Telephone Support vs. Self-guidance in an Internet-based Self-administered Psychological Program to Address Depression

NCT06230237 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2024-01-30

No results posted yet for this study

Summary

Depression is a first level problem that poses a challenge for Primary Care (PC). The overload of care in this area requires lower-cost and more accessible alternatives. Internet-based self-applied cognitive behavioral treatments (CBCT) have demonstrated their efficacy and added advantages. The "Smiling is fun" program has been validated in Spanish PC and has demonstrated its usefulness and cost-effectiveness. Previous studies have shown that professional support or guidance increases the results of the TCCI.

The aim of the present study is to contrast, by means of a randomized controlled trial, aims to examine the effectiveness, adherence rates, and implementation process of Smiling is Fun to address depression in a PC setting considering the influence of telephone support vs no support.

Ultimately, the results of the study could help in the uptake of sustainable resources so that the population could gain better access to psychological interventions in mental health services.

Conditions

Interventions

BEHAVIORAL

Smiling is fun + professional support

Participants will receive an intervention called Smiling is Fun; a cognitve-conductual online program with the most effective psychological procedures for depression and other techniques to promote coping ability, emotional regulation and resilience along 8 modules. While they do the online program, they will receive periodically professional support. The professional support will be contacts of 20 minutes long, will take place every two weeks and will last 3 months.

BEHAVIORAL

Smiling is fun

Participants will receive an intervention called Smiling is Fun; a cognitve-conductual online program with the most effective psychological procedures for depression and other techniques to promote coping ability, emotional regulation and resilience along 8 modules.

Sponsors & Collaborators

  • Hospital Francesc de Borja

    collaborator UNKNOWN
  • Universitat Jaume I

    lead OTHER

Principal Investigators

  • Azucena García Palacios · Universidad Jaume I

  • Pedro Vera Albero · F.E.D. Psicología Clínica Unitat de Salut Mental Hospital Francesc de Borja

  • Raquel Escriva Sanchis · F.E.D. Psicología Clínica Unitat de Salut Mental Hospital Francesc de Borja

  • Clara Bretó García · F.E.D. Psicología Clínica Unitat de Salut Mental Hospital Francesc de Borja

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-06-01
Primary Completion
2024-06-01
Completion
2024-12-30

Countries

  • Spain

Study Locations

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Entities

Diseases

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 NCT06230237 on ClinicalTrials.gov