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Post-TBI Fatigue and Its Treatment
This study is currently recruiting participants.
Verified by Mount Sinai School of Medicine, October 2007
Sponsors and Collaborators: Mount Sinai School of Medicine
National Institute of Disability and Rehabilitation Research
Information provided by: Mount Sinai School of Medicine
ClinicalTrials.gov Identifier: NCT00233090
  Purpose

Randomized clinical trail of modafinil vs. placebo for treatment of fatigue after TBI.


Condition Intervention Phase
Fatigue
Drug: Modafinil
Phase IV

Drug Information available for: Modafinil
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study
Official Title: Post-TBI Fatigue and Its Treatment

Further study details as provided by Mount Sinai School of Medicine:

Primary Outcome Measures:
  • Self-report of fatigue

Secondary Outcome Measures:
  • Cognitive performance
  • mood
  • pain
  • sleep quality
  • health status
  • participation
  • quality of life

Estimated Enrollment: 112
Study Start Date: July 2005
Estimated Study Completion Date: October 2008
Detailed Description:

Purpose: The purpose of this study is to examine the efficacy of the drug modafinil as a treatment for fatigue post TBI.

Background: After TBI, fatigue is one of the most common complaints, as documented in our work and that of many other researchers. People with TBI experience fatigue that seems to them out of proportion to whatever work they are doing or effort they are making. Fatigue after TBI is associated with decreased participation in normal activities in the community and has been linked to depression.

Need for Research: Research on use of drugs to treat post-TBI fatigue is inadequate. While studies of fatigue in people with other chronic conditions suggest that modafinil helps relieve fatigue and has fewer side effects than some other drugs used in treating fatigue, the use of modafinil has not yet been tested in people with TBI.

Current and Future Research Activity: More than 100 men and women volunteers who complain of post-TBI fatigue will be randomly assigned to a 4-week period of taking modafinil or a placebo. At the beginning and end of the study, the severity of their fatigue and associated symptoms (e.g., cognitive fucniton, mood, pain, daytime sleepiness, sleep quality, health status) will be assessed, as well as their participation in activities and perceived quality of life. It is hypothesized that modafinil will reduce the symptoms of fatigue and will increase level of activity and perceived quality of life to a significantly greater extent than will the placebo.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

- Individuals who sustained a TBI with a documented loss of consciousness or evidence of a TBI on neuroimaging studies and who are at least 12 months post-injury, who complain of fatigue and who have scores of 22 or above on the Barroso Fatigue Scale will be eligible to participate in this study. Subjects must not meet criteria for alcohol or substance abuse using the Structured Clinical Interview for DSM-IV (SCID) for at least six months prior to study enrollment.

Exclusion Criteria:

- diagnosis of chronic neurological disease (including Lyme disease), narcolepsy, current infectious disease, chronic fatigue syndrome, fibromyalgia, anemia, hypothyroidism not adequately controlled with medication, blood pressure greater 150/100 mm Hg, or clinically significant major systemic disease. In addition, individuals taking medications which are known to cause fatigue will be excluded from participation in the study.

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00233090

Contacts
Contact: Wayne A Gordon, Ph.D. wayne.gordon@mssm.edu

Locations
United States, New York
Mount Sinai School of Medicine Recruiting
New York, New York, United States, 10029-6574
Contact: Wayne A Gordon, Ph.D.         wayne.gordon@mssm.edu    
Sponsors and Collaborators
Mount Sinai School of Medicine
National Institute of Disability and Rehabilitation Research
Investigators
Principal Investigator: Wayne A Gordon, Ph.D. Mount Sinai School of Medicine
  More Information

study website  This link exits the ClinicalTrials.gov site

Study ID Numbers: 02-0677, H133A020501
Study First Received: October 3, 2005
Last Updated: October 18, 2007
ClinicalTrials.gov Identifier: NCT00233090  
Health Authority: United States: Institutional Review Board

Keywords provided by Mount Sinai School of Medicine:
Fatigue
TBI
brain injury
Modafinil
traumatic brain injury

Study placed in the following topic categories:
Signs and Symptoms
Fatigue
Brain Injuries
Modafinil

Additional relevant MeSH terms:
Therapeutic Uses
Physiological Effects of Drugs
Central Nervous System Stimulants
Protective Agents
Neuroprotective Agents
Central Nervous System Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 16, 2009