- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03219424
Predicting the Probability of Return To Work After Injury
Predicting the Probability of Return to Work After Injury in Hong Kong: Prospective Multicentre Cohort Study
Study Overview
Status
Conditions
Detailed Description
Background:
Trauma is a leading cause not only of death worldwide but also of disability, and in Hong Kong it ranks sixth as a cause of death for all age groups. The implementation of trauma systems has improved the survival of injured patients in many settings including Hong Kong. However, the aim of trauma care for the injured person is not only to prolong life but also to restore patients to the best possible health status, and where applicable, to return to work. Survivors of trauma often experience late sequelae that have a major impact on almost all aspects of everyday life, and improvements in functional outcome and health status may continue for at least five years post-injury.
Objectives:
- to evaluate return to work (RTW) status after moderate and major trauma in Hong Kong at one year after injury;
- to derive reliable prediction models for RTW.
Study design:
This is a multi-centre, prospective long-term follow up cohort study of the 1163 trauma patients admitted to the Prince of Wales Hospital (PWH), Queen Elizabeth Hospital (QEH) and Tuen Mun Hospital (TMH) in Hong Kong in 2017-2018. Patients will be recruited within four weeks of ED attendance as soon as the patient is clinically stable and conscious. The follow-up period for return to work status of the 1163 trauma patients will extend from baseline to one year after trauma.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
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NT
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Sha Tin, NT, Hong Kong
- Prince of Wales Hospital
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Aged 18 years or above
- Eligible for the trauma registry
- Working or seeking employment before injury
Exclusion Criteria:
- Isolated hip or pathological fractures
- Injury severity score (ISS) of 1
- Patients who are unwilling to enter the study
- Patients who have left Hong Kong
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Return to work status at 12 months after injury
Time Frame: 12 months after injury
|
The proportion of trauma patients who return to work at 12 months after injury
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12 months after injury
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change of Glasgow Outcome Scale-Extended (GOSE) over time
Time Frame: On admission, 30 days after injury, 3 months after injury, 6 months after injury, 9 month after injury and 12 months after injury
|
Change of GOSE over time
|
On admission, 30 days after injury, 3 months after injury, 6 months after injury, 9 month after injury and 12 months after injury
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- CREC2016.667-T
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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