MedPath

Enhancing Cognitive Control Abilities Using Mobile Technology in a Senior Living Community

Not Applicable
Terminated
Conditions
Aging
Cognitive Change
Registration Number
NCT04905849
Lead Sponsor
University of California, San Francisco
Brief Summary

The goal of this study is to test the feasibility of launching a personalized digital health assessment and remediation program for the older adults in senior living communities based upon an initial characterization of these abilities. Evidence of feasibility here using these unique methodological approaches would provide empirical evidence supporting the basis for a larger-scale implementation of such digital health technologies into less controlled senior settings.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
12
Inclusion Criteria
  • Must be living at a Senior Living Community
  • have own iPad and/or smartphone,
  • native-English speaker.

Participation across a spectrum of cognitive abilities is desired for this study, specifically for older adults in a community setting.

Exclusion Criteria
  • Do not have any physical or cognitive limitations that would clearly prevent them from utilizing these applications as intended

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Primary Outcome Measures
NameTimeMethod
Number of Participants Who Attempted to Complete the Adaptive Cognitive Evaluation (ACE) From Baseline at 6 WeeksAt Baseline and post intervention at the 6 week mark

ACE is a custom mobile cognitive health assessment battery that presents paradigms typically used in standard cognitive neuroscience laboratories. Here the investigators will assess a measure of (1) Attention and (2) Working memory in the ACE software.

Secondary Outcome Measures
NameTimeMethod
Mean Performance on the Everyday Cognition Scale (ECog) From Baseline at 6 WeeksAt Baseline and post intervention at the 6 week mark

The Everyday Cognition Scale (ECog) measures the ability to perform everyday tasks that demand memory, language, visuospatial abilities, planning, organization, and divided attention. The ECog consists of a global and domain scores for each of the previously described categories, and is scored as follows: 1= better or no change compared to 10 years earlier, 2= questionable/occasionally worse compared to 10 years earlier, 3= consistently a little worse compared to 10 years earlier, 4= consistently much worse compared to 10 years earlier. Thus, the lower the overall score is on this measure at both the global and domain score level, the better one is performing with respect to their cognition.

Mean Change on Cognitive Failures Questionnaire (CFQ) From Baseline at 6 WeeksAt Baseline and post intervention at the 6 week mark

The Cognitive Failures Questionnaire (CFQ) assesses participant distractibility. The CFQ score ranges from 0 to 100, with the lower the overall score is on this measure, the better one is performing with respect to their cognition.

Mean Change on General Health and Well-being (SF-36) From Baseline at 6 WeeksAt Baseline and post intervention at the 6 week mark

The general health and well-being (SF-36) score assesses participant health. The SF-36 score ranges from 0 to 100. The higher the overall score is on this measure, the better one is performing with respect to their health and well-being.

Trial Locations

Locations (1)

UC San Francisco

🇺🇸

San Francisco, California, United States

UC San Francisco
🇺🇸San Francisco, California, United States

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