Effects of an Educational Program on Depression Literacy and Stigma Among Secondary School Students in Jazan City

October 25, 2020 updated by: Hussain Darraj, University of Jazan

Effects of an Educational Program on Depression Literacy and Stigma Among Students of Secondary Schools in Jazan City

Depression is a serious mental health disease. It is generally characterized by sadness, loss of interest in activities, and decreased energy. Globally, it is estimated that almost 350 million people suffer from depression. In Saudi Arabia, literature suggested that prevalence of depression among boy's secondary school students in Abha city was 38.2%. Another study found that the prevalence of depression was 22.4 % as moderate, 7.3 % as severe and 3.7% as very severe, with a clear predominance prevalence of depression in girls as in boys (1.5 times). It is important to assess depression literacy including knowledge and beliefs about mental disorders among adolescent. A high level of mental health literacy on depression leads to a better understanding and outcomes of depressive disorders. Schools are a typical venue in which to embed mental health literacy because the school students are more familiar with educational activities. Studies concluded that educational intervention about depression literacy and destigmatization improves knowledge and may decrease stigma. Further research, intervention and activism are needed in the field of mental health in Arab countries to improve awareness of mental health problems.

Objectives: This study is aimed to measure the effect of educational intervention program about depression among secondary schools in Jazan city on depression literacy and stigma during the academic year 2015-2016.

The intervention: the intervention will held at each selected intervention school separately. The program will be over 2 weeks intervention as the following:

  • Educational strategies: 2 Lecture about depression 30 minutes supported by group discussion, brochures and display of posters with mental-health slogans on depression in the schools.
  • Contact strategies: the investigators will show a video of a young male who had been diagnosed (i.e., not an actor) with depression.

Benefits:

* The intervention group will join educational intervention program they expected to benefit from the program through increase their depression literacy and improve depression stigma, and control group will not join any form of intervention.

Risk: There is no expected risk for participating in the study.

Consent: Three Informed Consents forms will be signed from students, guardians and school manager.

Study Overview

Study Type

Interventional

Enrollment (Actual)

360

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

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

10 years to 19 years (Child, Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Students needed to be enrolled in one of the selected schools during the academic year 2015-2016.
  • Must be in the age group 10-19 years.
  • Must agree to participate in the study (consent was obtained from the students,and proxy consent was obtained from guardians).

Exclusion Criteria There were no exclusion criteria for participation in this study.

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 Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control group
No intervention
Experimental: Intervention group
they will be enrolled in an educational program and video contact.
Educational strategies: 2 Lecture about depression 30 minutes supported by group discussion, brochures and display of posters with mental-health slogans on depression in the schools.
Contact strategies: Investigators will show a video of a young male who had been diagnosed with depression. The video presented information that was moderately disconfirming of prior stereotypes by balancing the individual's difficulties resulting from Depression, with his ability to live a normal life.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Depression Literacy measured by Depression Literacy Questionnaire (D-Lit)
Time Frame: is measured at baseline, directly after the intervention and three months follow-up.
is measured by Depression Literacy Questionnaire (D-Lit)
is measured at baseline, directly after the intervention and three months follow-up.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Depression Stigma measured by Depression Stigma Scale (DSS)
Time Frame: is measured at baseline, directly after the intervention and three months follow-up.
is measured by Depression Stigma Scale (DSS)
is measured at baseline, directly after the intervention and three months follow-up.
Change in Depression Self-Stigma measured by Self Stigma of Depression Scale (SSDS)
Time Frame: is measured at baseline, directly after the intervention and three months follow-up.
is measured by Self Stigma of Depression Scale (SSDS)
is measured at baseline, directly after the intervention and three months follow-up.

Collaborators and Investigators

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

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)

January 1, 2016

Primary Completion (Actual)

April 1, 2016

Study Completion (Actual)

April 1, 2016

Study Registration Dates

First Submitted

January 19, 2016

First Submitted That Met QC Criteria

January 25, 2016

First Posted (Estimate)

January 26, 2016

Study Record Updates

Last Update Posted (Actual)

October 28, 2020

Last Update Submitted That Met QC Criteria

October 25, 2020

Last Verified

October 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • U1111-1179-1857

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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