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Feasibility of Using Holographic Memory Resolution® (HMR) in Patients/Clients With Pain
NCT05001399 · View on ClinicalTrials.gov ↗
Study Summary
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.
Conditions Studied
Interventions
- BEHAVIORAL Holographic Memory Resolution® (HMR)
Study Locations (2)
Arizona
- Healing Dimensions ACC — Tucson
Montana
- Billings Clinic — Billings
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2021-10-25 |
| Est. Completion | 2022-07-18 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05001399
The ClinicalTrials.gov registry entry for NCT05001399 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Billings Clinic, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with Chronic Pain appearing as the primary indexed condition, and to 1 intervention — of which Holographic Memory Resolution® (HMR) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT05001399 reports 2 study locations spanning 2 distinct geographic areas — top geographies include Arizona, Montana. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT05001399 about?
NCT05001399 is a clinical study titled "Feasibility of Using Holographic Memory Resolution® (HMR) in Patients/Clients With Pain". 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.
What is the current status of trial NCT05001399?
This trial is currently completed. It is a NA study. The enrollment target is 60 participants. The study started on 2021-10-25. Estimated completion is 2022-07-18.
What conditions does trial NCT05001399 study?
This clinical trial studies the following conditions: Chronic Pain, Stress Disorders, Post-Traumatic, Headache, Migraine. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05001399?
The interventions under investigation include: Holographic Memory Resolution® (HMR) (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05001399?
This trial is sponsored by Billings Clinic, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05001399 being conducted?
This trial has 2 study locations across Arizona, Montana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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