- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04758312
A Mobile Intervention Merging Yoga and Self-Management Skills (MYSkillsMobile)
December 8, 2022 updated by: University of Colorado, Denver
A Mobile Intervention Merging Yoga and Self-Management Skills (MY-Skills Mobile) for Older Adults With Multiple Chronic Conditions and Their Care-Partners
Chronic disease self-management interventions and meditative movement approaches (.e.g., yoga) can independently improve depressive symptoms.
However, to our knowledge there are no interventions integrating evidence-based chronic disease management strategies with yoga to maximize physical, psychological or social outcomes, nor are mobile health platforms commonly used to improve the reach of these integrated interventions.
Therefore, we developed Merging-Yoga for Self-Management Skills Mobile (MY-Skills Mobile).
Our first aim is to adapt the MY-Skills Mobile to tailor the intervention to older adults with multiple chronic conditions (MCC) by convening a panel of patient and care-partner stakeholders.
We will convene four patient and care-partner dyads (N=8) to serve as study partners for three longitudinal focus groups to suggest and review MY-Skills Mobile adaptations.
We will then conduct a usability study of MY-Skills Mobile with older adults with MCC and their care-partners.
We will conduct two waves of rapid-cycle prototyping with 5 dyads in each wave (N=20).
Dyads will participate in MY-Skills Mobile modules.
We will then use acceptability surveys and use data in each wave to iteratively adapt MY-Skills Mobile to optimize usability and acceptability.
Study Overview
Study Type
Interventional
Enrollment (Actual)
30
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
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Colorado
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Aurora, Colorado, United States, 80045
- University of Colorado
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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
65 years and older (Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Older Adults with Multiple Chronic Conditions (MCC) and Depressive Symptoms:
- over the age of 65 at time of recruitment
- Multiple chronic conditions: Bayliss Disease Burden/Morbidity Assessment by Self-Report diagnosis > 2 and a disease burden score >2 indicating the presence of at least two chronic conditions that limit activities of daily of living.
- Presence of depressive symptoms will be screened by the Patient Health Questionnaire-2 Scale (PHQ-2), with a score of > 3 indicating at least mild depressive symptoms.
- Participants must be community dwelling
- Live in the United States
- Speak English
- Participants must be able to provide informed consent and have the ability to stand with or without an assistive device.
- We will also use the Patient Activity Readiness Questionnaire (PAR-Q) to determine the safety or possible risk of participation.
Care-Partners:
- Care-partners include any family, friend, or social support that the older adult identifies
- at least age 18
- Can provide informed consent
- Participants must be able to provide informed consent and have the ability to stand with or without an assistive device.
- We will also use the Patient Activity Readiness Questionnaire (PAR-Q) to determine the safety or possible risk of participation.
Exclusion Criteria for Older Adults with MCC and Care-Partners:
- Self-reported diagnosis of Alzheimer's disease or dementia
- Self-reported diagnosis of a severe mental health problem (e.g. schizophrenia, bipolar affective disorder or other psychotic illness)
- Consistent yoga >120 minutes a week
- Completed self-management education in the last year
Participants will not be excluded due to limited technology access. We will provide temporary tablets and mobile hotspot connectivity to interested participants that do not have hardware or internet access.
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: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: MY-Skills Mobile Intervention
MY-Skills Mobile is an 8-week intervention merging yoga and self-management offered via remote tools including Zoom (video-conferencing software), Canvas (education software), and Qualtrics (survey software) that can be accessed via a computer or tablet.
The self-management content is delivered primarily through asynchronous tools that include educational videos and interactive activities for goal setting, action plan, monitoring goals, and problem-solving practice.
Yoga is offered synchronously via Zoom two-times per week for 60 minutes (120 minutes per week).
The synchronous yoga sessions will be offered at a time that best accommodates participants' schedules.
Yoga will become progressively challenging over the eight weeks and will include seated and standing postures.
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Yoga and Self-Management Education
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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User Mobile Application Rating Scale
Time Frame: 8 Weeks
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Usability; 20 items; Range 0-25, Higher score indicates better usability
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8 Weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Patient Health Questionaire-8
Time Frame: 8 weeks
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Depressive Symptoms; 8 items; Range 0-24; Higher score indicates worse depression
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8 weeks
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PROMIS Physical Function
Time Frame: 8 weeks
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Physical Function; 20 items with 4 additional global items; Range 0-120; Higher scores indicate better function
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8 weeks
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PROMIS Self-Efficacy for Managing Chronic Conditions
Time Frame: 8 weeks
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Self-Efficacy; 24 items; Range 0-120; Higher scores indicate better self-efficacy
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8 weeks
|
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PROMIS Companionship, Emotional, Instrumental Support
Time Frame: 8 weeks
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Social Support; 14 items, Range 0-70; Higher scores indicate better social support
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8 weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Jennifer Portz, PhD, MSW, University of Colorado, Denver
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)
March 1, 2021
Primary Completion (Actual)
June 1, 2022
Study Completion (Actual)
June 1, 2022
Study Registration Dates
First Submitted
February 11, 2021
First Submitted That Met QC Criteria
February 12, 2021
First Posted (Actual)
February 17, 2021
Study Record Updates
Last Update Posted (Estimate)
December 12, 2022
Last Update Submitted That Met QC Criteria
December 8, 2022
Last Verified
December 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 21-2632
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
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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