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

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.

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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