One-year Patient Reported Outcomes Following Hospitalization for Trauma

Terminated

• Conditions: Wounds and Injuries

• Registration Number: NCT02909231
• Lead Sponsor: University of Calgary

Brief Summary

This study evaluates the three, six, and twelve month patient reported outcomes of people admitted two trauma centres in western Canada over a four month period. Participants are evaluated using the Trauma Outcome Profile and a custom survey instrument.

Detailed Description

This study intends to assess patient reported outcomes following discharge from trauma services at the Foothills Medical Centre (FMC) and Vancouver General Hospital (VGH). The investigators will survey participants with pen-and-paper surveys at three, six and twelve months following discharge from hospital. The survey instrument being used is the Trauma Outcomes Profile, which has been previously validated in this population, supplemented by a supplemental survey to help further describe resources this population has access to in their recovery. The results of these surveys will be compared with pre-injury health status, injury types, mechanisms, and discharge medications and treatments. The investigators anticipate enrolling 500 participants starting in October 2016. At the conclusion of the study the investigators will have a better understanding of patient reported functional outcomes after trauma and will be better positioned to design trauma rehabilitation systems to service this population.

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2016-09
• Study First Submitted: 2016-09-19
• Study First Submitted QC: 2016-09-19
• Study First Posted: 2016-09-21
• Status Verified: 2017-12
• Primary Completion: 2017-12-05
• Study Completion: 2017-12-05
• Last Update Submitted: 2017-12-05
• Last Update Posted: 2017-12-07

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 42

Inclusion Criteria

• admitted to the trauma service at VGH or FMC
• Age 18 or older
• resident of Canada

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Exclusion Criteria

• English language literacy
• Impairments in cognition, motor, or communication that limit the ability to complete a paper-based survey
• No fixed address

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Medium-term health-related quality of life	Up to one year	Assessment at 3, 6 and 12 months using the Trauma Outcomes Profile survey instrument.

Secondary Outcome Measures

Name	Time	Method
Local resource use for trauma patients admitted to hospital	Up to one year	Assessment at 3, 6, and 12 months using a custom survey to assess local resource use and perceived needs

Trial Locations

Locations (2)

Foothills Medical Centre; 🇨🇦 Calgary, Alberta, Canada

Vancouver General Hospital; 🇨🇦 Vancouver, British Columbia, Canada