Ignite Creation Date:
2024-05-05 @ 9:29 PM
Last Modification Date:
2024-10-26 @ 10:04 AM
Study NCT ID:
NCT00893347
Status:
COMPLETED
Last Update Posted:
2018-11-06
First Post:
2009-05-04
Brief Title:
An Intervention Program to Reduce to the Risk of Persistent Symptoms After Concussion
Sponsor:
University of British Columbia
Organization:
University of British Columbia
Study Overview
Official Title:
Prevention of Persistent Post-concussion Syndrome With Cognitive-behavioural Therapy in At-risk Patients
Status:
COMPLETED
Status Verified Date:
2012-11
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study investigates how well a new therapy program prevents persistent symptoms eg headaches fatigue irritability etc after concussion The program involves examining beliefs about concussion and learning healthy coping strategies and is completed with the first three months post-injury
Detailed Description:
Although the majority of patients with mild traumatic brain injury MTBI experience complete recovery within three months a sizeable group continues to report frequent and severe symptoms such as headaches fatigue difficulty concentrating forgetfulness and irritability in what is labeled persistent post-concussion syndrome PCS Persistent PCS is associated with vocational recreational and social disability Early education and reassurance treatment as usual is effective in general but appears insufficient for this subgroup
Recent research has identified risk factors for persistent PCS including inaccurate illness beliefs maladaptive coping behaviour and emotional distress The present study will evaluate the additive efficacy of a cognitive-behavioural therapy protocol designed to modify these risk factors over and above treatment as usual
Participants with MTBI will be recruited within six weeks of injury Those identified as being at-risk for persistent PCS based on evidence-based criteria will receive treatment as usual and then be randomly assigned to receive either no further intervention or cognitive-behavioural therapy We hypothesize that the group receiving cognitive-behavioural therapy will have fewer PCS symptoms and be less disabled at follow-up We also hypothesize that compensation-seeking status will mitigate this improvement and that illness beliefs coping behaviour and emotional distress will mediate this improvement A blinded rater will conduct the baseline and outcome assessments
Recent research has identified risk factors for persistent PCS including inaccurate illness beliefs maladaptive coping behaviour and emotional distress The present study will evaluate the additive efficacy of a cognitive-behavioural therapy protocol designed to modify these risk factors over and above treatment as usual
Participants with MTBI will be recruited within six weeks of injury Those identified as being at-risk for persistent PCS based on evidence-based criteria will receive treatment as usual and then be randomly assigned to receive either no further intervention or cognitive-behavioural therapy We hypothesize that the group receiving cognitive-behavioural therapy will have fewer PCS symptoms and be less disabled at follow-up We also hypothesize that compensation-seeking status will mitigate this improvement and that illness beliefs coping behaviour and emotional distress will mediate this improvement A blinded rater will conduct the baseline and outcome assessments
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None