- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03514004
Using Information and Communication Technologies to Prevent Suicide in Chile
Using Information and Communication Technologies to Prevent Suicide Among Secondary School Students in Two Regions of Chile: a Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
There is increasing concern regarding adolescent suicide in Latin America. Recent mental health policies foster the development and implementation of preventive interventions for suicide. Such initiatives, however, have been scarcely developed, even in countries with solid mental health services, such as Chile. The use of information and communication technologies (ICT) might contribute to create accessible, engaging, and innovative platforms to promote well-being and support for adolescents with mental health needs and suicide risk. Promising evidence from high-income countries has already shown the potential benefits of ICT-based programs but further research is needed, especially in settings with restrained resources. Providing local evidence is crucial for persuading policy makers and other stakeholders, and it will prove crucial in order to widely disseminate and scale up the program, if it is found to be effective.
A cluster randomized controlled trial (RCT) to evaluate an ICT-based program will be conducted to prevent suicide and enhance mental health among adolescents in Chile. Four-hundred high-school students will be recruited from 6 public schools in two regions of Chile. Study procedures will be as follows: 1) design of the intervention model and creation of prototype; 2) selection and randomization of the participating schools; 3) implementation of the 3-month intervention and evaluation at baseline, post-intervention period, and a 2-month follow-up.
The ICT-based program utilizes a web-based platform and a mobile application to cultivate a virtual community to promote mental health protective factors, such as self-esteem and self-expression, and prevent adolescent suicide. To overcome the frequent barriers to help seeking, the program will provide rapid direct access to quality, evidence-based information and real-time assistance from a mental health professional; encourage habits that improve emotional and physical health; facilitate self-monitoring of mental health and personal progress; and promote social integration and participation in community-based activities. The program is based on the principles of peer support and inclusivity, and as such, its name is "Project Clan," in reference to a diverse group of individuals who come together for a common purpose in a welcoming environment. The privacy and anonymity of each "Clan member" will be respected, so that they feel free to openly express themselves and resolve questions about possibly taboo topics related to mental health and suicide. Project Clan includes both informational and interactive features, ranging from traditional suicide prevention strategies (e.g., a chat with a psychologist, emergency phone hotline, and tips) that seek to reduce barriers to access quality, useful, and evidence-based information and rapid professional assistance; to components designed to increase interactions between participants and promote a sense of belonging and connection with the other Clan members.
Suicidal ideation is the primary outcome in this study. Secondary outcomes include negative psychological outcomes (e.g., stigma, depression, anxiety) as well as a number of protective psychological and social factors. Indicators regarding the study implementation process will be also gathered. Pertinent study documents (e.g., research protocol, instruments, informed consent, and informed assent forms) were approved by the Ethics Committee for Human Subjects Research of the Faculty of Medicine, Universidad de Chile.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Students who attend participating public high schools in two cities (Santiago and Rancagua) of Chile
Exclusion Criteria:
- Students having visual or physical impairments that are incompatible with the intervention model
- Student having a prior diagnosis of a mental disorder.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention
The ICT-based intervention is known as "Project Clan."
Each participant randomized to the intervention group will have access to the web platform and mobile applications of "Project Clan" - a virtual community that seeks to promote adolescent mental health and wellbeing as students interact, express themselves, and resolve concerns, with the support of peers and mental health professionals.
During the three-month intervention, participants will have complete anonymity, unless trained psychologists supervising the platform as "community counselors" identify behaviors associated with suicide risk and proceed to follow an established emergency protocol.
The counselors will be available to answer community questions and provide support on an individual basis.
|
The ICT-based intervention, known as "Project Clan," includes both a web-platform and a mobile application.
Project Clan includes both informational and interactive features, ranging from traditional suicide prevention strategies (e.g., a chat with a psychologist, emergency phone hotline, and tips) that seek to reduce barriers to access quality, useful, and evidence-based information and rapid professional assistance, to components designed to increase interactions between participants and promote a sense of belonging and connection with the other "Clan" members.
Other Names:
|
|
No Intervention: Control
Participants in the control group will also be assigned a username and password to access the website, but they will be met with a user interface that only displays a space to answer the corresponding assessments.
In addition to the introductory presentation, they will be given a brochure with information regarding adolescent suicide and wellbeing and tips with regard to seeking help and assisting others.
This will include the contact information for a telephone hotline, to ensure they can receive professional help if needed.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Okasha Suicidality Questionnaire
Time Frame: change from baseline suicidality at 5-month follow up
|
Self-administered instrument exploring suicidal ideation and beliefs about suicide.
Previously linked to suicide intent, depression, despair, low-self-esteem, impulsivity, and low social support.
Item is sensitive to identifying immediate risk for suicide attempt.
4 items (scale 0-3; scale range= 0-12).
|
change from baseline suicidality at 5-month follow up
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Coopersmith Self- Esteem Inventory
Time Frame: change from baseline self-esteem at 5-month follow up
|
Self-report scale on self-esteem among youth and adolescents in personal and social contexts.
58 items (scale 0-1).
|
change from baseline self-esteem at 5-month follow up
|
|
Barratt Impulsiveness Scale
Time Frame: change from baseline impulsiveness at 5-month follow up
|
Self-report scale assessing cognitive, motor, and not planned impulsivity.
30 items (scale 0-4).
|
change from baseline impulsiveness at 5-month follow up
|
|
General Self-Efficacy Scale
Time Frame: change from baseline self-efficacy at 5-month follow up
|
Self-report scale assessing self-efficacy among youth across a number of daily stressors.
10 items (scale 1-3).
|
change from baseline self-efficacy at 5-month follow up
|
|
Coping Across Situations Questionnaire
Time Frame: change from baseline coping at 5-month follow up
|
Self-report scale assessing stress coping strategies among youth.
16 items.
(scale 1-5).
|
change from baseline coping at 5-month follow up
|
|
Perceived Social Support Scale
Time Frame: change from baseline perceived social support at 5-month follow up
|
Self-report scale assessing emotional help and advice among youth.
12 items (scale 1-5)
|
change from baseline perceived social support at 5-month follow up
|
|
Social Skills Scale
Time Frame: change from baseline social skills at 5-month follow up
|
Self-report scale assessing social skills through self-expression of anger or compliance in different scenarios.
33 items (scale 1-4).
|
change from baseline social skills at 5-month follow up
|
|
Depression Anxiety Stress scales
Time Frame: change from baseline anxiety-depression-stress at 5-month follow up
|
Self-report scale assessing depression, anxiety, and stress symptoms.
21 items (scale 0-3).
|
change from baseline anxiety-depression-stress at 5-month follow up
|
|
Discrimination and Devaluation Scale
Time Frame: change from baseline discrimination-devaluation at 5-month follow up
|
Self-report scale assessing awareness of stereotyping attitudes towards mental illness (12 items) (scale 0-3).
|
change from baseline discrimination-devaluation at 5-month follow up
|
Collaborators and Investigators
Sponsor
Collaborators
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- ID16I10060
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Given our commitment to the relevancy of this study, we agree to:
- Register this study at ClinicalTrials.gov. This record will be updated at least every 12 months, as required.
- Report aggregate results no later than one year after the clinical trial completion date, in a publication.
Furthermore, the University of Chile (UCH) has an internal policy to ensure that clinical trials comply with University and sponsor policy and regulatory standards.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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