Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06933173

RCT of Mind-body in Long COVID and Myalgic Encephalomyelitis

Led by University of Alberta · Updated on 2026-05-07

200

Participants Needed

3

Research Sites

137 weeks

Total Duration

On this page

Sponsors

U

University of Alberta

Lead Sponsor

C

College of Physicians and Surgeons of Alberta

Collaborating Sponsor

AI-Summary

What this Trial Is About

We are studying the effect of a mind-body treatment for people with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) with or without Long COVID (LC). Our team recognizes that ME/CFS and Long COVID are serious, debilitating, biomedical conditions. ME/CFS can affect many different parts of the body, such as the nervous system, immune system, and metabolism. It is hypothesized that central sensitization (i.e., when nerves get too excited) may influence these complex conditions and may make symptoms worse. This study explores a mind-body program called the Dynamic Neural Retraining System™, or DNRS™. Mind-body interventions (MBIs) focus on how the brain, mind, body, and behaviour interact to improve health and well-being. These techniques help people become more aware of themselves, take better care of their health, and boost mood, quality of life, and coping skills. MBIs use the brain's ability to change (neuroplasticity) by reinforcing certain thoughts, feelings, or behaviours that support changes in biology and function. MBIs may influence physical health by affecting how the brain and body communicate through chemicals such as hormones and neurotransmitters. Objective fMRI evidence shows that practising MBIs can change brain structure and function. This makes MBIs a potential good fit for people with chronic illnesses like ME/CFS and LC, which involve complex interactions between the brain, immune system, and hormones. There is no rigorous peer-reviewed evidence that DNRS is effective. Our study will address this question using subjective and objective measurements in a multiple-methods wait-list randomized controlled trial. The objectives of this study are to: 1) examine the effectiveness of the DNRS program for individuals diagnosed with ME/CFS with and without Long COVID, compared to a treatment-as-usual wait-list control group on a range of patient-reported outcomes including health-related quality of life, fatigue, pain, anxiety and depression and objective measures including daily steps, heart rate variability, and sleep; 2) quantify metabolic changes through untargeted serum metabolomics profiling, 3) determine if metabolomics screening can predict treatment responsiveness to DNRS; and 4) identify the microbial signatures of large bowel microbiota in Long COVID patients pre and post MBI. A descriptive qualitative study will also be conducted in a sample of participants to learn more about their experiences during the trial.

CONDITIONS

Official Title

RCT of Mind-body in Long COVID and Myalgic Encephalomyelitis

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Diagnosed with ME/CFS according to the Institute of Medicine (2015) criteria for more than six months
Not Eligible

You will not qualify if you...

  • Too ill to participate
  • Lack reliable internet access
  • Cannot communicate in English
  • Have or have had inflammatory bowel disease
  • Used oral or systemic antibiotics in the past month
  • Participating in another study
  • Participating in any concurrent mind-body intervention or starting new treatments during the study
  • Have untreated or uncontrolled medical conditions that may cause fatigue, such as thyroid disorders, diabetes, anemia, adrenal or adrenal-related disorders, anorexia nervosa, medication side effects
  • Have rheumatological disorders like rheumatoid arthritis, lupus, polymyositis, polymyalgia rheumatica, Sjogren's Syndrome, or Ehlers Danlos Syndromes (Hypermobility type)
  • Have other heritable connective tissue disorders such as Marfan syndrome or Stickler syndrome
  • Have multiple sclerosis
  • Have celiac disease
  • Have immune disorders such as HIV/AIDS
  • Have sleep disorders including obstructive sleep apnea
  • Have active or unresolved prior illnesses like certain malignancies, leukemia, tuberculosis, or chronic hepatitis
  • Have active primary psychiatric disorders including eating disorders, alcohol or substance use disorders

AI-Screening

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Trial Site Locations

Total: 3 locations

1

Peter Lougheed Hospital

Calgary, Alberta, Canada

Actively Recruiting

2

University of Alberta Hospital/Kaye Edmonton Clinic

Edmonton, Alberta, Canada

Actively Recruiting

3

Women's College Hospital

Toronto, Ontario, Canada

Actively Recruiting

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Research Team

M

MILES RCT team

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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