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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04404621
Other study ID # 2000026437
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 13, 2019
Est. completion date September 12, 2020

Study information

Verified date June 2021
Source Yale University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to investigate and compare how 18-weeks of computer-based brain training and physical exercise together can improve physical performance, cognitive function and mood in older adults in a cross-over design with participants randomized to receive the intervention first and then be assessed before and after an 18 week period without intervention, or the reverse sequence.


Description:

The aim of this study is to investigate and compare how 18-weeks of computer-based brain training and physical exercise together can improve physical performance, cognitive function and mood in older adults in a cross-over design with participants randomized to receive the intervention first and then be assessed before and after an 18 week period without intervention, or the reverse sequence. 80 adults between the ages of 65 and 105 years old will be invited to participate. After providing informed consent, in the case of subjects who are living on units for individuals with memory or other cognitive compromise, after assent from the individual and approval from facility staff, subjects will be randomly assigned to either receive the intervention for 18 weeks and then be followed for an additional 18 weeks, or to be followed for 18 weeks without intervention and then do the intervention for 18 weeks. The intervention will consist of 18 weeks of 60-minute PE sessions 3-4 times/week and 25-minute CBB training sessions 3-4 times a week. There will be 3 assessments of participants: before and after the first 18-week period and then again after the second 18-week period. Assessments will be done in 2 sessions over a total of 90 minutes and will include demographic, health, physical activity and social activity questionnaires as well as the self-report measures of cognitive function, emotional state and weekly activities; quantitative assessments of physical balance, strength, flexibility blood pressure and heart rate; and tests of cognitive function. Subject medications will be recorded at each assessment. The wait-list control group will receive the same assessments at the same time points.


Recruitment information / eligibility

Status Completed
Enrollment 34
Est. completion date September 12, 2020
Est. primary completion date September 12, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: - Associated with Whitney center as residents or participants in non-resident programs. - Able to understand and read English. Exclusion Criteria: - Not able to sit in a chair independently. - Not able to move both arms in simple movement sequence. - Hearing and vision insufficient to do the computer exercises or follow the PE instructions. - Not able to remember 3 movements in succession.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Physical exercise (PE) training and computer-based brain (CBB)
18 weeks of PE and CBB.

Locations

Country Name City State
United States Connecticut Mental Health Center New Haven Connecticut

Sponsors (1)

Lead Sponsor Collaborator
Yale University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Composite cognition score Composite from: Flanker Test of Attention; Go/No-Go Test of Response Inhibition; List Sort Working Memory Test; Logical Memory Story Recall; Digit symbol coding; Digit Span Forwards and Backwards; Hopkin's Verbal Learning Test; Trail Making B; Stroop Color Word; Category Verbal Fluency; Reaction Time.
A composite score will be calculated for each participant at baseline and after training and waitlist periods by first determining Z-scores for each test for each participant at each time point based on means and standard deviations for the entire sample at baseline, and then averaging the individual's Z-scores at that time point.
18 weeks
Primary Sit to Stand in one-minute Number of times able to go from sit to stand in in one minute 18 weeks
Primary Balance - stand on one foot at a time Stand on one foot with the toe of the other foot touching the calf of the standing leg - number of seconds able to maintain. The sum of right and leg foot will be added. 18 weeks
Primary Mood and Quality of Life Composite score from WHODAS, DEMQ QLI and Beck Depression Inventory.
A composite score will be calculated for each participant at baseline and after training and waitlist periods by first determining Z-scores for total score on each questionnaire for each participant at each time point based on means and standard deviations for the entire sample at baseline, and then averaging the individual's Z-scores at that time point.
18 weeks
Secondary Attention and Speed of Processing Flanker Test of Attention (average reaction time on correct incongruent trials) 18 weeks
Secondary Response Inhibition Percent correct on no-go trials on Go/No-Go Test 18 weeks
Secondary Working Memory Average z-scores on two tests of working memory: 1)List Sorting Working Memory (total score which is the sum of scores on parts one and two) and Digit Span (sum of longest span forward and longest span backwards) 18 weeks
Secondary Verbal Memory Logical Memory Story Recall (number of details correctly recalled on initial recall) 18 weeks
Secondary Speed of Processing Digit Symbol Coding (number of correct responses in 60 seconds) 18 weeks
Secondary Cognitive Flexibility Color/Word Stroop Test (Time to read words in conflicting colors minus time to read words without conflicting colors 18 weeks
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