Cognitive Function Clinical Trial
Official title:
Promoting Mental Acuity in Elderly Populations Through Incentive for Technology Use
Verified date | December 2013 |
Source | Carnegie Mellon University |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Federal Government |
Study type | Interventional |
In this between-subject randomized controlled trial the investigators will test the impact of three novel structured financial incentives: atomistic, altruistic and team-based. These incentive schemes will be used to motivate one month of daily use of software designed to improve cognitive function (including memory, reaction times, attention and executive function) among the elderly. The 400 participants will be members of retirement communities in Pennsylvania. Three outcomes will be monitored and analyzed: activities completed using the software (primary), performance on the activities, and changes in cognitive functioning. This study is designed to be a pilot study. The investigators will have 90% power to find a mean daily difference of 4 activities completed in the control group versus 7 activities completed in the incentive groups assuming a standard deviation of 3.5 and an alpha of 0.017 (the bonferroni corrected significance level to account for multiple comparisons). In addition during a three month "follow-up period" all participants will have continued access to the software, however, no incentives will be provided for use. This period will be used to assess the impact of the initial incentives on long run use after financial incentives have ceased.
Status | Completed |
Enrollment | 312 |
Est. completion date | May 2011 |
Est. primary completion date | May 2011 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 55 Years to 85 Years |
Eligibility |
Inclusion Criteria: - Age between 55 and 85 - Resident in participating retirement community Exclusion Criteria: - Unstable medical conditions that would likely prevent the subject from completing the study - Severe depression - Inability to read or severe cognitive deficits that would preclude ability to read consent form or fill out surveys |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | Retirement communities near Pittsburgh Pennsylvania | Pittsburgh | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
Carnegie Mellon University | National Institute on Aging (NIA), Pennsylvania Department of Health |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Daily activities completed | 4 months | No | |
Secondary | Performance on completed activities | 4 months | No |
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