A Smartphone Intervention With Telemedicine Support for Management of Post-traumatic Stress Disorder: A Randomized Trial

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

67 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-12-31

Study Completion Date

2017-04-30

Brief Summary

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This study tests whether people receiving clinician support to use a mobile application on their smartphone can manage their post-traumatic stress disorder (PTSD) symptoms better than those who do not. Half of the participants will receive the clinician supported smartphone application intervention and the other half will remain on the waiting list.

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Detailed Description

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Conditions

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PostTraumatic Stress Disorder

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Waiting list control

Group Type NO_INTERVENTION

No interventions assigned to this group

Intervention

Clinician-supported smartphone application intervention

Group Type EXPERIMENTAL

Clinician supported smartphone application intervention

Intervention Type OTHER

Interventions

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Clinician supported smartphone application intervention

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* on the waiting list for the Ontario Shores traumatic stress clinic;
* score ≥ 31 on the PCL-5
* have access to a smartphone or tablet to which they are willing to download the app.