RCT of Mind-body in Long COVID and Myalgic Encephalomyelitis

NCT ID
NCT06933173
Registry status
Recruiting
Study type
Not specified in the registry data
Phase
Not applicable
Sponsor
University of Alberta

Overview

ClinicalTrials.gov lists this study as Recruiting.

Enrollment: 200 participants (Estimated).

What is being studied

No interventions are listed in the registry data.

Who may be eligible

Ages
Not specified in the registry data
Sex
Not specified in the registry data
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: * Age 18 years or older; * Individuals diagnosed with ME/CFS, according to the Institute of Medicine (2015) criteria, for more than six months. Exclusion Criteria: Individuals who: 1) are too ill to participate; 2) lack reliable internet; 3) cannot communicate in English; 4) Presently have or ever had inflammatory bowel disease; and/or 5) Have been prescribed or used an oral or systemic (infusion) antibiotic in the past one month-;; 6) are participating in a concurrent study; 7) are participating in a concurrent mind-body intervention during the study period including * Art Therapy * Autogenic training * Biofeedback/neurofeedback * Breathing exercise * Cognitive restructuring * Dynamic Neural Retraining System * Emotional Freedom Techniques (EFT) * Eye movement desensitization and reprocessing (EMDR) * Guided imagery * Hypnotherapy/self-hypnosis * Meditation (mindfulness, mantra, guided, transcendental) * Mindfulness-based cognitive therapy (MBCT) * Mindfulness-based Stress Reduction (MBSR) * Music therapy * Neurolinguistic programming * Psychological flexibility * Qigong * Relaxation therapy (relaxation response, progressive muscle relaxation) * Tai Chi * Visualization * Yoga and/or starting any other new treatment during the study period, including any mind-body therapy, psychotherapy, prescription medication, over-the-counter medication, etc; 8) have any active medical condition (untreated/uncontrolled) that may explain the presence of fatigue including: * untreated hypothyroidism (including Hashimoto's disease) * hyperthyroidism * diabetes mellitus * iron deficiency anemia * other treatable anemia * iron overload syndrome * adrenal insufficiency * Cushing's syndrome * anorexia nervosa * iatrogenic conditions such as side effects or interactions of medication(s) or supplements • Rheumatological disorders: * rheumatoid arthritis * lupus * polymyositis * polymyalgia rheumatica * Sjogren's Syndrome * Ehlers Danlos Syndromes \[Hypermobility type\] • Other heritable disorders of connective tissue: * Marfan syndrome * Stickler syndrome etc. * Multiple sclerosis * Celiac disease * Note: Patients with celiac disease can present without gastrointestinal symptoms • Immune disorders * such as HIV/AIDS • Sleep disorders * including obstructive sleep apnea • Prior illnesses may relapse or may not have completely resolved during treatment. * Examples are certain malignancies * leukemia * infectious diseases such as tuberculosis and chronic hepatitis • Active primary psychiatric disorders * eating disorders * alcohol * substance use disorder

Study locations

2 study locations are listed.

Site recruitment status is not specified in the registry data for these locations.

Countries: Canada

  • Alberta, Canada: 2

Sample of listed locations

  • Peter Lougheed Hospital — Calgary, Alberta, Canada — Site recruitment status not specified in the registry data
  • University of Alberta Hospital/Kaye Edmonton Clinic — Edmonton, Alberta, Canada — Site recruitment status not specified in the registry data

Study details

Start date
July 10, 2025
Primary completion date
December 31, 2027
First posted
April 18, 2025

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT06933173
Registry last updated
September 9, 2026
QualifiedStudies registry data refreshed
September 21, 2026

View NCT06933173 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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