Attachment and Prognostic Factor: the Implicit Approach

NCT04954027 | Not Yet Recruiting

• 1 other identifier: 2021-A00432-39
• Study Type: observational
• Target: 200
• Locations: 0 countries
• Sites: N/A

Brief Summary

This is a prospective longitudinal study aimed at better understanding the determinants of the prognosis of patients with substance dependence. 5 visits are planned during the study :

• the inclusion visit : during this visit the patient's non-opposition is obtained and then the patient answer to self-administered questionnaires online
• 4 telephone interviews for follow-up by investigator.

Conditions

Dependence Addictive

Keywords

implicit approach; post-weaning prognostic factor

Outcome Measures

Primary Outcomes (1)

• Implicit attachment and onsumption

  Assessment of the link between implicit attachment and changes in consumption after a 12-month follow-up

  12 months

Study Arms (1)

Patients with a use-related disorder weaning for a substance

Behavioral: Questionnaires

Interventions

Questionnaires BEHAVIORAL

5 visits are planned during the study : * the inclusion visit : during this visit the patient's non-opposition is obtained and then the patient answer to self-administered questionnaires online * 4 telephone interviews for follow-up by investigator

Patients with a use-related disorder weaning for a substance

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Probability Sample

Study Population

Patients with a use-related disorder weaning for a substance, supported within the addictology sector of Henri Laborit Hospital

You may qualify if:

• Patients between 18 and 65 years old
• Patients with a use-related disorder as defined by DSM5
• Patients weaning for a substance, supported within the addictology sector of Henri Laborit Hospital
• Having expressed non-opposition to participating in the study after receiving written information.

You may not qualify if:

• Person who cannot read or write
• Simultaneous participation in a therapeutic trial involving oxytocin
• Patients protected by law
• Patients who do not have French as their native language
• Patients who, in the opinion of the investigator, are unable to complete the questionnaires

Sponsors & Collaborators

• Centre Hospitalier Henri Laborit: lead

MeSH Terms

Conditions

Behavior, Addictive

Interventions

Surveys and Questionnaires

Condition Hierarchy (Ancestors)

Compulsive Behavior; Impulsive Behavior; Behavior

Intervention Hierarchy (Ancestors)

Data Collection; Epidemiologic Methods; Investigative Techniques; Health Care Evaluation Mechanisms; Quality of Health Care; Health Care Quality, Access, and Evaluation; Public Health; Environment and Public Health

Study Officials

• Wilfried SERRA, Dr

  Centre Hospitalier Henri Laborit

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Wilfried SERRA, Dr

CONTACT

0033 5 16 52 61 18; wilfried.serra@ch-poitiers.fr

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: June 29, 2021
• First Posted: July 8, 2021
• Study Start (Estimated): September 1, 2026
• Primary Completion (Estimated): September 1, 2028
• Study Completion (Estimated): September 1, 2028
• Last Updated: June 5, 2025

Record last verified: 2025-06

Data Sharing

• IPD Sharing: Will not share