MedPath

Early Intervention Following Mild TBI

Not Applicable
Completed
Conditions
Mild Traumatic Brain Injury
Registration Number
NCT01947504
Lead Sponsor
Elaine De Guise
Brief Summary

The objective of the study is to implement and measure the efficiency of a standardized acute and brief non-pharmacological intervention (Cognitive interventions on Sleep - Anxiety - Attention - Memory) following mild TBI and observe their impact pre- and post-treatments. The ultimate goal is to have patients be re-integrated to their activities faster with lesser symptoms and have patients present lesser post-concussive symptoms. Specific objectives: 1) Measure the effect of an acute and brief non-pharmacological intervention on PCS symptoms, sleep, headaches, affect, cognition and functional outcome following mild TBI; 2)To redefine a model of outcome prediction following mild TBI.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Clinical diagnosis of Mild TBI
Exclusion Criteria
  • Psychiatric diagnosis

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Recurrence of post-concussive symptoms1 year
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

McGill University Health Center

🇨🇦

Montreal, Quebec, Canada

McGill University Health Center
🇨🇦Montreal, Quebec, Canada

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.