The Effects of Energy Healing in Fibromyalgia

A vizsgálat adatai

Ki végzi

University of California, Irvine

Azonosító

NCT06552728

A regiszteradat frissítve

2026. november 10.

Eredeti leírás

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.A teljes eredeti leírásKevesebb

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.

Bevonási feltételek: Female; 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.

Kizáró feltételek: 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 a concurrent autoimmune or inflammatory disease such as rheumatoid arthritis, systemic lupus erythematosus, inflammatory bowel disease, etc. that causes pain; 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; 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; Routine daily use of narcotic analgesics or history of substance abuse; 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; 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; EH within the last 6-months; Presence of known past procedures, devices in the body, claustrophobia, or other contraindications for MRI; Peripheral neuropathy that interferes with activities of daily living; Pregnant or nursing; Current active litigation for FM pain.

ClinicalTrials.gov NCT06552728