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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03058055
Other study ID # BEST
Secondary ID
Status Completed
Phase N/A
First received February 12, 2017
Last updated December 17, 2017
Start date July 15, 2016
Est. completion date December 15, 2017

Study information

Verified date December 2017
Source University of Kentucky
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The BEST study will investigate the feasibility of cognitive interventions in a randomized, placebo-controlled, clinical trial. The investigators will recruit 45 cognitively normal subjects and engage them in one of three cohorts over an 8 week period, including active reading vs. origami study arms and a placebo group without structured cognitive intervention.


Description:

This is a randomized, placebo controlled study investigating the practical implementation and conduct of two cognitive interventions in non-demented subjects. Subjects will be randomized 1:1:1 into three groups including: 1) a Book club that includes weekly one hour meetings and daily reading assignments, 2) Origami lessons (one hour/week) with daily take home Origami activities to complete, and 3) a placebo group with unstructured lifestyle activities (normal lifestyle activities without restraint).


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date December 15, 2017
Est. primary completion date December 15, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria:

- Non demented community dwelling elders

Exclusion Criteria:

- Unable to perform the reading or origami tasks for any reason

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Placebo
The placebo group will have unstructured lifestyle activities (normal lifestyle activities without restraint).
Origami
Origami lessons (one hour/week) with daily take home Origami activities to complete
Reading
Book club that includes weekly one hour meetings and daily reading assignments

Locations

Country Name City State
United States Sander's Brown Center on Aging Lexington Kentucky

Sponsors (1)

Lead Sponsor Collaborator
University of Kentucky

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary MOCA The Montreal Cognitive Assessment (MOCA) measures general cognitive function 8 weeks
Primary FCSRT The Free and Cued Selective Reminding Test (FCSRT) measures memory function. 8 weeks
Secondary Adherence to protocol Objective measures of weekly time devoted to cognitive training activities 8 weeks
Secondary Electroencephalogram resting state electroencephalogram pattern 8 weeks
Secondary Evoked Related Potential Evoked Related Potential P300 using the Bluegrass memory task 8 weeks
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