Mild Cognitive Impairment Clinical Trial
Official title:
Cognitive Screening and Cognitive Training in Seniors
| NCT number | NCT02588209 |
| Other study ID # | RGK11-52 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | January 2012 |
| Est. completion date | December 2017 |
| Verified date | October 2023 |
| Source | The University of Texas at Dallas |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
This study will provide cognitive screenings for seniors age 50 and older. It will also investigate the benefits of two different cognitive training programs for seniors who have lower baseline performance on memory and/or gist reasoning tests.
| Status | Completed |
| Enrollment | 71 |
| Est. completion date | December 2017 |
| Est. primary completion date | June 2015 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 50 Years to 80 Years |
| Eligibility | Inclusion Criteria: - Cognitive complaints in the absence of dementia - Participate in tasks involving motor abilities such as use of at least one arm and hand - Read, speak, and comprehend English - At least 50 years of age - Comprehend simple instructions, perform tasks, and take part in intervention Exclusion Criteria: - Not proficient in reading,comprehending, and speaking English - History of learning disability, stroke, cognitive impairment, major psychiatric illness, alcoholism, or substance abuse |
| Country | Name | City | State |
|---|---|---|---|
| United States | UTD Center for BrainHealth | Dallas | Texas |
| Lead Sponsor | Collaborator |
|---|---|
| The University of Texas at Dallas |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Improvement in memory or thinking after brain training | To examine short-term effects of treatment on cognition using neuropsychological measures | beginning (0 weeks) to end (4 weeks) | |
| Secondary | Measures changes in brain wave activity | Electrophysiological responses will be recorded using event related potential to monitor responses to yes/no stimuli. | beginning (0 weeks) and end (4 weeks) |
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