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Clinical Trials/NCT04179526
NCT04179526
Completed
Not Applicable

The Efficacy and Mechanisms of Change of a Transdiagnostic Internet-delivered REBT Intervention for Adolescents With Internalizing Problems: A Randomized Controlled Trial

Babes-Bolyai University1 site in 1 country106 target enrollmentJanuary 25, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anxiety Disorders
Sponsor
Babes-Bolyai University
Enrollment
106
Locations
1
Primary Endpoint
Internalizing problems measured with the Youth Self-Report 11/18 (YSR; Achenbach & Rescorla, 2001)
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

To investigate the efficacy and mechanisms of change of an Internet-delivered transdiagnostic REBT intervention for adolescents with internalizing problems.

Detailed Description

The main objectives of this study are to evaluate the efficacy and mechanisms of change of an Internet-delivered Rational Emotive Behavior Therapy for adolescents (12-15 years) diagnosed with a principal anxiety or depressive disorder according to DSM-5 criteria. Participants will be randomly allocated to one of the two groups: experimental (REBTonAd) and waitlist control. The intervention is structured in 8 modules and will be delivered over six weeks. Assessments will be conducted at four time points: baseline, post-treatment, 3-month follow-up, and 6-month follow-up.

Registry
clinicaltrials.gov
Start Date
January 25, 2020
End Date
December 30, 2022
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Babes-Bolyai University
Responsible Party
Principal Investigator
Principal Investigator

Anca Dobrean

Professor

Babes-Bolyai University

Eligibility Criteria

Inclusion Criteria

  • Age between 12 and 15 years
  • A principal diagnosis of Social Anxiety Disorder, Generalized Anxiety Disorder, Panic Disorder, Persistent Depressive Disorder, or Major Depressive Disorder as defined by DSM-5 (APA, 2013)
  • Not currently following another treatment (psychotherapy, pharmacological treatment);
  • Internet access
  • Ability to read and write Romanian

Exclusion Criteria

  • Suicidal ideation
  • Severe depression
  • Any physical and mental health acute problem that requires hospitalization
  • Diagnosed with autism spectrum disorder, psychosis, bipolar disorder or mental disability

Outcomes

Primary Outcomes

Internalizing problems measured with the Youth Self-Report 11/18 (YSR; Achenbach & Rescorla, 2001)

Time Frame: Baseline, Immediately after the intervention (an expected average of 6 weeks), 6-month follow-up

Change in self-reported internalizing problems from baseline to post-treatment, at 6 months post treatment. Higher scores indicate higher levels of internalizing problems.

Secondary Outcomes

  • Automatic Thoughts QuestionnaireShort Version (ATQ-SV; Netemeyer et al., 2002)(Baseline, Immediately after the intervention (an expected average of 6 weeks), 6-month follow-up)
  • The child and adolescent scale of irrationality (CASI; Bernard & Cronan, 1999)(Baseline, Immediately after the intervention (an expected average of 6 weeks), 6-month follow-up)
  • The Questionnaire for Measuring Health-Related Quality of Life in Children and Adolescents, The Revised Version - adolescent version (Kiddo-KINDL; Ravens-Sieberer, & Bullinger, 1998)(Baseline, Immediately after the intervention (an expected average of 6 weeks), 6-month follow-up)
  • The Adolescent Peer Relations Instrument (APRI; Parada, 2000)(Baseline, Immediately after the intervention (an expected average of 6 weeks), 6-month follow-up)
  • Principal diagnosis based on Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5) criteria(Baseline, 6-month follow-up)

Study Sites (1)

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