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A Feasibility Study of a Suicide Prevention Video

NCT05119946 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2021-11-15

No results posted yet for this study

Summary

This initial study is a pilot feasibility study with a primary objective of assessing the feasibility of a larger study by evaluating the procedures and methodology, as well as collecting pilot data. The eventual research goal is to demonstrate whether a suicide prevention video in addition to standard care for suicidality is an effective strategy to reduce suicidal behaviours in individuals with a history of such. The suicide prevention video is developed as an educational tool to inform participants of the various consequences of suicide as well as giving a message of hope. It is hoped that such an approach will help to reduce future suicidal behaviours in those who have a history of such. If so, then this could be made as a part of the standard of care in treating patients with suicidality.

Conditions

Interventions

BEHAVIORAL

Suicide prevention video

The video has been developed by the research team as an educational tool to teach patients about suicide, the consequences of such and imparting a message of hope.

OTHER

Standard suicide treatment

The standard suicide treatment will be determine by the attending physician and can include medications and/or psychotherapy

Sponsors & Collaborators

  • Fraser Health

    lead OTHER

Principal Investigators

  • Hem Phaterpekar, MD · Fraser Health

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-01-31
Primary Completion
2020-06-30
Completion
2020-06-30

Countries

  • Canada

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05119946 on ClinicalTrials.gov