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Clinical Trials/NCT07020013
NCT07020013Not yet recruitingNot Applicable

Evaluation of the Effectiveness of Day Hospital Care for Adolescents With Anxious School Refusal

GCS Ramsay Santé pour l'Enseignement et la Recherche1 site in 1 country80 target enrollmentStarted: September 1, 2025Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
80
Locations
1
Primary Endpoint
Anxious school refusal

Study Overview

Brief Summary

The objective of the study is to evaluate the benefit of day care in a child psychiatric hospital on the return to school and on the development of child psychiatric disorders associated with Anxious Social Refusal.

Detailed Description

This is a prospective, longitudinal, single-center observational cohort study carried out on a population of patients followed in a day hospital for anxious school refusal.

Participating physicians will have the opportunity to recruit their patients over a 12-month period. All enrolled patients will be followed for a minimum of 10 months. The study will be completed as soon as the last enrolled patient has completed a final assessment.

Aside from the baseline visit, each patient will be assessed only once at 10 months. During each patient visit with the investigating physician, the physician will complete an assessment on the electronic CRF.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
12 Years to 18 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients aged 12 to 18 years
  • •Patients with anxious school refusal, defined by a score ≥ 41 on the SCREEN scale
  • •Patients receiving day hospital care
  • •Patients who have been informed and whose parents (or holder(s) of parental authority) have agreed to their participation in the study and have not objected to the use of their health data

Exclusion Criteria

  • •Patients with a mental disability or any other reason that may hinder the understanding or strict application of the protocol
  • •Patients not affiliated with the French social security system
  • •Patients under guardianship

Outcomes

Primary Outcomes

Anxious school refusal

Time Frame: Month 10

The primary endpoint is based on the change in the SCREEN scale score between inclusion and the end of the study. A 20% improvement in this score will be considered as evidence of a benefit from day hospital care on anxious school refusal.

Secondary Outcomes

  • Obsessive-compulsive disorder assessment(Month 10)
  • Anxiety disorder assessment(Month 10)
  • depressive disorder assessment(Month 10)
  • Post traumatic Stress disorder assessment(Month 10)
  • Attention Deficit Hyperactivity disorder assessment(Month 10)
  • Schooling method(Month 10)

Investigators

Sponsor
GCS Ramsay Santé pour l'Enseignement et la Recherche
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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