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Ottawa Suicide Prevention in Men Pilot Study

NCT02718248 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 7

Last updated 2018-08-20

Study results available
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Summary

To refine a novel intervention using a combination of a smart phone application with best practice psychotherapy for men who have presented to hospital with intentional self-harm. The outcome will be change in baseline of scores on a depression rating scale the PHQ-9 at six weeks. Moreover, the investigators will ask participants about the acceptability of the intervention and the acceptability of using routine data sources as outcome measures. This will inform methods of recruitment for the larger cluster randomized controlled trial and the creation of a treatment manual.

Conditions

  • Suicide

Interventions

DEVICE

CHESS Mobile Health smart phone application

A smart phone application designed to reduce intentional self-harm through problem solving e-therapy.

BEHAVIORAL

Problem solving therapy

Face to face problem solving therapy every week for six weeks.

Sponsors & Collaborators

  • University of Ottawa

    lead OTHER

Principal Investigators

  • Simon Hatcher, MD, PhD · University of Ottawa

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-09-30
Primary Completion
2017-04-30
Completion
2017-06-30

Countries

  • Canada

Study Locations

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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 NCT02718248 on ClinicalTrials.gov