- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05097690
Case Control Psychological Autopsy of Suicide
October 16, 2021 updated by: Tamkeen Saleem
Psychological Autopsy: An Investigation to Explore Antecedents, Sequelae and Causes of Case Control Suicide Equivocal Behavior
Suicide is a leading cause of death worldwide, and identifying risk factors has been considered as the key initiative of suicide prevention.
Considering that, the study aimed to explore the factors leading towards suicide in Pakistan through Case-Control Psychological Autopsy of Suicide.
Also, the study aimed to Translate, Adapt and Validate American Association of Suicidology (AAS) Semi-Structured Interview for Psychological Autopsy (Generic Version, 2018).
Study Overview
Status
Enrolling by invitation
Conditions
Study Type
Observational
Enrollment (Anticipated)
50
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
-
-
Capital
-
Islamabad, Capital, Pakistan, 44000
- International Islamic University, Islamabad Pakistan
-
-
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 35 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Cases are those individuals who died by suicide and the controls include individuals who survive after attempting suicide.
Description
Inclusion Criteria:
- The age of the deceased by suicide and living controls will range from 10 to 35 years.
- The key informants will be of 18 years of age and above without any learning
- disability.
- The key informants will be a close family member or immediate friend.
- Only suicides took place in 2019 to September 2021.
Exclusion Criteria:
- If contact was deemed to pose a risk to the safety of the researcher (likely intoxication; history of or potential for violence).
- Informants who are not willing to give written informed consent will be excluded from the study.
- Informants who are taking any psychological help in the past and present will be excluded from the 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
- Observational Models: Case-Control
- Time Perspectives: Retrospective
Cohorts and Interventions
Group / Cohort |
---|
Case
Case (Fatal Suicide)
|
Control
Control (Non-Fatal Suicidal Behavior)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The Semi-structured Interview for Psychological Autopsy
Time Frame: Upto 6 months
|
American Association of Suicidology Semi-Structured Interview for Psychological Autopsy
|
Upto 6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Dr Tamkeen Saleem, PhD, International Islamic University, Islamabad, Pakistan
- Study Chair: Dr Michelle O'Reilly, PhD, University of Leicester and Leicestershire Partnership NHS Trust
- Study Chair: Dr Domenico Giacco, PhD, Warwick Medical School, University of Warwick
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)
October 14, 2021
Primary Completion (Anticipated)
February 25, 2022
Study Completion (Anticipated)
March 30, 2022
Study Registration Dates
First Submitted
September 25, 2021
First Submitted That Met QC Criteria
October 16, 2021
First Posted (Actual)
October 28, 2021
Study Record Updates
Last Update Posted (Actual)
October 28, 2021
Last Update Submitted That Met QC Criteria
October 16, 2021
Last Verified
October 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AAS-ATV-PAS
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
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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