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Not yet recruiting NCT07020013

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

Observational School Phobia

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: School Phobia. Basic parameters: 12 years — 18 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 →

Overview

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.

Primary outcome measures

  • Anxious school refusal [Time frame: Month 10]
Secondary outcome measures (6)
  • Obsessive-compulsive disorder assessment [Time frame: Month 10]
  • Anxiety disorder assessment [Time frame: Month 10]
  • depressive disorder assessment [Time frame: Month 10]
  • Post traumatic Stress disorder assessment [Time frame: Month 10]
  • Attention Deficit Hyperactivity disorder assessment [Time frame: Month 10]
  • Schooling method [Time frame: Month 10]

Eligibility criteria

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

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

Study design

Observational model
Cohort

Study locations

France · 1 center
  • Clinique des 3 cyprès — La Penne-sur-Huveaune

Identifiers

NCT: NCT07020013 · 2025-A00523-46

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗