Health Organization Quality of Life-BREF).

    The Short Form-36 Health Survey evaluates eight domains including physical functioning, bodily pain, vitality, and mental health. Scores range from 0 to 100, with higher scores indicating better quality of life.

    The World Health Organization Quality of Life-BREF consists of 26 items covering physical, psychological, social, and environmental domains, with higher scores indicating better perceived quality of life.

  2. Functional Capacity

    Time frame: Baseline to Week 8-12 (end of intervention)

    Functional capacity will be assessed using the Six-Minute Walk Test (Six-Minute Walk Test). This test measures the total distance (in meters) a participant can walk in six minutes on a flat surface and reflects submaximal aerobic capacity and endurance.

  3. Pain Intensity

    Time frame: Baseline to Week 8-12

    Pain intensity will be measured using the Visual Analog Scale (Visual Analog Scale), a 10-centimeter horizontal line ranging from "no pain" to "worst imaginable pain." Scores are recorded in centimeters, with higher scores indicating greater pain intensity.

  4. Sleep Quality

    Time frame: Baseline to Week 8-12

    Sleep quality will be evaluated using the Pittsburgh Sleep Quality Index (Pittsburgh Sleep Quality Index). This 19-item questionnaire assesses sleep quality over the past month across seven components. Global scores range from 0 to 21, with higher scores indicating poorer sleep quality.

  5. Psychological Well-Being

    Time frame: Baseline to Week 8-12

    Psychological well-being will be assessed using either the Hospital Anxiety and Depression Scale (Hospital Anxiety and Depression Scale) or the Beck Depression Inventory (Beck Depression Inventory).

    The Hospital Anxiety and Depression Scale includes 14 items divided into anxiety and depression subscales, each scored from 0 to 21.

    The Beck Depression Inventory is a 21-item self-report questionnaire with scores ranging from 0 to 63, where higher scores indicate more severe depressive symptoms.

  6. Sustained Effects

    Time frame: Week 16 and Week 24 follow-up

    Follow-up assessments will be conducted to determine whether improvements in fatigue, pain, and functional capacity are sustained after completion of the intervention.

  7. Safety and Tolerability

    Time frame: Throughout Week 8-12 intervention period

    Safety and tolerability will be assessed by monitoring participant-reported discomfort, skin irritation, or other minor side effects occurring during or after Photobiomodulation therapy sessions.

  8. Adverse Effects and Safety Profile

    Time frame: From baseline through Week 24 (study completion)

    All adverse events will be recorded and categorized by type, severity, duration, and relationship to the intervention. Serious adverse events will be reported immediately in accordance with regulatory requirements.

Study contacts

Contact information is provided by the study sponsor or research team.

Dr Adil Amir Ali Dr Aadil Amir Ali, PhD

CONTACT

[email protected]

923002929464

Sponsors and collaborators

Lead sponsor

University of Lahore

Other

Registry information

Official study title

The Role of Photobiomodulation in Patients With Chronic Fatigue Syndrome

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Apr 22, 2026
Registry last updated
Jun 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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