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🏛️ Verified NIH Protocol • Sourced via U.S. National Library of Medicine (Last Synced: 2025-01-28)

Self-hypnosis Training for Chronic Pain Management

🟢 Recruiting Protocol / Phase N/A 📋 Clinical Research Protocol Sponsor: Ciusss de L'Est de l'Île de Montréal

🩺 Protocol Summary

Title: Self-hypnosis training in chronic pain management: A pilot study Our primary objective concerns the effect of hypnosis intervention on change in 24h pain between T0 (pre-intervention) and T4 (3-month follow-up). The secondary objectives concern the effects of the intervention on (i) change in 24h pain between T0 and T5 (6-month follow-up), (ii) changes from T0 in measures of the functional impact of pain, (iii) changes from T0 in anxiety-depression scores and (iv) changes from T0 in quality of life. The study design is a Randomized efficacy pilot study. The study focuses on patients practicing self-hypnosis within HMR groups. The study population is pain clinic patients. The sample size is 60 pain clinic patients. Study duration: February 2024 - December 2024. Center responsible for the study: Centre de Recherche de l'Hôpital Maisonneuve-Rosemont (CR-HMR) - CEMTL, Montreal, Quebec, Canada. Adverse events: none expected.

Primary Research Facility: 5415 Bd de l'Assomption (Montreal, Quebec)

📋 Basic Study Criteria & Logistics Checklist

0 of 3 Checked

Review these 3 basic logistical and protocol criteria extracted from the public NIH record. (This is a preliminary logistical checklist, not an official clinical eligibility determination).

📍 Primary Site Map

Site: 5415 Bd de l'Assomption — Montreal, Quebec

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🏛️ Official Government Provenance

NIH ClinicalTrials.gov Protocol Record

NCT Identifier: NCT06279650 • Last Synced: 2025-01-28
View on ClinicalTrials.gov ↗
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