Parkinson's Disease Clinical Trial
Official title:
A Randomized Controlled Trial of Neurocognitive and Supportive Therapy Interventions for Individuals With Parkinson's Disease
This randomized, controlled trial (RCT) evaluates the benefits of memory and problem solving
training compared to supportive therapy in individuals with Parkinson's Disease with Mild
Cognitive Impairment (MCI) and their support persons. Participants will be randomly assigned
to receive memory and problem solving training or supportive therapy for 2-months. A 6-month
follow up evaluation will establish if benefits remain over time. Impact of these therapies
on thinking abilities, physical health, and patient and support person ratings of thinking
skills, mood and quality of life will be evaluated. The memory and problem solving training
is hypothesized to result in greater improvements and/or stability of function on
neuropsychological tests of attention, working memory, learning, and memory skills compared
to the supportive therapy condition. Both conditions are hypothesized to result in improved
mood and quality of life ratings.
Results from this study will determine whether memory and problem solving therapies and
supportive therapy are easily used by and beneficial for individuals with Parkinson's
Disease and Mild Cognitive Impairment. If positive benefit is observed, information from
this study will be used to further optimize these therapies for larger trials designed to
evaluate the value of the therapies for individuals with Parkinson's Disease and their
support persons.
Status | Completed |
Enrollment | 32 |
Est. completion date | December 2015 |
Est. primary completion date | October 2015 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Clinical diagnosis of Parkinson's Disease - Clinical diagnosis of Mild Cognitive Impairment Exclusion Criteria: - Clinical diagnosis of Dementia - Clinical diagnosis of other Parkinson's Disease-associated comorbid conditions (e.g., severe anxiety, depression, excessive daytime sleepiness, or psychosis) that significantly influence cognitive testing |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | VCU Parkinson's and Movement Disorders Center | Richmond | Virginia |
Lead Sponsor | Collaborator |
---|---|
Virginia Commonwealth University | Michael J. Fox Foundation for Parkinson's Research |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | California Verbal Learning Test-II Long Delay Free Recall Scaled Score Change Over 6 Months | Change in California Verbal Learning Test-II Long Delay Free Recall Scaled Score from Baseline and 6 months | Change from Baseline in California Verbal Learning Test-II Long Delay Free Recall Scaled Score at 6 months | No |
Other | Linear Analog Scale Assessment Overall Well Being Raw Score Change Over 6 Months | Change in Linear Analog Scale Assessment Overall Well Being Raw Score from Baseline and 6 months | Change from Baseline in Linear Analog Scale Assessment Overall Well Being Raw Score at 6 months | No |
Primary | California Verbal Learning Test-II Long Delay Free Recall Scaled Score Change Over 10 Weeks | Change in California Verbal Learning Test-II Long Delay Free Recall Scaled Score from Baseline and 10 weeks | Change from Baseline in California Verbal Learning Test-II Long Delay Free Recall Scaled Score at 10 weeks | No |
Secondary | Linear Analog Scale Assessment Overall Well Being Raw Score Change Over 10 Weeks | Change in Linear Analog Scale Assessment Overall Well Being Raw Score from Baseline and 10 weeks | Change from Baseline in Linear Analog Scale Assessment Overall Well Being Raw Score at 10 weeks | No |
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