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Study identifier: NCT05569018 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Efficacy of a Transdiagnostic Group Treatment for Emotional Disorders Applied in Blended Format: a Controlled Study.

Condition: Anxiety Disorders · Depressive Disorders  ·  Sponsor: Universitat Jaume I

PhaseNA
Planned participants144
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study will consist in a randomized controlled clinical trial (RCT) to test the efficacy of a blended group transversal protocol (BLGr-TP) compared to a face-to-face group transversal protocol (FFGr-TP). The main aims of the study are the following: * To analyze the differential efficacy of the BLGr-TP versus the FFGr-TP for the treatment of emotional disorders in aspects of clinical measures, as well as in terms of retention and dropout rate and adherence. * To analyze the differential acceptability of the BLGr-TP versus the FFGr-TP for the treatment of emotional disorders. In addition, it is intended to carry out a study of mediators and moderators of the efficacy of both interventions. The established hypotheses in relation to the main goals are: * Both treatment modalities (FFGr-TP and BLGr-TP) will achieve improvements in the symptoms of emotional disorders, reflected in the scores of the clinical measures. * The BLGr-TP will show equivalent efficacy to the FFGr-TP. * The BLGr-TP will show an acceptability comparable to the face-to-face protocol. Both modalities will be well valued by the participants. * In both treatment modalities, the changes achieved are expected to be maintained over time (3, 6 and 12 months).

This description comes directly from the study's public registry record.

Talk to the study team

Juana María Bretón-López, Dr.  ·  +34 964387642  ·  breton@uji.es

Azucena García-Palacios, Dr.  ·  +34 964387640  ·  azucena@uji.es

Always discuss trial participation with your own doctor first.

Locations (1)

Jaume I University, Castellón, SpainCastellon, Castellón, SpainRecruiting

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Source record: clinicaltrials.gov/study/NCT05569018