Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06050083 · ClinicalTrials.gov registry record · NA

Digital Clinical Hypnosis for Chronic Pain Management

A NA study, sponsored by University of Washington.

Completed
Registry status
NA
Development phase
100
Enrollment target

NCT06050083: Completed NA study, sponsored by University of Washington.

NCT06050083 is a NA study that has completed, run by University of Washington. The registered enrollment target is 100 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06050083, a NA study, has completed, sponsored by University of Washington.

COMPLETED
Registry status
NA
Development phase
100 participants
Enrollment target

Study Summary

This ClinicalTrials.gov posting contains two randomized controlled trials. The study procedures were identical, except Study 1 was funded by NIH and enrolled adults with chronic low back pain, whereas Study 2 was funded by the UW Department of Rehabilitation Medicine and enrolled adults with any type of chronic pain. Study 1 and 2 each enrolled 50 adults (N = 100 total across the two studies). Although Study 2 did not use NIH funds, we are including the results here because the studies were conducted simultaneously by the same PI (Dr. Jensen) with the same study procedures. Participants enrolled in the studies for a duration of 8 weeks. The studies test the feasibility and efficacy of a therapeutic hypnosis digital application (website), called Rose. The investigators wanted to determine if the Rose application was user-friendly and effective at improving quality of life and reducing pain for adults with chronic pain. If successfuly, the investigators hope to develop the Rose application into a mobile app that will be publicly available and managed by HypnoScientific Inc., a company that is co-owned by the investigators. Participants completed brief (15-20min) self-report surveys that ask about pain and mental health at three timepoints: Baseline (week 0), 4 weeks, and 8 weeks.

Primary Outcome

Total # of hypnosis sessions listened to by participants

Interventions

  • BEHAVIORAL Hypnosis audio recordings

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2024-01-04
Est. Completion 2024-09-15
Phase NA
University of Washington

1,048 total trials

What the finished NCT06050083 record still lists

NCT06050083 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower).

The record links to 0 conditions, and to 1 intervention - of which Hypnosis audio recordings is the first listed.

NCT06050083 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06050083 about?

NCT06050083 is a clinical study titled "Digital Clinical Hypnosis for Chronic Pain Management". This ClinicalTrials.gov posting contains two randomized controlled trials. The study procedures were identical, except Study 1 was funded by NIH and enrolled adults with chronic low back pain, whereas Study 2 was funded by the UW Department of Rehabilitation Medicine and enrolled adults with any typ...

What is the current status of trial NCT06050083?

This trial is currently completed. It is a NA study. The enrollment target is 100 participants. The study started on 2024-01-04. Estimated completion is 2024-09-15.

What interventions are being tested in trial NCT06050083?

The interventions under investigation include: Hypnosis audio recordings (BEHAVIORAL).

Who is sponsoring clinical trial NCT06050083?

This trial is sponsored by University of Washington, which has 1,048 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06050083's enrollment target sits among peer trials

100 840th of 2000 higher than 1,081 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01048281 · 100 participants

    Clinical & Pathological Studies of Upper Gastrointestinal Carcinoma

  • NCT01161199 · 100 participants

    The Use of Leukapheresis to Support HIV Pathogenesis Studies

  • NCT01327690 · 100 participants · Early Phase 1

    Mental Health in Veterans and Families After Group Therapies

  • NCT01730781 · 100 participants

    Imaging Cannabinoid Receptors Using Positron Emission Tomography (PET) Scanning

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06050083, the US trial registry maintained by the National Library of Medicine. NCT06050083 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.