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Recruiting NCT05609474

Trajectories and Reactions of Users and Relatives Consulting French Youth Addiction Services

Observational Addiction

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Addiction. Basic parameters: 12 years — 25 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Trajectories and Reactions of Users and Relatives Consulting French Youth Addiction Services (Consultations Jeunes Consommateurs)

Overview

In France, the "Consultations Jeunes Consommateurs" (CJC) are the services specialized in the reception of young people for addiction problems. There are more than 500 CJCs throughout France. Depending on the situation, the CJC develops an early intervention strategy aimed either at reducing the risk of developing an addiction or at accelerating entry into appropriate care. The CJCs also meet with family members or professionals who may also independently request help or advice. Set up by the State since 2004, the action of the CJCs has never been formally evaluated. Only descriptive studies, carried out by the French Observatory of Drugs and Drug Addiction (OFDT), have made it possible to better understand the profile of people who consult CJCs. However, no longitudinal study has yet been carried out to understand the factors associated with the overall evolution of users consulting CJCs, nor with the level of satisfaction of users and those around them. Such objectives are complex, due to the diversity of situations encountered in CJCs and the heterogeneity of the CJCs themselves.

Detailed description

This multicenter study will be open to 19 CJC (Consultations jeunes Consommateurs), based on a pre-selection by the partners of structures that are particularly willing to participate in the study (Fédération Addictions, Addictions-France).

However, other CJCs may be included depending on the progress of recruitment.

This recruitment of additional CJCs will be stratified to target a sample of CJCs representative of the CJCs on the metropolitan territory on the following characteristics:

* Region (13 major regions) * Rural or urban area, as defined by INSEE * Number of annual consultations

Primary outcome measures

  • Evolution in Global Appraisal of Individual Needs Short Screener (GAIN-SS) score from first assessment to 12-month assessment [Time frame: Two days ( at month 0 and month 12)]
Secondary outcome measures (4)
  • For users: Measurement of satisfaction with CJC use, assessed at 12 months, using the Client Satisfaction Questionnaire - 8 (CSQ-8) [Time frame: One day (at month 12)]
  • For caregivers : Measurement of satisfaction with CJC use, assessed at 12 months, using the Client Satisfaction Questionnaire - 8 (CSQ-8) [Time frame: One day (at month 12)]
  • For caregivers : Evolution in Strengths and Difficulties Questionnaire (SDQ) score from first assessment to 12-month assessment [Time frame: Two days (at month 0 and month 12)]
  • For all subjects included : Qualitative study : to assess their experience of the CJC's contribution to their needs and expectations [Time frame: One day (month 12)]

Eligibility criteria

Inclusion criteria

For users :

  • First consultation in CJC
  • From 12 to 25 years old

For caregivers :

  • First consultation in CJC (with or without the youth) or second consultation if accompanying a user
  • ≥ 18 ans

Exclusion criteria

  • inability to reach by phone
  • Insufficient french level

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Ecologic or community

Study locations

France · 1 center
  • Centre Hospitalier Le Vinatier — Bron

Identifiers

NCT: NCT05609474 · 2020-A01365-36

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗