Acquired Brain Injury Clinical Trial
Official title:
Functional Outcomes Following Neuropsychological Intervention in Acquired Brain Injury Outpatients With Executive Dysfunction
NCT number | NCT01992055 |
Other study ID # | H2013:389 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | December 2013 |
Est. completion date | March 2017 |
Verified date | April 2019 |
Source | University of Manitoba |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This Clinical Trial is a pilot study being conducted to study the impact of a specific
cognitive rehabilitation program, Goal Management Training (GMT), in adult patients with
executive dysfunction and associated problems in everyday functioning. The intervention
program will also include relaxation training and psychoeducation regarding brain injury on
everyday functioning, emotional status, and executive functioning. Goal Management Training
focuses on teaching individuals strategies to compensate for executive functioning deficits
and is based on a theory of goal neglect resulting in disorganized behavior following frontal
lobe injury. It emphasizes strategies for self-monitoring and self-evaluation in everyday
life. Given its goal-oriented emphasis, focus on individual everyday difficulties, and
reports of improvements in self-reported executive failures and mood, GMT appears to be an
ideal intervention treatment for individuals with executive and functional deficits.
Given the emphasis of goal-oriented rehabilitation on reducing the impact of cognitive
impairment on daily functioning, rather than attempting to restore cognitive abilities, a
reduction in subjective reports of psychological distress is anticipated. This hypothesis is
consistent with existing literature revealing reduced reports of annoyance and executive
difficulties on self-report inventories. Improvements on tests of sustained attention and
visuospatial problem-solving, as well as small effects on additional measures of planning,
are also anticipated.
Status | Completed |
Enrollment | 18 |
Est. completion date | March 2017 |
Est. primary completion date | March 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Participants may be included in the study if they are identified as having EF impairments, secondary to an acquired brain injury, and are between the ages of 18 and 65 years. Informed consent will be gathered from each participant. Eligible participants will be informed about the purpose of the study, the associated risks and benefits, and their option to withdraw from the study at any time without penalty. Potential risks include subtle discomfort when initially participating in relaxation exercises, which typically resolves with familiarity, and mild distress during neuropsychological assessment. These issues sometimes arise during standard clinical practice and the neuropsychologists involved are experienced in assisting people in reducing their distress. Exclusion Criteria: - Individuals with significant memory impairment, receptive language deficits, active psychosis, severe depression (i.e., Beck Depression Inventory - II [BDI-II] = 30), or a diagnosis of dementia will be excluded from participating in the study.. A minimum of 36 participants will be recruited for this study. |
Country | Name | City | State |
---|---|---|---|
Canada | University of Manitoba | Winnipeg | Manitoba |
Lead Sponsor | Collaborator |
---|---|
University of Manitoba | Health Sciences Centre Foundation, Manitoba |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Change from Baseline in neuropsychological functioning at 1 year post-intervention | Change in test scores on the following measures: Connor's Continuous Performance Test - II Delis-Kaplan Executive Functioning Scale Tower Test Trail Making Test Ruff Figural Fluency Test Controlled Oral Word Association Test Semantic Fluency Golden's Stroop Color and Word Test BADS Six Elements Test Brief-A Self and Family Report Inventories SCL-90-R Self-Report Inventory Word Memory Test Medical Symptom Validity Test Non-Verbal MSVT |
1 year post intervention | |
Primary | Change from Baseline in neuropsychological functioning at 1 week post-intervention | Change in test scores on the following measures: Connor's Continuous Performance Test - II Delis-Kaplan Executive Functioning Scale Tower Test Trail Making Test Ruff Figural Fluency Test Controlled Oral Word Association Test Semantic Fluency Golden's Stroop Color and Word Test BADS Six Elements Test Brief-A Self and Family Report Inventories SCL-90-R Self-Report Inventory Word Memory Test Medical Symptom Validity Test (MSVT) Non-Verbal MSVT |
1 week post-intervention | |
Secondary | Change from Baseline in neuropsychological functioning at 4 weeks post-intervention | Change in test scores on the following measures: Connor's Continuous Performance Test - II Delis-Kaplan Executive Functioning Scale Tower Test Trail Making Test Ruff Figural Fluency Test Controlled Oral Word Association Test Semantic Fluency Golden's Stroop Color and Word Test BADS Six Elements Test Brief-A Self and Family Report Inventories SCL-90-R Self-Report Inventory Word Memory Test Medical Symptom Validity Test Non-Verbal MSVT |
4 weeks post-intervention |
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