- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04889131
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
Status
Terminated
Conditions
Intervention / Treatment
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.
Sponsor
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.
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