Clinical Trials Directory

Trials / Completed

CompletedNCT02711085

Modeling Post-traumatic Pain and Recovery: The SYMBIOME Longitudinal Cohort Study

The Systematic Merging of Biology, Mental Health and Environment (SYMBIOME) Longitudinal Databanking Project

Status
Completed
Phase
Study type
Observational
Enrollment
134 (actual)
Sponsor
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study will explore the contribution of stress-system activity to pain and functional disability in the acute stage of traumatic musculoskeletal injury, and to the maintenance of symptoms after 3, 6 and 12 months post-injury.

Detailed description

Purpose: The purpose of this protocol is to establish a longitudinal database of data collected from people having experienced an acute traumatic injury to their musculoskeletal system. This includes injuries commonly considered 'non-catastrophic' or 'minor' soft tissue injuries such as whiplash, low back injuries, sports or slip and fall-type injuries that result in sprain/strain of muscle, tendon, ligament or other such soft tissues. Uncomplicated bony fractures (those that are managed through casting only, non-surgical) will also comprise this cohort. The data will include biological specimens, psychological and cognitive profiles, and social/environmental indicators. This protocol represents the start of the SYStematic Merging of Biology, Mental health and Environment (SYMBIOME) project from the emerging Solving Traumatic pain and disability through Advanced Research Translation (START) research group centred at Western. Over time, this database will allow rich exploration of complex interactions between biology, psychology and environment as they relate to the resolution of traumatic pain and disability, or similarly the persistence thereof. Additional research ethics board (REB) applications will be submitted as those projects are ready to be formally conducted.

Conditions

Interventions

TypeNameDescription
OTHERNo interventionNo intervention - observational study

Timeline

Start date
2015-12-01
Primary completion
2020-12-01
Completion
2020-12-01
First posted
2016-03-17
Last updated
2021-08-12

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT02711085. Inclusion in this directory is not an endorsement.