- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05287529
In-home Yoga for Seniors
Telehealth Delivery of the Yoga for Seniors Program
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Participants will be randomly assigned to immediately begin an 8-week yoga class or complete an 8-week wait (wait-list control). Investigators will examine the measures of interest at pretest (wait-list only), baseline, and posttest to see what, if any, changes are observed after completion of the program. All assessment data collections sessions will be conducted on-line.
Phone screen: All interested participants will complete a phone screen to assess inclusion and exclusion factor for the study.
Testing Procedures: All participants who meet study requirements will complete approximately 60 to 90 minutes of on-line assessments and 60-90 minutes of mailed questionnaires at each testing timepoint (pretest, baseline, and posttest). The assessments will consist of demographic information including a health history form, a semi-structured interview, and a series of questionnaires. The following are the specific assessment components for each time point:
A. Intake and review of forms (Initial Visit (Baseline or Pretest ))
- Consent form
- Medical history
B. Clinical measures (all visits)
- Current medication list
- Falls history and fear of falls questionnaire
- Canadian Occupational Performance Measure
- Physical Activity Scale
- Perceived Stress Scale
- Loneliness and Social Isolation Scales
- Social Network Scale
C. Barriers and facilitators assessments (all visits)
- technology use assessment survey
- physical activity readiness scale
D. Exit evaluation (posttest only)
All selected assessment tools have been previously investigated and are valid and reliable for their described use.
During the initial visit (pretest or baseline), participants will complete components A-C listed above.
Individuals in the wait-list control group will complete components B and C during their baseline visit (prior to starting yoga, following their 8-week wait)
Posttest assessment Components B-D will be completed at posttest. Posttest data will be collected within 10 days of the participant's last day of the yoga class.
The group that starts immediately will have 2 time-points of data collection (pretest, posttest), the waitlisted group will have 3 time-points of data collection (baseline, pretest, posttest). Individual results will not be shown or discussed with participants.
The yoga program is an in-home, chair-assisted yoga class focused on balance. Each class will be led by a certified yoga teacher who has completed training the the yoga for Seniors Program. Classes will consist of no more than 12 participants. Each class will be attended by a local community member who will facilitate community building before and after class and will be available to activate local emergency medical services in the unlikely event that the need arises. Classes are 75 minutes in duration and meet two times per week.
See also 12-week program called Yoga for Seniors registered to NCT04889131
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Wisconsin
-
Madison, Wisconsin, United States, 53706
- University of Wisconsin
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- over 60 years of age
- 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 8 weeks
- a previous fall, near-fall or identified fear of falling
- internet access
- vision at or corrected to 20/40 or better
Exclusion Criteria:
- known contraindication for exercise (i.e. a medical doctor has told you not to exercise)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: PREVENTION
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: 8-Week Yoga Class
Randomized to immediately begin an 8-week Yoga Class via Telehealth
|
The yoga program is an in-home, chair-assisted yoga class focused on balance.
Each class will be led by a certified yoga teacher who has completed training the the yoga for Seniors Program.
Classes will consist of no more than 12 participants.
Each class will be attended by a local community member who will facilitate community building before and after class and will be available to activate local emergency medical services in the unlikely event that the need arises.
Classes are 75 minutes in duration and meet two times per week.
|
|
ACTIVE_COMPARATOR: Waitlisted for 8-Week Yoga Class
Randomized to start an 8-week Yoga Class via Telehealth 8-weeks from the start of the study.
|
The yoga program is an in-home, chair-assisted yoga class focused on balance.
Each class will be led by a certified yoga teacher who has completed training the the yoga for Seniors Program.
Classes will consist of no more than 12 participants.
Each class will be attended by a local community member who will facilitate community building before and after class and will be available to activate local emergency medical services in the unlikely event that the need arises.
Classes are 75 minutes in duration and meet two times per week.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Percentage of Classes Attended (?0
Time Frame: up to 8 weeks
|
Participant adherence will be measured in part by class attendance. They will have twice weekly classes for 8 weeks, or 16 possible classes to attend. [from the purpose: The overall purpose of this study is to adapt the 12-week, standardized in-home yoga program into an 8-week in-home program with a high degree of fidelity, participant adherence, and safety. Are fidelity/adherence/safety a primary outcomes?] |
up to 8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Fall Frequency
Time Frame: baseline (or pretest for immediate group), 8 weeks (posttest for immediate group, pretest for waitlist group), 16 weeks (posttest for waitlist group)
|
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 2 weeks, 1 month, and 6 months.
|
baseline (or pretest for immediate group), 8 weeks (posttest for immediate group, pretest for waitlist group), 16 weeks (posttest for waitlist group)
|
|
Change in Activities-Specific Balance Confidence Scale (ABC)
Time Frame: baseline (or pretest for immediate group), 8 weeks (posttest for immediate group, pretest for waitlist group), 16 weeks (posttest for waitlist group)
|
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.
|
baseline (or pretest for immediate group), 8 weeks (posttest for immediate group, pretest for waitlist group), 16 weeks (posttest for waitlist group)
|
|
Change in Mobility Scale Score
Time Frame: baseline (or pretest for immediate group), 8 weeks (posttest for immediate group, pretest for waitlist group), 16 weeks (posttest for waitlist group)
|
Participant is asked to rate their level of confidence (1 extreme confidence to - 10 no confidence at all) that they will not fall in each of 10 activities.
Mean confidence level is calculated, lower scores indicate increased confidence.
|
baseline (or pretest for immediate group), 8 weeks (posttest for immediate group, pretest for waitlist group), 16 weeks (posttest for waitlist group)
|
|
Change in the Canadian Occupational Performance Measures (COPM)
Time Frame: baseline (or pretest for immediate group), 8 weeks (posttest for immediate group, pretest for waitlist group), 16 weeks (posttest for waitlist group)
|
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.
|
baseline (or pretest for immediate group), 8 weeks (posttest for immediate group, pretest for waitlist group), 16 weeks (posttest for waitlist group)
|
|
Change in Physical Activity Scale Score
Time Frame: baseline (or pretest for immediate group), 8 weeks (posttest for immediate group, pretest for waitlist group), 16 weeks (posttest for waitlist group)
|
12 items scored on a 4 point likert scale for a total possible range of scores from 0-36 where higher scores indicate more physical activity.
|
baseline (or pretest for immediate group), 8 weeks (posttest for immediate group, pretest for waitlist group), 16 weeks (posttest for waitlist group)
|
|
Change in Perceived Stress Scale Score
Time Frame: baseline (or pretest for immediate group), 8 weeks (posttest for immediate group, pretest for waitlist group), 16 weeks (posttest for waitlist group)
|
10 items scored on a 5 point likert scale for a total possible range of scores from 0-40 where higher scores indicate increased perceived stress.
|
baseline (or pretest for immediate group), 8 weeks (posttest for immediate group, pretest for waitlist group), 16 weeks (posttest for waitlist group)
|
|
Loneliness and Social Isolation Scale Score
Time Frame: baseline (or pretest for immediate group), 8 weeks (posttest for immediate group, pretest for waitlist group), 16 weeks (posttest for waitlist group)
|
26 items scored on a 4 point likert scale for a total possible range of scores from 0-96 where higher scores indicate increased feelings of loneliness and social isolation.
|
baseline (or pretest for immediate group), 8 weeks (posttest for immediate group, pretest for waitlist group), 16 weeks (posttest for waitlist group)
|
|
Social Network Scale Score
Time Frame: baseline (or pretest for immediate group), 8 weeks (posttest for immediate group, pretest for waitlist group), 16 weeks (posttest for waitlist group)
|
6 items scored on a 6 point likert scale for a total possible range of scores from 0-30 where higher scores indicate larger social network.
|
baseline (or pretest for immediate group), 8 weeks (posttest for immediate group, pretest for waitlist group), 16 weeks (posttest for waitlist group)
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2021-1278
- A176000 (Other Identifier: UW Madison)
- Protocol Approved 10/20/2021 (OTHER: UW Madison)
- ICTR Pilot (OTHER_GRANT: UWF Wisconsin Partnership)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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
-
Northwestern UniversityPotocsnak Human Longevity LabRecruitingAging | Aging Well | Aging, Biological | Aging, HealthyUnited States
-
TruDiagnosticBlushield USANot yet recruitingAging | Aging Well
-
Florida Institute for Human and Machine CognitionNot yet recruitingAging | Healthy Aging | Aging WellUnited States
-
University of West AtticaNot yet recruiting
-
Radboud University Medical CenterTerminated
-
Zhangzhou University ChinaCompletedQuality of Life | Well Aging | Aging Well | Well-Being, PsychologicalChina
-
National Hellenic Research FoundationTheracell Advanced BiotechnologyCompletedAging | Oxidative Stress | Well AgingGreece
-
Laval UniversityUniversité Catholique de LouvainCompletedAging | Older Adults | Aging WellCanada
-
National Institute of Rehabilitation, MexicoNot yet recruiting
-
TOPMEDNatural Sciences and Engineering Research Council, Canada; SEC Fonds Immobilier... and other collaboratorsCompleted
Clinical Trials on Yoga Via Telehealth - Immediately
-
University of Wisconsin, MadisonBader PhilanthropiesTerminated
-
Ankara UniversityCompleted
-
Abramson Cancer Center at Penn MedicineActive, not recruitingBody Weight | Overweight and Obesity | Cancer of Breast | Cancer SurvivorsUnited States
-
Texas Woman's UniversityWichita State UniversityRecruitingDiastasis RectiUnited States
-
Tuscaloosa Research & Education Advancement CorporationUnited States Department of DefenseNot yet recruitingCognitive Dysfunction | Mild Cognitive Impairment
-
University of WyomingCompletedTrauma | Posttraumatic Stress Disorder | Autism | Posttraumatic Stress SymptomUnited States
-
University of Dublin, Trinity CollegeHealth Research Board, IrelandCompletedGastric Cancer | Oesophageal CancerIreland
-
Teachers College, Columbia UniversityUniversity of MichiganCompletedDepression | Anxiety | Distress, Emotional | Emotional DysfunctionUnited States
-
Teachers College, Columbia UniversityRecruitingDepression | Anxiety | Distress, Emotional | Rumination | Self-Criticism | WorryUnited States
-
Teachers College, Columbia UniversityActive, not recruitingDepression | Anxiety | Distress, Emotional | Rumination | Self-Criticism | WorryUnited States