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RecruitingNCT05609474TRYADUpdated Jul 30, 2025

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

An observational study in Addiction, sponsored by Hôpital le Vinatier. Recruiting at 1 site in France. Open to participants aged 12 Years to 25 Years. Per ClinicalTrials.gov, last updated 2025-07-30.

Sponsored by Hôpital le Vinatier · Observational

From the registry’s dates

  • Started Feb 2023; still recruiting 3 years 9 months later.

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Study type
Observational
Model
Ecologic or community
Time perspective
Other
Enrollment
1,430
Ages
12 Years to 25 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-15

Among 77 studies in Behavior, Addictive with a site in France — 33 open to participants now, 34 under way, none of them phase 3. Behavior, Addictive · France.

Planned enrollment
7th of 43
1,430 · median 170
Started
2023
with 6 others
Observational
43 of 77
20 open now
Primary completion
2027-02
later than 17 of 33 live
Registered
47th of 77
by date

Among the 77 studies in Behavior, Addictive with a site in France, this one is the 7th largest by planned enrollment of the 43 observational ones that give a count, is one of 7 that started in 2023, is one of 43 observational ones, reaches primary completion later than 17 of the 33 other live ones, and was the 47th registered.

Behavior, Addictive

521 studies on the registry are indexed under Behavior, Addictive; 124 are open to participants now.

Browse Behavior, Addictive studies →

Open to participants now

33 of the 77 studies in Behavior, Addictive with a site in France are open now. Recruiting first, the newest first:

27 more — sign in →

All 33 open studies →

A study can be open while its sites in France have not opened yet or have stopped. Only those recruiting at a site in France →

Who these studies take

Of the 80 Behavior, Addictive studies recruiting now, 44 (55%) set no upper age limit and 34 (43%) stop at 75 or younger; 7 take children under 18; 24 take healthy volunteers.

This study: 12 Years to 25 Years · all sexes · no healthy volunteers.

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02

Study summary

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.

Read the 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
03

Conditions studied

  • Addiction

Browse trials for

04

Who can participate

Ages eligible
12 Years to 25 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Young people with addiction problems

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

  • inability to reach by phone
  • Insufficient french level
05

Study design

Observational model
Ecologic or community
Time perspective
Other
Enrollment
1,430 participants (estimated)
Target follow-up
1 Year
Patient registry
Yes

Groups and cohorts

  • Users (adolescents or young adults)

    1430 users (adolescents and young adults) with addiction problems and consulting CJC for the first time

  • Caregivers

    715 caregivers

  • Consultations Jeunes Consommateurs CJCs

    Initial survey (month 0) of participating CJCs: assessment of the "structural" characteristics of the CJCs (type of CJC (hospital, association), urban/rural area, number of users, number of consultations per month, type of workers...) \- Telephone interview at the 6th and 12th month: assessment of variables related to the user's pathway (referral to a specialized medical or social service…)

06

What researchers measure

Primary outcomes

  1. Evolution in Global Appraisal of Individual Needs Short Screener (GAIN-SS) score from first assessment to 12-month assessment

    The GAIN-SS scale is a self-administered questionnaire whose responses will be collected by telephone in a standardized manner for all included participants

    Time frame: Two days ( at month 0 and month 12)

Secondary outcomes

  1. For users: Measurement of satisfaction with CJC use, assessed at 12 months, using the Client Satisfaction Questionnaire - 8 (CSQ-8)

    Evaluation of the secondary criterion: Client Satisfaction Questionnaire - 8 (CSQ-8)

    Time frame: One day (at month 12)

  2. For caregivers : Measurement of satisfaction with CJC use, assessed at 12 months, using the Client Satisfaction Questionnaire - 8 (CSQ-8)

    Client Satisfaction Questionnaire - 8 (CSQ-8)

    Time frame: One day (at month 12)

  3. For caregivers : Evolution in Strengths and Difficulties Questionnaire (SDQ) score from first assessment to 12-month assessment

    Strengths and Difficulties Questionnaire (SDQ)

    Time frame: Two days (at month 0 and month 12)

  4. For all subjects included : Qualitative study : to assess their experience of the CJC's contribution to their needs and expectations

    Qualitative study on a sub-sample of caregivers

    Time frame: One day (month 12)

07

Study locations

1 of 1 sites recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Feb 2023 (actual). Primary completion is estimated for Feb 2027, 48 months after the start.

Of 46 non-industry observational studies under Behavior, Addictive, half reached primary completion within 40 months of starting (the median), counting those still running; a quarter within 20 and three quarters within 111. This study's planned 48 months is above that.

Counting every sponsor, half of 49 studies reached it within 40 months; a quarter within 20 and three quarters within 73.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 1, 2022
First posted
Nov 8, 2022
StartActual
Feb 15, 2023
Primary completionEst.
Feb 15, 2027
CompletionEst.
Oct 1, 2028
Last update
Jul 30, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 30, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05609474
Responsible party
Sponsor
First posted
Nov 8, 2022
Start date
Feb 15, 2023
Primary completion
Feb 15, 2027 (estimated)
Completion
Oct 1, 2028 (estimated)
Last update
Jul 30, 2025

Study contacts

LOUIS FERDINAND LESPINE
Contact
louis-ferdinand.lespine@ch-le-vinatier.fr
0033437913461
VERONIQUE VIAL
Contact
veronique.vial@ch-le-vinatier.fr
0033437915522
Benjamin ROLLAND, PhD
principal investigator · Centre Hospitalier le Vinatier

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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