Cognitive Therapy for Unipolar Depression: Efficacy of a Dilemma-Focused Intervention

NCT01542957 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 128

Last updated 2017-03-22

Study results available
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Summary

The purpose of this study is to determine the efficacy of a brief psychological intervention focused on the personal dilemmas identified for each depressive patient. For that, this intervention is combined to group cognitive therapy (an already proven efficacious format) and compared to cognitive individual therapy.

Conditions

Interventions

BEHAVIORAL

Combined Cognitive Behavioral and Dilemma-Focused Therapy

7 2-hour sessions of Group Cognitive Behavioral Therapy for Depression + 8 individual sessions of a Dilemma-Focused Intervention + 1 3-hour final group session. Manualized.

BEHAVIORAL

Cognitive Behavioral Therapy for Depression

Cognitive Behavioral Therapy for Depression. Format: 7 2-hour sessions in group + 8 individual sessions + 1 3-hour final group session. Manualized.

Sponsors & Collaborators

  • National Distance Education University (UNED)

    collaborator UNKNOWN
  • University of Minho

    collaborator OTHER
  • University of Hertfordshire

    collaborator OTHER
  • University of Bern

    collaborator OTHER
  • University Ramon Llull

    collaborator OTHER
  • Institut Trastorn Límit

    collaborator UNKNOWN
  • Hospital de Mataró

    collaborator OTHER
  • Fundació Institut de Recerca de l

    collaborator UNKNOWN
  • Associació Centre de Salut Mental Nou Barris

    collaborator UNKNOWN
  • Fundacion IMIM

    collaborator OTHER
  • EAP Poble Sec

    collaborator UNKNOWN
  • Associació Catalana de Terapies Cognitives

    collaborator UNKNOWN
  • Sant Pere Claver Fundació Sanitaria

    collaborator UNKNOWN
  • University of Barcelona

    lead OTHER

Principal Investigators

  • Guillem Feixas, Ph.D. · University of Barcelona

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-11-30
Primary Completion
2014-11-30
Completion
2015-05-31

Countries

  • Spain

Study Locations

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Entities

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 NCT01542957 on ClinicalTrials.gov