Chronic Pain Clinical Trial
Official title:
Feasibility of Using Holographic Memory Resolution® (HMR) in Patients/Clients With Pain
NCT number | NCT05001399 |
Other study ID # | 21.012 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | October 25, 2021 |
Est. completion date | July 18, 2022 |
Verified date | October 2022 |
Source | Billings Clinic |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Study Purpose: This study will explore the feasibility of administering Holographic Memory Resolution® (HMR) to adults who are experiencing chronic pain for 6 months or more.
Status | Completed |
Enrollment | 60 |
Est. completion date | July 18, 2022 |
Est. primary completion date | June 29, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Patient age 18 years or older - Suffering from pain of 4 or greater intensity on a 0-10 scale with "0" being no pain and "10" being worst possible pain. - Pain symptoms will have been present for at least 6 months. Patients with chronic migraine headaches will be eligible if headaches occur at least every two months. - Associated symptoms could include anxiety, depression, or physical symptoms such as pain, migraines, or other symptoms that have interfered with quality of life or work/life balance. - Interested clients will have primary care provider agreement to participate in the study. Exclusion Criteria: - Diagnosis of psychosis or schizoaffective disorder, personality disorder, or suicidal ideation. - Clients taking mood altering substances and those that have a propensity toward altering delta, theta, alpha, and beta wave ranges will be excluded. These substances include but are not limited to Cannabis/Marijuana/ hashish/THC, PCP, phencyclidine, or Angel dust, Barbiturates, Benzodiazepines, Opioids/heroin, Clozapine (+++delta/slow waves/- - alpha waves), Lithium, Stimulants/ (Illicit: Cocaine, Methamphetamine), and Hallucinogens/MDMA (ecstasy)/LSD. - Clients who ingest alcohol must be 3 months abstinent/in recovery before session if alcohol dependent and 48 hours abstinent before session if not alcohol dependent/in recovery. |
Country | Name | City | State |
---|---|---|---|
United States | Billings Clinic | Billings | Montana |
United States | Healing Dimensions ACC | Tucson | Arizona |
Lead Sponsor | Collaborator |
---|---|
Billings Clinic | Healing Dimensions, ACC |
United States,
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* Note: There are 18 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Completion Rate of an HMR Intervention | The percentage of patients who complete 4 HMR sessions. | Following 4 HMR sessions, approximately 8-9 weeks per participant. | |
Secondary | Somatic Symptomatic Scale (SSS-8) | The SSS-8, an abbreviated version of the PHQ-15, is a validated 8-item client-report measure of somatic symptom burden. Respondents are asked to answer the question "During the past 7 days, how much have you been bothered by any of the following problems?" concerning gastrointestinal, pain, fatigue, and cardiopulmonary aspects. Items are scored on a 5-point Likert scale (0=Not at all, 1=A little bit, 2=Somewhat, 3=Quite a bit, 4=Very much). Somatic symptom scoring ranges from 0-32 [(no to minimal (0-3 points), low (4-7 points), medium (8-11 points), high (12-15 points), and very high (16-32 points)]. | Baseline, prior to Session 3 ( Day 14-24), prior to Session 4 (8-9 weeks), and 1 month after Session 4. |
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