Evaluation of the Future of Adolescents and Young Adults Received in an Early Care System (ReFSEF)

Fondation Santé des Étudiants de France

Status: Unknown

Conditions: Psychological Distress

Treatments: Other: monitoring naturalistic of cohort

Study type: Observational

Funder types: Other

Identifiers

NCT05163678

FSEF

Details and patient eligibility

About

This is a prospective clinical epidemiology study based on the naturalistic follow-up of a cohort of 1 500 young people aged 11 to 25 presenting consecutively over the course of one year at the Relais d'Ile de France.

Young people will be assessed on entry into the system (T0), at the end of the follow-up (T1) and 6 months after the end of the follow-up (T6).

Full description

Psychic suffering is very common among young people; a public health issue in France is to improve its early identification and treatment. To this end, the Fondation Santé des Etudiants de France (FSEF) has developed ambulatory systems in France called "Relais Collégiens-Lycéens-Etudiants" offering adolescents and young adults a reception, evaluation and support or a quick referral.

The FSEF Relay system allows a wide range of subjects to benefit from rapid support for a situation of mental suffering, which specialized care structures cannot do. In fact, first of all, if the school teams and the entourage are not made aware of the need to be attentive to psychological suffering, it is not detected, then when it is, most of these young people are not. not addressed out of reluctance from those around them or from the young person himself who refuse to go to psychiatric care experienced as stigmatizing; then, when young people are referred to care structures, consultation times are unsuitable (saturated structures) while these young people need a rapid response. The impact of early detection systems in adolescence has been little studied, this research proposes to initiate such an approach on a large panel of young people from a systematic evaluation, by evaluating the future in the short and medium term.

This research proposes to assess the impact of these devices. T his is a prospective clinical epidemiology study based on the naturalistic follow-up of a cohort of 1,500 young people aged 11 to 25 presenting consecutively over the course of one year at the 5 Relais d'Ile de France. Young people will be assessed on entry into the system (T0), at the end of the follow-up (T1) and 6 months after the end of the follow-up (T6). The data collected will be:

• The state of health (including mental health, somatic health and drug consumption), lifestyle and education and social adaptation through clinical assessment and self-questionnaires completed by young people:
• The clinical assessment includes the following elements: the severity of the psychological suffering (CGI, Global Clinical Impression), the psychosocial impact (SOFAS, Social and Occupational Functioning Assessment Scale) and the diagnosis of mental disorder according to the ICD 10 (International Classification) 10th Revision) when relevant.
• The self-questionnaires assess psychological suffering (K10, Kessler scale 10 items), social functioning (WSAS, Work Social Adjustment Scale) as well as satisfaction with the care provided (CSQ-8, Client Satisfaction Questionnaire 8 items, and Likert scale, at T1 and T6).
• The EDGAR grid (Interview, Approach, Group, Support, Meeting) to quantify the care offered at the Relais and their cost.
• The orientation that may be offered following this support

Enrollment: 1,500 estimated patients

Sex: All

Ages: 11 to 25 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• All adolescents, young adults in the age group 11-25 years,
• Presenting ill-being or psychological suffering, living in the health area concerned,
• Arriving alone or accompagniead at the "Realis" during the sudy period
• Agreeing to participate.

Exclusion criteria

• Young people outside the 11-25 age group,
• Parents and children who do not speak French or who cannot read or write.
• Young people in crisis situations requiring immediate hospitalization without consultation at the Relais.
• Refusal to participate

Trial design

1,500 participants in 1 patient group

patient group

Description:

All adolescents or young adults presenting for a consultation in the FSEF "Relais" systems. They will be assessed upon entry into the device (T0), at the end of the follow-up (T1) and 6 months after the end of the follow-up (T6).

Treatment:

Other: monitoring naturalistic of cohort