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A Blended Intervention for Adjustment Disorder.

NCT05464121 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 41

Last updated 2026-02-10

No results posted yet for this study

Summary

The aim of this study is to evaluate the feasibility (including usability and satisfaction) and preliminary effectiveness of a blended intervention for Adjustment Disorder. This intervention combines a self-applied Internet-based program (TAO) with face-to-face sessions with a therapist via videoconference.

Conditions

  • Adjustment Disorders

Interventions

BEHAVIORAL

• Blended treatment for AjD combining a self-applied Internet-based program (TAO) with face-to-face sessions via videoconference.

The self-applied Internet-based program called TAO is accessible online from the platform https://psicologiaytecnologia.labpsitec.es. It is organised into 7 sequential modules of approximately 60 minutes. The patient will do a treatment module every 10-12 days, plus an individual session via videoconference with a therapist (approximately 20-30 minutes long). During these sessions, the therapist will explain the main contents of each module, resolve doubts and motivate the patient to continue with the therapy. It takes about 12 weeks to complete the intervention. TAO is the optimised version of the original intervention protocol for AjD developed by Botella et al. by Botella et al. (2008) and includes the following therapeutic components: psychoeducation, emotion regulation techniques, exposure, problem-solving techniques, Mindfulness, acceptance and elaboration of the stressful event, positive psychology strategies and relapse prevention.

Sponsors & Collaborators

  • Universitat Jaume I

    lead OTHER

Principal Investigators

  • Soledad Quero, Ph.D · Department of Basic, Clinical Psychology and Psychobiology, Universitat Jaume I, Castellón, Spain

  • Pim Cuijpers, Ph.D · Amsterdam Public Health Research Institute, Amsterdam, The Netherlands

  • Sara Fernández Buendía, Ph.D student · Department of Basic, Clinical Psychology and Psychobiology, Universitat Jaume I, Castellón, Spain

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-11-18
Primary Completion
2025-06-01
Completion
2025-11-01

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05464121 on ClinicalTrials.gov