- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03799640
Multidirectional Yoga for Cognition
September 9, 2019 updated by: Joseph Signorile, University of Miami
Multidirectional Yoga Training to Improve in Healthy Older Participants
Older individuals, 60-90, will be provided regular or cognitively based yoga training.
They will then be evaluated using standard cognitive testing devices.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
Reductions in executive function are common with age.
Along with these declines come reductions in simple functional patterns of daily living such as crossing a street, walking in a crowded area, or performing any functions that occurs in an open (changing) environment.
This study will use a newly developed yoga program incorporating multi-directional movements, cognitive challenges and visuomotor disturbances to improve executive function and associated movements in persons over 60 years of age.
Study Type
Interventional
Enrollment (Actual)
40
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Florida
-
Coral Gables, Florida, United States, 33147
- Laboratory of Neruomuscular Research and Active Aging
-
Coral Gables, Florida, United States, 33146-2416
- Max Orovitz Laboratories
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
60 years to 90 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- 60-90 years of age
- Capable of walking 50 feet with or without a walking aid-
Exclusion Criteria:
- Regularly participating in yoga or other balance training program
- Currently participating in another exercise study
- Unable to commit to study duration
- Uncontrolled neuromuscular or cardiovascular disease that prevents participation in an exercise study
- Advised not to exercise by their physician
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Standard Yoga
Yoga will be performed using linear forward and backward movements.
|
The multidirectional yoga training program will use both simple and complex movement sequences (asana or postures) that include a cognitive component.
For example, participants will be taught a movement sequence that includes 16-20 yoga postures that increase in difficulty as the training progresses.
Lectures on health and fitness
|
|
Experimental: Multi-directional Yoga
The multidirectional yoga training program will use both simple and complex movement sequences (asana or postures) that include a cognitive component.
For example, participants will be taught a movement sequence that includes 16-20 yoga postures that increase in difficulty as the training progresses. .
|
Lectures on health and fitness
Yoga using standard poses and linear movements
|
|
Experimental: Educational Control
Lectures on Health and Wellness
|
The multidirectional yoga training program will use both simple and complex movement sequences (asana or postures) that include a cognitive component.
For example, participants will be taught a movement sequence that includes 16-20 yoga postures that increase in difficulty as the training progresses.
Yoga using standard poses and linear movements
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
NIH Toolbox: Picture Sequence Memory Test
Time Frame: 5 minutes
|
Measures episodic memory.
Participants are asked to reproduce a sequence of pictures that is shown on the screen.
|
5 minutes
|
|
NIH Toolbox Flanker test
Time Frame: 5 minutes
|
Measures attention and inhibitory control.
Participant focuses on a given stimulus while inhibiting attention to stimuli flanking it.
|
5 minutes
|
|
NIH Toolbox List Sorting test
Time Frame: 5 minutes
|
Measures working memory.
Participant recalls and sequences different visually and orally presented stimuli.
|
5 minutes
|
|
NIH Toolbox Pattern Comparison Processing Speed test
Time Frame: 5 minutes
|
Measures speed of processing.
Participants discern whether two side-by-side pictures are the same or not, with 85 seconds to respond to as many items as possible.
Items are simple so as to purely measure processing speed.
|
5 minutes
|
|
Walking Executive Function Tests
Time Frame: 10 minutes
|
Walking and responding to visual cues presented on a 60 inch monitor.
|
10 minutes
|
|
Timed up-and-go
Time Frame: 5 minutes
|
Rising from a chair, circumventing a cone and returning to the chair.
|
5 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 5, 2018
Primary Completion (Actual)
August 15, 2019
Study Completion (Actual)
August 15, 2019
Study Registration Dates
First Submitted
January 8, 2019
First Submitted That Met QC Criteria
January 8, 2019
First Posted (Actual)
January 10, 2019
Study Record Updates
Last Update Posted (Actual)
September 10, 2019
Last Update Submitted That Met QC Criteria
September 9, 2019
Last Verified
September 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- 20180704
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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