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Depression and Traumatic Brain Injury

Primary Purpose

Depression, Traumatic Brain Injury

Status
Completed
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
citalopram (celexa)
Sponsored by
Sunnybrook Health Sciences Centre
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depression focused on measuring depression, traumatic brain injury, serotonin transporter, genetic polymorphisms, citalopram

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: age >18 years gender: male or female TBI within the last two months mild to moderate TBI written, informed consent depressed group only: diagnosis of major depressive episode using the depression module of the Structured Clinical Interview for the DSM-IV (SCID-IV) Exclusion Criteria: prior TBI or other focal brain disease (stroke, tumor) significant acute medical illness, including: drug overdose, severely disturbed liver, kidney, lung, or heart function, anemia, hypothyroidism, uncontrolled diabetes, Parkinson's disease, Huntington's chorea, progressive supranuclear paralysis, brain tumor, subdural hematoma, multiple sclerosis a brain CT scan revealing focal lesions that could not be interpreted as consistent with a TBI depression group only: contraindications to receiving treatment with citalopram

Sites / Locations

  • Sunnybrook Health Sciences Centre

Outcomes

Primary Outcome Measures

- Hamilton Depression Rating Scale (HAM-D)

Secondary Outcome Measures

Beck Depression Inventory (BDI), Rivermead Head Injury Follow-up Questionnaire (RHFQ), General Health Questionnaire (GHQ), Rivermead Post Concussion Disorder Questionnaire (RPDQ)

Full Information

First Posted
November 10, 2005
Last Updated
April 26, 2017
Sponsor
Sunnybrook Health Sciences Centre
Collaborators
Ontario Mental Health Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT00254007
Brief Title
Depression and Traumatic Brain Injury
Official Title
The Serotonin Transporter Gene Polymorphism and Major Depression Following Traumatic Brain Injury
Study Type
Interventional

2. Study Status

Record Verification Date
April 2017
Overall Recruitment Status
Completed
Study Start Date
July 2003 (undefined)
Primary Completion Date
December 2005 (Actual)
Study Completion Date
May 2010 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Sunnybrook Health Sciences Centre
Collaborators
Ontario Mental Health Foundation

4. Oversight

5. Study Description

Brief Summary
Problem: Depressive symptoms are a common mental health problem following traumatic brain injury (TBI), occurring in up to 87% of patients. Depression following TBI has important consequences including poor functioning, lack of ability to return to work and family activities and prolonged TBI symptoms. The reason depression develops in some patients following TBI is unknown, making treatment difficult. One type of brain protein that shows genetic differences between people is called the serotonin transporter. People can be divided by whether or not they have a short protein (S allele) or a long protein (L allele) which influences the amount of serotonin transporter. Serotonin is a key brain chemical in depression in many mental/psychiatric illnesses. We think that the genetic differences in the serotonin transporter, that may not make a difference before TBI, may become important after TBI due to the nature of these injuries. Methods: A consecutive sample of 200 patients attending a TBI clinic who have sustained a mild-to-moderate TBI (American Congress of Rehabilitation Medicine criteria) within the last 2 months will be assessed for the presence of major depression (standard criteria, standardized interview). In phase I, blood samples from patients with mild-to-moderate TBI with depression and without depression will be checked for the presence of the 5-HTTPR genetic difference. This will allow us to study if the S allele is more likely in TBI patients with depression. In phase II, the patients with depression will be treated with the SSRI citalopram for 6 weeks. At 6 weeks, or upon discontinuation of citalopram, depression will be assessed again. This will allow us to study if depressed patients with the S allele respond more poorly to treatment. Persons assessing depression after treatment will not know the genetic makeup of each patient. Results Expected: If the serotonin transporter genetic difference confers susceptibility to depression following TBI, this will provide important information on what causes depression following TBI and document a risk factor for depression previously unstudied in this population. Also, as SSRI antidepressants are used to treat depression in TBI, this study may identify a subgroup of TBI patients in whom different medications should be given or additional medications are required.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Traumatic Brain Injury
Keywords
depression, traumatic brain injury, serotonin transporter, genetic polymorphisms, citalopram

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
citalopram (celexa)
Intervention Description
20(1 tablet)-50(2 1/2 tablets) mg/day for a period of 6 or 10 weeks
Primary Outcome Measure Information:
Title
- Hamilton Depression Rating Scale (HAM-D)
Time Frame
Baseline, 6 weeks and 10 weeks (if applicable)
Secondary Outcome Measure Information:
Title
Beck Depression Inventory (BDI), Rivermead Head Injury Follow-up Questionnaire (RHFQ), General Health Questionnaire (GHQ), Rivermead Post Concussion Disorder Questionnaire (RPDQ)
Time Frame
Baseline, 6 weeks and 10 weeks (if applicable)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age >18 years gender: male or female TBI within the last two months mild to moderate TBI written, informed consent depressed group only: diagnosis of major depressive episode using the depression module of the Structured Clinical Interview for the DSM-IV (SCID-IV) Exclusion Criteria: prior TBI or other focal brain disease (stroke, tumor) significant acute medical illness, including: drug overdose, severely disturbed liver, kidney, lung, or heart function, anemia, hypothyroidism, uncontrolled diabetes, Parkinson's disease, Huntington's chorea, progressive supranuclear paralysis, brain tumor, subdural hematoma, multiple sclerosis a brain CT scan revealing focal lesions that could not be interpreted as consistent with a TBI depression group only: contraindications to receiving treatment with citalopram
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Krista L Lanctot, PhD
Organizational Affiliation
Sunnybrook Health Sciences Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sunnybrook Health Sciences Centre
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M4N 3M5
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
18465388
Citation
Chan F, Lanctot KL, Feinstein A, Herrmann N, Strauss J, Sicard T, Kennedy JL, McCullagh S, Rapoport MJ. The serotonin transporter polymorphisms and major depression following traumatic brain injury. Brain Inj. 2008 Jun;22(6):471-9. doi: 10.1080/02699050802084886.
Results Reference
result

Learn more about this trial

Depression and Traumatic Brain Injury

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