NCT07369245

Brief Summary

Many patients are considering the use of so-called "hypnosis" treatments in the field of addictions. However, these techniques lack sufficient levels of evidence with regard to the standards required by Evidence-Based Medicine. In other domains, however, hypnosis has demonstrated an interesting level of evidence, particularly in pain management. The investigators will focus on the "Techniques for Activating Consciousness" (TAC), which represent an optimized therapeutic approach derived from hypnotic therapy.

Trial Health

63
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
98

participants targeted

Target at P50-P75 for not_applicable

Timeline
20mo left

Started Apr 2026

Geographic Reach
1 country

2 active sites

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress4%
Apr 2026Jan 2028

First Submitted

Initial submission to the registry

December 30, 2025

Completed
28 days until next milestone

First Posted

Study publicly available on registry

January 27, 2026

Completed
3 months until next milestone

Study Start

First participant enrolled

April 15, 2026

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 15, 2027

Expected
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 15, 2028

Last Updated

April 16, 2026

Status Verified

November 1, 2025

Enrollment Period

1.2 years

First QC Date

December 30, 2025

Last Update Submit

April 15, 2026

Conditions

Keywords

Hypnotic therapyTechniques for Activating Consciousness (TAC)Alcohol addiction

Outcome Measures

Primary Outcomes (1)

  • The patient's ability to control alcohol consumption during outpatient follow-up in a CSAPA

    The main outcome measure will be the number of weeks to achieve the targeted goal between T0 (first consultation when the objective is set) and M6 (cumulative time).

    6 months

Secondary Outcomes (2)

  • Controlling addictive behavior in both groups

    12 months

  • Evaluation criteria for the TAC group

    12 months

Study Arms (2)

Control

NO INTERVENTION

TAC intervention

EXPERIMENTAL
Behavioral: TAC intervention

Interventions

Patients receiving TAC (Techniques for Activating Consciousness) intervention in addition to standard care

TAC intervention

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Adult patients consulting for an alcohol-related addiction problem at the CSAPA of Versailles (sites in Versailles, Trappes, Rambouillet) or at the Centre Hospitalier des 4 Villes (day hospital or CSAPA in Sèvres)
  • Patients must meet at least 4 of the 11 DSM-5 criteria (Annex 2), corresponding to moderate to severe addiction
  • Patients must be affiliated with the French social security system

You may not qualify if:

  • Refusal to participate
  • Decompensated psychiatric pathology contraindicating therapy:
  • Severe cognitive impairment, evidenced by inability to perform the clock-drawing test (draw the clock face, place the numbers, and set the hands to 11:10)
  • Adults legally protected under French law (deprivation of liberty, legal safeguard, guardianship, curatorship)
  • Inability to understand French

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Hospital Versailles

Le Chesnay, 78150, France

Location

CH des 4 Villes

Sèvres, 92310, France

Location

MeSH Terms

Conditions

Alcoholism

Condition Hierarchy (Ancestors)

Alcohol-Related DisordersSubstance-Related DisordersChemically-Induced DisordersMental Disorders

Central Study Contacts

Claire FARINA, Dr

CONTACT

Nadia YOUNES, Dr

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Investigator Coordonnator

Study Record Dates

First Submitted

December 30, 2025

First Posted

January 27, 2026

Study Start

April 15, 2026

Primary Completion (Estimated)

July 15, 2027

Study Completion (Estimated)

January 15, 2028

Last Updated

April 16, 2026

Record last verified: 2025-11

Locations