Evaluation of a Website to Improve Depression Literacy in Parents of Adolescents With Depression

Sponsor
Ludwig-Maximilians - University of Munich (Other)
Overall Status
Completed
CT.gov ID
NCT05335564
Collaborator
Prof. OTTO Beisheim Stiftung (Germany) (Other)
33
1
1
15.3
2.2

Study Details

Study Description

Brief Summary

The aim of this study is to evaluate the efficacy and acceptability of the website "ich bin alles" (https://www.ich-bin-alles.de/) to improve depression literacy (knowledge about depression, which aid the recognition, treatment or prevention of depression) in parents of adolescents with acute or remitted depressive disorder. The investigators will examine whether the website improves depression literacy in parents of adolescents aged 12 to 18 years with a history of depression. The investigators will also assess the acceptability of the website among the participants.

Condition or Disease Intervention/Treatment Phase
  • Other: General information about depression
N/A

Detailed Description

Few young people with major depressive disorder seek professional treatment in time. Concerns about social stigma, confidentiality, and limited knowledge about mental health conditions, such as depression, or mental health services are some of the main barriers to seek treatment. Increasing parents' knowledge about and attitude towards depression and mental health in childhood and adolescence is important to increase parents' awareness towards their children's mental health and reduce possible prejudices and barriers towards depression and treatment. These aspects might contribute to more parents seeking professional help and treatment for their children at an early point of time in the course of a depressive disorder. To address these issues and contribute to knowledge gain, we developed an evidence-based website "ich bin alles" (https://www.ich-bin-alles.de/) with two separate sub-websites for (1) adolescents and (2) parents to improve depression literacy in these groups.

To improve depression literacy in parents, the website provides general information for parents about depression in childhood and adolescence (e.g., symptoms, causes, course and treatment of depression). Furthermore, the website provides information about strategies for parents on how to support their children if they are affected by depression and on appropriate prevention strategies; i.e., strategies for promoting mental health (e.g., providing a healthy environment, reducing stress, undertaking positive activities, positive parenting), which are meant to serve as an addition to professional treatments of depression or to promote mental health in adolescents.

Target groups of the website are parents of adolescents aged 12 to 18 years with a history of depression, as well as parents of healthy adolescents aged 12 to 18 years. Easy access to information about depression would make early recognition of depression more likely and engage parents to help their children to seek help for depression.

Since the website targets two different groups, the investigators will evaluate the website accordingly:

Target group 1: Parents of adolescents with a major depressive disorder (acute or remitted) Target group 2: Parents of healthy adolescents (without a mental health condition)

The current study will focus on target group 1. A study focusing on target group 2 can be found in a separately registered clinical trial on clinicaltrials.gov.

The primary aim of this study is to evaluate the efficacy and acceptability of the website "ich bin alles" (https://www.ich-bin-alles.de/) to improve depression literacy in parents of adolescents with acute or remitted depressive disorder.

Study Design

Study Type:
Interventional
Actual Enrollment :
33 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Evaluating the Efficacy and the Acceptability of the Website "Ich Bin Alles" to Improve Depression Literacy in Parents of Adolescents With Acute or Remitted Major Depressive Disorder
Actual Study Start Date :
Jan 20, 2021
Actual Primary Completion Date :
May 2, 2022
Actual Study Completion Date :
May 2, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: General information about depression

Exposure to general information about depression

Other: General information about depression
Before starting the intervention, the participants are told that they will be shown parts of a website about depression. The participants are instructed to carefully attend to the website (e.g., to read the text precisely, to hear attentively to the podcasts and to view carefully the videos and images on the website). The time window spent for the reception of each part of the website are fixed. The participants will be shown parts of the website regarding general information about depression.

Outcome Measures

Primary Outcome Measures

  1. Change in Depression Literacy - Depression in children and adolescents as psychiatric disorder [Pre-Test, Post-Test (within 2 hours), Follow-Up (Week 4)]

    This self-designed questionnaire is a self-report inventory to assess knowledge of depression in children and adolescents (frequency and comorbidities, treatment, symptoms, causes and course of depression; 26 items), with higher scores indicating more knowledge of depression as psychiatric disorder. Participants will complete this self-designed questionnaire at pre-test, post-test and follow-up to determine change in knowledge of depression in children and adolescents.

Secondary Outcome Measures

  1. Visual Aesthetics of Websites Inventory Short Version (VisAWI-S) [Post-Test (within 2 hours)]

    The short version of the Visual Aesthetics of Websites Inventory (VisAWI-S) is self-report inventory to assess the evaluation of the website's design - especially the perceived visual aesthetics. Participants indicate their response to the four items (e.g., "The layout appears professionally designed") on a seven-point Likert scale (ranging from 1 "do not agree at all" to 7 "do fully agree").

  2. Overall reception of the website [Post-Test (within 2 hours)]

    The overall reception of the website as measured with a self-designed questionnaire.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • The presence of a current or remitted diagnosis of a mild, moderate, or severe major depressive episode according to ICD-10 Criteria: F32.0; F32.1; F32.2, F33.0, F33.1, F33.2) in the participants' children is assessed using a semi-structured clinical interview: the "Kinder-DIPS". The Kinder-DIPS is a well-established German interview for the diagnosis of a wide range of axis I psychiatric disorders in children from ages six to 18.
Exclusion Criteria:
  • Insufficient knowledge of German

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital Munich Munich Bayern Germany 80336

Sponsors and Collaborators

  • Ludwig-Maximilians - University of Munich
  • Prof. OTTO Beisheim Stiftung (Germany)

Investigators

  • Study Director: Gerd Schulte-Körne, Professor, Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital Munich

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ellen Greimel, Working group leader, Ludwig-Maximilians - University of Munich
ClinicalTrials.gov Identifier:
NCT05335564
Other Study ID Numbers:
  • 20116_1
First Posted:
Apr 19, 2022
Last Update Posted:
Jun 30, 2022
Last Verified:
Jun 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ellen Greimel, Working group leader, Ludwig-Maximilians - University of Munich
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 30, 2022