An Internet-based Program for Prevention and Early Intervention of Adolescent Depression

May 29, 2018 updated by: Henry Daniel Espinosa Duque, CES University

A Randomized Controlled Trial of an Internet-based Program for Prevention and Early Intervention of Adolescent Depression

Major depression is a highly prevalent and severe mental disease. Interventions based on information and communication technologies (ICTs) generate innovative opportunities to prevent and to intervene early the depression in adolescents. In Colombia, there are few preventive mental health interventions scientifically oriented and seeking to demonstrate efficacy in context.

The purpose of this study is to determine whether an internet-based program is effective to prevent and to intervene early the depression in adolescents between 13 and 19 years of age in 8 schools of the Antioquia Region, Colombia .

Study design: A cluster-randomized clinical trial will be carried out with 600 adolescents. The efficacy, adherence, and acceptability of the internet-based program will be evaluated. A single-blind randomized controlled trial will be conducted with two arms, the intervention arm (n=300), which will receive an internet-based program for depression, and the TAU (Treatment As Usual) arm (n=300).

Study Overview

Status

Unknown

Conditions

Detailed Description

Major depression is a highly prevalent and severe mental disease that negatively alters the lives of people, their families, and their social environment.

Organizations that promote mental health policies have recognized the potential of new information technologies for the prevention and treatment of mental disorders. In this direction, information and communication technologies (ICTs) generate opportunities for increasing patient well-being through the use of on-line software. Such programs often include interactivity, self-monitoring, information materials (sometimes in multimedia format), and exercises on problem solving, recognition and challenging of dysfunctional thoughts, scheduling of activities, behavioral experiments, and other psycho-educational activities.

In Colombia, there are few preventive mental health interventions scientifically oriented and seeking to demonstrate efficacy in context.

The purpose of this study is to determine whether an internet-based program is effective to prevent and to intervene early the depression in adolescents between 13 and 19 years of age in 8 schools in the Antioquia Region, Colombia.

Study design: A cluster-randomized clinical trial will be carried out with 600 adolescents. The efficacy, adherence, and acceptability of the internet-based program will be evaluated. A single-blind randomized controlled trial will be conducted with two arms, the intervention arm (n=300), which will receive an internet-based program for depression, and the TAU arm (n=300).

Follow-up times: T = 0 baseline, T= 3 months (post-intervention), T=12 months.

Study Type

Interventional

Enrollment (Anticipated)

600

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Antioquia
      • Medellin, Antioquia, Colombia, 00000
        • Recruiting
        • Institucion Educativa Villaflora
        • Contact:
          • Fredy Tabares, Psychologist
          • Phone Number: (57) 4 2348424
      • Medellín, Antioquia, Colombia, 0000
        • Recruiting
        • Institucion Educativa El Pedregal
        • Contact:
          • Astrid Restrepo, Psychologist
          • Phone Number: 00 (57) 4 4274457
      • Medellín, Antioquia, Colombia, 050034
        • Recruiting
        • Institución Educativa El Corazón
        • Contact:
          • Lina M Vallejo, Psychologist

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

13 years to 18 years (ADULT, CHILD)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Young students in schools of Antioquia between 6 and 11 high school degree, with internet access and available psychological service, foreseeing that moderate or severe depressive symptoms may be found.

Exclusion Criteria:

  • Young students with high suicide risk defined by: score equal to or greater than 2 in question 9 of PHQ-9; students who are receiving at the time treatment with antidepressant drugs and / or currently attending psychotherapy.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: PREVENTION
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Internet-based program

Adolescents in the intervention will receive a tailored online program during 3 months.

Adolescents interact with the program via a monitoring e-mail that they receive every two weeks (Monitoring) and a website which allows them to access a number of links.

CUIDA TU ÁNIMO is an online program to adolescents that provides information, education and support related to the care of the mood.

Adolescents interact with the program via a monitoring e-mail that they receive every two weeks (Monitoring) and a website which allows them to access a number of links. The website have the following modules:

  1. What is 'CUIDA TU ÁNIMO': Description and definition of the program
  2. Psycho-educational information: Information about depression, its treatment, and opportunities for prevention
  3. How is your mood? (Monitoring): a) Online assessment of symptoms every two weeks during three months with the PHQ-3. b) Feedback
  4. Forums.
  5. Blog.
  6. Appointment (Chat or Phone call).
  7. Contact.
NO_INTERVENTION: Treatment as usual
-Waiting list control group.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from Baseline Depressive Symptomatology at 3 months and 12 months
Time Frame: Baseline, 3 months, 12 months
Depressive symptomatology measured with the Patient Health Questionnaire PHQ -9 [6]
Baseline, 3 months, 12 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from Baseline in Health Related Quality of Life at 3 and 12 months
Time Frame: Baseline, 3 months, 12 months
Health Related Quality of Life Questionnaire for Children and Young People KIDSCREEN-27 [7]
Baseline, 3 months, 12 months
Change from Baseline in anxious symptoms at 3 and 12 months
Time Frame: Baseline, 3 months, 12 months
Generalised Anxiety Disorder Assessment (GAD-7) [8]
Baseline, 3 months, 12 months
Change from Baseline in of depression at 3 and 12 months
Time Frame: Baseline, 3 months, 12 months
Self-Stigma of Depression Scale (SSDS) [9]
Baseline, 3 months, 12 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

May 11, 2018

Primary Completion (ANTICIPATED)

September 1, 2018

Study Completion (ANTICIPATED)

September 1, 2019

Study Registration Dates

First Submitted

May 18, 2016

First Submitted That Met QC Criteria

May 19, 2016

First Posted (ESTIMATE)

May 23, 2016

Study Record Updates

Last Update Posted (ACTUAL)

May 31, 2018

Last Update Submitted That Met QC Criteria

May 29, 2018

Last Verified

May 1, 2018

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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