RCT of Mind-body in Long COVID and Myalgic Encephalomyelitis

NCT ID: NCT06933173

Last Updated: 2025-07-16

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 200 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-07-10
• Study Completion Date: 2027-03-31

Brief Summary

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

Myalgic Encephalomyelitis/Chronic Fatigue Syndrome

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

DNRS intervention group

Group Type: EXPERIMENTAL

Dynamic neural retraining system

Intervention Type: OTHER

Description: The DNRS program includes the following components: 1) cognitive-behavioural therapy; 2) mindfulness-based cognitive restructuring; 3) emotional restructuring therapy; 4) neural linguistic programming; 5) incremental training; and 6) behaviour modification therapy. DNRS offered in this study includes a 14-hour online course followed by a 12-week online "LIVING DNRS" group support program. The 14-hour online course includes a variety of exercises, instructional videos, and a workbook. Upon completion, participants are offered a 12-week LIVING DNRS Group Support program which provides individuals with support in how to best implement DNRS into their daily lives with the help of a trained facilitator as well as peer support.

Wait-list control group

The waitlist control group will complete the experimental intervention after 4 months. During the waiting period, they will continue to receive usual care and will be asked to not participate in any other new treatments.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Dynamic neural retraining system

Description: The DNRS program includes the following components: 1) cognitive-behavioural therapy; 2) mindfulness-based cognitive restructuring; 3) emotional restructuring therapy; 4) neural linguistic programming; 5) incremental training; and 6) behaviour modification therapy. DNRS offered in this study includes a 14-hour online course followed by a 12-week online "LIVING DNRS" group support program. The 14-hour online course includes a variety of exercises, instructional videos, and a workbook. Upon completion, participants are offered a 12-week LIVING DNRS Group Support program which provides individuals with support in how to best implement DNRS into their daily lives with the help of a trained facilitator as well as peer support.

Intervention Type: OTHER

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

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

College of Physicians and Surgeons of Alberta

UNKNOWN

Sponsor Role: collaborator

University of Alberta

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Sunita Vohra, MD MSc FRCPC FCAHS

Role: PRINCIPAL_INVESTIGATOR

University of Alberta

Eleanor Stein, MD FRCPC

Role: PRINCIPAL_INVESTIGATOR

University of Calgary

Locations

Peter Lougheed Hospital

Calgary, Alberta, Canada

Site Status: RECRUITING

University of Alberta Hospital/Kaye Edmonton Clinic

Edmonton, Alberta, Canada

Site Status: RECRUITING

Women's College Hospital

Toronto, Ontario, Canada

Site Status: RECRUITING

Countries

Canada

Central Contacts

MILES RCT team

Role: CONTACT

rctmiles@ualberta.ca

780-680-8907

Facility Contacts

Elizabeth MacKay, MD

Role: primary

Elizabeth.Mackay@albertahealthservices.ca

MILES RCT team

Role: primary

rctmiles@ualberta.xa

780-680-8907

Sunita Vohra

Role: backup

svohra@ualberta.ca

Riina Bray

Role: primary

riina.bray@wchospital.ca

Other Identifiers

Pro00138185

Identifier Type: -

Identifier Source: org_study_id