Irvine, CANCT06552728Now EnrollingIRB Ready

Fibromyalgia Clinical Trial in Irvine, CA

Access cutting-edge fibromyalgia treatment through this clinical trial at a research site in Irvine. Study-provided care at no cost to qualified participants.

Sponsored by University of California, Irvine

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Expert Care in Irvine

Access fibromyalgia specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related fibromyalgia treatment provided free

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Check if you qualify for this fibromyalgia clinical trial in Irvine, CA

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Irvine

    Convenient for CA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Irvine site if eligible
  4. 4Begin participation

About This Fibromyalgia Study in Irvine

This study aims to study the clinical effects of Energy Healing using fMRI and determine its application to Fibromyalgia patients. We also want to find out how active Energy Healing compares to sham Energy Healing in terms of brain connectivity and pain interference scores.

Sponsor: University of California, Irvine

Who Can Participate

Inclusion Criteria

Over 18 and under 75 years of age.
Fibromyalgia patients must meet the 2016 Fibromyalgia Diagnostic Criteria for the classification of FM.
Mean recalled pain over the last seven days (7-day recall) between 4-10 cm on Visual - - - - Analog Scale (VAS) for pain with no pain free days in the last 2 months and active pain in resting state lying on back.
No contraindications for MRI, such as metal in the body or electrical devices in the body.
Willing to limit the introduction of any new medications or treatment modalities for control of FM symptoms during the study.
Able to travel to the study site to receive MRI, EH, and sham EH sessions up to twice weekly.
Understanding and willing to complete all study procedures.
Capable of giving written informed consent.
Proficient ability to speak, read, and write in english.

Exclusion Criteria

EH within the last 6-months.
Have received past treatment from Charlie Goldsmith or know of him or his work.
Contraindications to MRI and fcMRI methods. These may include but are not limited to: surgical clips, surgical staples, metal implants, and certain metallic dental material, claustrophobia, etc. \[Note: a more formal description of contraindications for MRI is present -in our DSM Plan\].
Presence of known past procedures, devices in the body, claustrophobia, or other contraindications for MRI
Presence of a concurrent autoimmune or inflammatory disease such as rheumatoid arthritis, systemic lupus erythematosus, inflammatory bowel disease, etc. that causes pain.
Peripheral neuropathy that interferes with activities of daily living.
Routine daily use of narcotic analgesics or history of substance abuse.
Stimulant medications, such as those used to treat ADD/ADHD (e.g., amphetamine/ dextroamphetamine \[Adderall®\], methylphenidate, dextroamphetamine), or the fatigue associated with sleep apnea or shift work (e.g., modafinil), are excluded.
Concurrent participation in other therapeutic trials.
Pregnant or nursing.
Severe psychiatric illnesses (current schizophrenia, major depression with suicidal ideation).
Active substance abuse disorder in the past 24 months as determined by subject self-report.
Use of PRN over the counter (OTC) pain medications (NSAIDs, etc.) on day of MRI scan.
Use of PRN narcotic pain medication 48 hours prior to MRI scan.
Current active litigation for FM pain.
Any impairment, activity or situation that in the judgment of the Principal Investigator or other team member that would prevent satisfactory completion of the study protocol. This includes unreliable, or inconsistent pain scores as deemed by the principal investigator.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Irvine?

Yes, this clinical trial (NCT06552728) has an active research site in Irvine, CA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Fibromyalgia Treatment Options in Irvine, CA

If you're searching for fibromyalgia treatment options in Irvine, CA, this clinical trial (NCT06552728) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Irvine research site is actively enrolling participants for this clinical trial. You'll receive care from experienced fibromyalgia specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all fibromyalgia clinical trials near you to find additional studies recruiting in your area.

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