Yoga for Seniors

May 12, 2021 updated by: University of Wisconsin, Madison
The overall purpose of this study is to deliver a 12-week yoga program to older adults (over 60 years of age) in rural WI who do not have access to yoga programming and examine the effects of the programming on activities of daily living, gait, balance, falls, activity level and social isolation.

Study Overview

Detailed Description

Participants will be assigned to immediately begin a 12-week yoga class (2 classes per week for 75 minutes each) or complete a 12-week wait (wait-list control). The measures of interest will be examined at pretest (wait-list only), baseline, posttest and at 3-month follow-up to see what, if any, changes are maintained after completion of the program. All assessment data collections sessions will be conducted on-site at a predetermined site identified by the community partners.

Study Type

Interventional

Enrollment (Actual)

88

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

    • Wisconsin
      • Madison, Wisconsin, United States, 53706
        • University of Wisconsin

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 and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Ability to independently ambulate for at least 10 minutes continuously (with or without an assistive device)
  • Ability to attend the yoga class for all or most of the 12 weeks
  • A previous fall, near-fall or identified fear of falling

Exclusion Criteria:

  • No known contraindication for exercise (i.e. a medical doctor has told you not to exercise)
  • A resent injury that causes pain during movement
  • Current enrollment in another research study or class focused on balance

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: Prevention
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Yoga Program
12-week yoga program begins immediately
free 12 week yoga program, twice a week for 75 minutes each
Garmin VivoSmart activity monitor throughout study
Active Comparator: Wait-list Control
Wait-listed to take the Yoga Program in 12-weeks time
Garmin VivoSmart activity monitor throughout study
assigned to take the Yoga Program in 12-weeks

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in MiniBESTest Score
Time Frame: [pre-test for waitlist group 3 months prior to class], baseline, post-test (3-months), 3-month follow up (6-months)
The mini-BESTest will be used to assess balance. This 14-item, clinical battery is used to assess balance in four component areas (anticipatory transitions, postural response, sensory orientation and dynamic gait) and provides a single number summary of balance performance. Scores range from 0 to 28, with higher scores indicating higher function.
[pre-test for waitlist group 3 months prior to class], baseline, post-test (3-months), 3-month follow up (6-months)
Change in Fall Frequency
Time Frame: [pre-test for waitlist group 3 months prior to class], baseline, post-test (3-months), 3-month follow up (6-months)
Change in the frequency of falls will be assessed using a forced-choice paradigm: none, once, 2 to 10 times, weekly, or daily over the last 6 months.
[pre-test for waitlist group 3 months prior to class], baseline, post-test (3-months), 3-month follow up (6-months)
Change in the Canadian Occupational Performance Measures (COPM)
Time Frame: [pre-test for waitlist group 3 months prior to class], baseline, post-test (3-months), 3-month follow up (6-months)
The COPM is composed of the following steps: 1) participant identifies occupational performance problems for self-care and productivity, 2) participant rates each issue on a score of 1-10 (higher scores are more important), 3) participant chooses 5 most important problems, 4) participant rates each issue (1-10) for performance and satisfaction, 5) average score for each (performance and satisfaction) are calculated. Final score for each is 1-10 with higher scores better.
[pre-test for waitlist group 3 months prior to class], baseline, post-test (3-months), 3-month follow up (6-months)
Change in Activities-Specific Balance Confidence Scale (ABC)
Time Frame: [pre-test for waitlist group 3 months prior to class], baseline, post-test (3-months), 3-month follow up (6-months)
The ABC Scale measures a fear of falling. It is a 16-item survey where participants rate their level of self-confidence (0-100, where 100 is the highest self-confidence) for each item. The average score is reported.
[pre-test for waitlist group 3 months prior to class], baseline, post-test (3-months), 3-month follow up (6-months)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Standardized Gait Analysis: Gait Velocity
Time Frame: [pre-test for waitlist group 3 months prior to class], baseline, post-test (3-months), 3-month follow up (6-months)
Using the GaitRite® System, the temporal and spatial parameters of each participant will be captured during walking. The GaitRite® mat is a 14 foot portable electronic walkway, embedded with sensors to enable the measurement spatiotemporal variables of gait such as cadence, normalized velocity, stride length, base of support, and percent of cycle in double support. Participants will begin at a starting point two meters from the mat, then walk toward and step onto the mat to continue walking until they achieve the stop line located two meters off of the opposite side of the mat. Data will be collected for forward preferred speed, backward preferred speed, forward fast, tandem and dual task gait. Each participant will complete five trials for each condition.
[pre-test for waitlist group 3 months prior to class], baseline, post-test (3-months), 3-month follow up (6-months)

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Activity Level Measured by Number of Steps Taken
Time Frame: [pre-test for waitlist group 3 months prior to class], baseline, post-test (3-months), 3-month follow up (6-months)
Participants will be fitted with a Garmin VivoSmart activity monitor and will be asked to wear the device for the duration of the study.
[pre-test for waitlist group 3 months prior to class], baseline, post-test (3-months), 3-month follow up (6-months)
Change in Performance Assessment of Self-Care Skills (PASS)
Time Frame: [pre-test for waitlist group 3 months prior to class], baseline, post-test (3-months), 3-month follow up (6-months)
The Performance Assessment of Self-Care Skills (PASS) assesses basic self-care and instrumental activities of daily living. Subscales: Independence, Safety, and Adequacy (0-3 where higher scores indicate less difficulty with basic self-care).
[pre-test for waitlist group 3 months prior to class], baseline, post-test (3-months), 3-month follow up (6-months)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Kristen A Pickett, PhD, University of Wisconsin, Madison

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)

May 30, 2019

Primary Completion (Actual)

February 24, 2020

Study Completion (Actual)

February 24, 2020

Study Registration Dates

First Submitted

May 12, 2021

First Submitted That Met QC Criteria

May 12, 2021

First Posted (Actual)

May 17, 2021

Study Record Updates

Last Update Posted (Actual)

May 17, 2021

Last Update Submitted That Met QC Criteria

May 12, 2021

Last Verified

May 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • 2019-0479
  • A176000 (Other Identifier: UW Madison)
  • EDUC/KINESIOLOGY (Other Identifier: UW Madison)

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.

Clinical Trials on Aging Well

Clinical Trials on Yoga Program Immediately

Subscribe