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Post-Traumatic Brain Injury (Post-TBI) Fatigue and Its Treatment

Primary Purpose

Fatigue

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Modafinil
Placebo
Sponsored by
Icahn School of Medicine at Mount Sinai
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fatigue focused on measuring Fatigue, TBI, brain injury, Modafinil, traumatic brain injury

Eligibility Criteria

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

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.

Sites / Locations

  • Icahn School of Medicine at Mount Sinai

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Modafinil

Placebo

Arm Description

single dose of 200 mg. a day of modafinil for four weeks

Outcomes

Primary Outcome Measures

Fatigue
Self-report of fatigue

Secondary Outcome Measures

Cognitive Performance
Cognitive performance
Mood
mood
Pain
pain
Sleep Quality
sleep quality
Health Status
health status
Participation
participation
Quality of Life
quality of life

Full Information

First Posted
October 3, 2005
Last Updated
March 16, 2016
Sponsor
Icahn School of Medicine at Mount Sinai
Collaborators
U.S. Department of Education
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1. Study Identification

Unique Protocol Identification Number
NCT00233090
Brief Title
Post-Traumatic Brain Injury (Post-TBI) Fatigue and Its Treatment
Official Title
Post-TBI Fatigue and Its Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
March 2016
Overall Recruitment Status
Terminated
Why Stopped
Insufficient recruitment
Study Start Date
July 2005 (undefined)
Primary Completion Date
December 2008 (Actual)
Study Completion Date
December 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Icahn School of Medicine at Mount Sinai
Collaborators
U.S. Department of Education

4. Oversight

5. Study Description

Brief Summary
Randomized clinical trial of modafinil vs. placebo for treatment of fatigue after TBI.
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 function, 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fatigue
Keywords
Fatigue, TBI, brain injury, Modafinil, traumatic brain injury

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
21 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Modafinil
Arm Type
Experimental
Arm Description
single dose of 200 mg. a day of modafinil for four weeks
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Modafinil
Intervention Description
single dose of 200 mg. a day of modafinil for four weeks
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
daily dose of placebo for four weeks.
Primary Outcome Measure Information:
Title
Fatigue
Description
Self-report of fatigue
Time Frame
comparison pre and post treatment
Secondary Outcome Measure Information:
Title
Cognitive Performance
Description
Cognitive performance
Time Frame
comparison pre and post treatment
Title
Mood
Description
mood
Time Frame
comparison pre and post treatment
Title
Pain
Description
pain
Time Frame
comparison pre and post treatment
Title
Sleep Quality
Description
sleep quality
Time Frame
comparison pre and post treatment
Title
Health Status
Description
health status
Time Frame
comparison pre and post treatment
Title
Participation
Description
participation
Time Frame
comparison pre and post treatment
Title
Quality of Life
Description
quality of life
Time Frame
comparison pre and post treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility 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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wayne A Gordon, Ph.D.
Organizational Affiliation
Icahn School of Medicine at Mount Sinai
Official's Role
Principal Investigator
Facility Information:
Facility Name
Icahn School of Medicine at Mount Sinai
City
New York
State/Province
New York
ZIP/Postal Code
10029-6574
Country
United States

12. IPD Sharing Statement

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Post-Traumatic Brain Injury (Post-TBI) Fatigue and Its Treatment

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