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Completed

NCT Number: NCT04559633

Cognitive and Behavioral Therapy in School Refusal

Anxious school refusal (ASR) is a common disorder which concerns more and more adolescents who are at worse completely absent from school. A specific ambulatory cognitive and behavioral therapy (CBT) program has been established to gradually reintegrate the child back into the school environment with a multidisciplinary team. Alongside school reintegration assessment, the child's overall ability to function and anxiety levels will be measured before and after the program with additional assessments made after a further 6 and 12 months have elapsed.

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Key information

Age range

10 year–16 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Montpellier University Hospital

Montpellier, 34295, France

About this study

ASR concerns children and adolescents who feel anxiety about going to school. Some are totally absent, some just have difficulty remaining in school for the entire day, or go to school following behavioral problems such as morning tantrums or psychosomatic complaints. Anxiety disorders are the main diagnostic underlying this behavioral problem, with one or many anxiety disorders associated (i.e. separation anxiety disorder, panic disorder, social anxiety disorder, generalized anxiety disorder or specific phobia). ASR causes much distress to the child, the parents, and the school personnel and interferes with social and educational development. Children with severe or chronic school refusal appear to have a long-term risk of adult mental health issues (e.g. anxiety, depression). Studies about ASR are few, and nonexistent in France. ASR occurs in approximately 1% of all school-aged children, and 5% of all clinic-referred children, is equally common in both boys and girls but more frequent in adolescents. Recommendations for anxiety disorder treatment in youth is psychotherapy. CBT, especially exposure-based, is the intervention that is supported by numerous, randomized, controlled trials in this area. But concerning ASR, there are few studies.

A specific ambulatory therapeutic CBT program for totally absent from school adolescents is established within the children and adolescent psychiatric unit in the University Hospital of Montpellier, France. The unit has implemented CBT techniques to gradually reintegrate the child back into the school environment. This program will be implemented in 3 other child and adolescent psychiatry centers (Marseille, Béziers and Nîmes).

The main objective of this study is to evaluate the efficiency of a CBT program on the return back to school.

Secondary objectives are:

  • To evaluate the feasibility in implantation of this program
  • To describe the characteristics of adolescents
  • To assess the initial severity of mental disorders and the evolution of these disorders
  • To describe the evolution of patient anxiety
  • To describe the evolution of the overall functioning
  • To evaluate the efficiency on the return back to school at 6 and 12 month after intervention.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adolescents between 10 and 16 years old registered in French college (6è to 3è),
  • Anxious school refusal based on Berg's criteria,
  • Completely dropped out from school (>5 consecutive days of school nonattendance, absenteeism < 12 months),
  • Anxiety disorder as a principal diagnosis (DSM 5)(MINI -S KID),
  • Adolescents want to return to school,
  • Signed consent by parents and adolescents

Exclusion criteria

  • Intellectual disabilities
  • Autism spectrum disorder
  • Learning disabilities that causes emotional trouble and being the primary cause of teenagers dropping out of school.
  • Conduct disorder (DSM 5)
  • Ongoing psychotherapeutic care that the parents or the adolescent would not wish to suspend
  • Participation in other ongoing research
  • Pregnancy
  • Patient not benefiting from a social security scheme

Treatment and study plan

cognitive and behavioral therapy (CBT)

Other

The CBT program is delivered by a multidisciplinary team with 4 half day hospitalization that includes individual, group CBT and education time (2 hours per day delivered by the teacher). Participants have homework to do in their own time at home.

CBT is a manualized program with anxiety psychoeducation, stress management, cognitive restructuration, problem solving techniques, progressive exposure, assertiveness exercises and self-esteem work.

Primary outcomes

  1. School continue reintegration

    Time frame: 46 months

    The return back to school next year : school continue reintegration (number of hours the adolescent attended school > 80% of the number of hours expected for each patient

Secondary outcomes

  1. Types of anxiety disorders according to the DSM 5

    Time frame: 46 months

    The questionnaire Mini-International Neuropsychiatric Interview for Children and Adolescents (MINI-S KID) is completed with parents and the adolescent

  2. Presence of comorbidities

    Time frame: 46 months

    Presence of comorbidities is evaluated by the questionnaire Mini-International Neuropsychiatric Interview for Children and Adolescents (MINI-S KID) completed with parents and the adolescent

  3. Initial severity of mental disorders and the evolution of these disorders

    Time frame: 46 months

    Mesure thanks to the Clinical Global Impression (CGI) scale.

  4. Anxiety assessment

    Time frame: 46 months

    Mesure thanks to the Anxiety and Phobia Behavioural (ECAP) Scale

  5. Anxiety assessment

    Time frame: 46 months

    Mesure thanks to the scales Revisited Children's Manifest Anxiety scale (RCMAS)

  6. Anxiety assessment

    Time frame: 46 months

    Mesure thanks to the scales Multidimensional Anxiety Scale for Children (MASC)

  7. Global functioning

    Time frame: 46 months

    Mesure thanks to the scale Children's global Assessment (C GAS) Scale

  8. School attendance time month by month

    Time frame: 46 months

Sponsors and collaborators

Lead sponsor

University Hospital, Montpellier

Other

Registry information

Official study title

Anxious School Refusal in Adolescents: Efficiency of a Cognitive and Behavioral Therapy (CBT) Day Hospital Program

Acronym: RSA-Coll

Important dates

Study start
2020
Primary completion
2023
Study completion
2024
First posted
Sep 23, 2020
Registry last updated
Jul 18, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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