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Recruiting EARLY_Phase 1 NCT06472622

NCT06472622 Functional Neuroimaging to Detect the Neural Signatures of the Unpleasantness of Pain and Effort

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Clinical Trial Summary
NCT ID NCT06472622
Status Recruiting
Phase EARLY_Phase 1
Sponsor National Institute of Neurological Disorders and Stroke (NINDS)
Condition Fatigue Syndrome, Chronic
Study Type INTERVENTIONAL
Enrollment 47 participants
Start Date 2025-04-09
Primary Completion 2034-06-30

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 50 Years
Study Type INTERVENTIONAL
Interventions
Thermal Pain StimulationPhysical Effort Stimulation

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

Phase 1 is the earliest stage of human testing — safety and dosage are the primary focus. Visits are frequent and medical supervision is intensive. You will be among the first people to receive this treatment.

This trial targets 47 participants in total. It began in 2025-04-09 with a primary completion date of 2034-06-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Background: The way the brain processes rewards and punishments may play a role in some disorders of the nervous system. People with chronic overlapping pain conditions (such as myalgic encephalomyelitis/chronic fatigue syndrome \[ME/CFS\]) may have heightened responses to unpleasant, punishing sensations. Some of these conditions may also cause heightened responses to effort; this is an unpleasant sensation felt during physical and mental exertion. Objective: To learn more about how the brain processes different unpleasant sensations. Eligibility: People aged 18 to 50 years with ME/CFS. Healthy volunteers are also needed. Design: Participants will have 3 visits in 1 to 5 weeks. Visit 1: Participants may have a neurologic exam. They will have a mock magnetic resonance imaging (MRI) scan. They will lie on a bed in a wooden tube while they practice 2 tasks: Thermal pain rating: A device that creates mild to moderate heat will be placed on one leg. Physical effort rating: Participants will squeeze a plastic bar with different levels of force. Visit 2: Participants will have a real MRI scan. They will lie on a table that slides into a large tube. Visit 3: Participants will have another MRI scan. They will repeat the thermal pain and physical effort tasks while in the scanner. Sensors will be placed on 1 arm to measure how the muscles function as they squeeze the bar. Their heart rate will be tested: They will hold their finger against a camera lens for 1 minute. They will do 2 other tasks: 1 requires repeatedly pressing a key on a keyboard, and the other requires squeezing a bar.

Eligibility Criteria

* INCLUSION CRITERIA: Healthy Controls: In order to be eligible to participate in this study as a healthy control, an individual must meet all the following criteria: 1. Ability of subject to understand and the willingness to sign a written informed consent document. 2. Stated willingness to comply with all study procedures and availability for the duration of the study. 3. Male or female, aged 18-50 (inclusive). 4. Good general health as evidenced by medical history and/or physical examination. ME/CFS Patients: In order to be eligible to participate in this study as an ME/CFS patient, an individual must meet all the following criteria: 1. Ability of subject to understand and the willingness to sign a written informed consent document. 2. Stated willingness to comply with all study procedures and availability for the duration of the study. 3. Male or female, aged 18-50 (inclusive). 4. Has a diagnosis of ME/CFS, meeting at least one of three ME/CFS criteria: the 1994 Fukuda Criteria, the 2003 Canadian Consensus Criteria for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome, or the Institute of Medicine Diagnostic Criteria. EXCLUSION CRITERIA: Healthy Controls: 1. Any current major neurological or psychiatric disorder such as (but not limited to) stroke, Parkinson s disease, Alzheimer s disease, schizophrenia, or major depressive disorder. 2. Any other current major medical disorder, such as a kidney disease, liver disease, cardiovascular disease, chronic pain condition, or any other disorder which, in the opinion of the PI would make participation risky for the individual or negatively affect the individual s ability to cooperate with study procedures. 3. Current use of medications acting primarily on the central nervous system, such as antidepressants, stimulants, etc. 4. Use of opioid medications for more than two weeks within the last two years or any use in the last month. 5. Current or history of substance use disorder, binge drinking, illegal drug use, or excessive tobacco use (defined as more than 10 cigarettes of nicotine per week). 6. Any more than occasional use of cannabis, defined as a score \>1 (indicating use on more than one or two days in the last two weeks) on the marijuana use item of the DSM-5 Level 2-Substance Use-Adult questionnaire. 7. Any use of other illicit drugs or misuse of prescription medications, defined as a score \>0 on any of the other items of the DSM-5 Level 2-Substance Use-Adult questionnaire. 8. Condition or injury affecting grip. 9. Condition or injury affecting extremities that would alter peripheral sensitivity to painful thermal stimuli or would otherwise cause such stimuli to be contraindicated. 10. Contraindications to MRI, including ferromagnetic metal in the cranial cavity or eye, implanted neural stimulator, cochlear implant, or ocular foreign body, implanted cardiac pacemaker, auto-defibrillator, or pump, non-removable body piercing, claustrophobia, inability to lie supine for 90 minutes, known pregnancy, or plans to become pregnant during the study. 11. Members of the NINDS BNU and their family members. 12. Non-English speakers will be excluded from the study as several study instruments do not have validated translations. ME/CFS Patients: 1. Any current major neurological or psychiatric disorder, other than ME/CFS, such as (but not limited to) stroke, Parkinson s disease, Alzheimer s disease, schizophrenia, or major depressive disorder. 2. Any other current major medical disorder, other than ME/CFS, such as a kidney disease, liver disease, cardiovascular disease, chronic pain condition, or any other disorder which, in the opinion of the PI would make participation risky for the individual or negatively affect the individual s ability to cooperate with study procedures. 3. Current use of psychomotor stimulants, antipsychotics, or benzodiazepines. 4. Use of opioid medications for more than two weeks within the last two years or any use in the last month. 5. Current or history of substance use disorder, binge drinking, illegal drug use, or excessive tobacco use (defined as more than 10 cigarettes of nicotine per week). 6. Any more than occasional use of cannabis, defined as a score \>1 (indicating use on more than one or two days in the last two weeks) on the marijuana use item of the DSM-5 Level 2-Substance Use-Adult questionnaire. 7. Any use of other illicit drugs or misuse of prescription medications, defined as a score \>0 on any of the other items of the DSM-5 Level 2-Substance Use-Adult questionnaire. 8. Condition or injury affecting grip. 9. Condition or injury affecting extremities that would alter peripheral sensitivity to painful thermal stimuli or would otherwise cause such stimuli to be contraindicated. 10. Contraindications to MRI, including ferromagnetic metal in the cranial cavity or eye, implanted neural stimulator, cochlear implant, or ocular foreign body, implanted cardiac pacemaker, auto-defibrillator, or pump, non-removable body piercing, claustrophobia, inability to lie supine for 90 minutes, known pregnancy, or plans to become pregnant during the study. 11. Members of the NINDS BNU and their family members. 12. Non-English speakers will be excluded from the study as several study instruments do not have validated translations.

Contact & Investigator

Central Contact

Nicholas J Madian, Ph.D.

✉ nicholas.madian@nih.gov

📞 (301) 480-9787

Principal Investigator

Eric M Wassermann, M.D.

PRINCIPAL INVESTIGATOR

National Institute of Neurological Disorders and Stroke (NINDS)

Frequently Asked Questions

Who can join the NCT06472622 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 50 Years, studying Fatigue Syndrome, Chronic. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT06472622 trial and what does that mean for participants?

Phase 1 trials are the first stage of human testing. The primary goal is to assess safety and determine appropriate dosage levels. Participants are closely monitored. These trials typically involve a small number of volunteers.

Is NCT06472622 currently recruiting?

Yes, NCT06472622 is actively recruiting participants. Contact the research team at nicholas.madian@nih.gov for enrollment information.

Where is the NCT06472622 trial being conducted?

This trial is being conducted at Bethesda, United States.

Who is sponsoring the NCT06472622 clinical trial?

NCT06472622 is sponsored by National Institute of Neurological Disorders and Stroke (NINDS). The principal investigator is Eric M Wassermann, M.D. at National Institute of Neurological Disorders and Stroke (NINDS). The trial plans to enroll 47 participants.

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