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A Mobile Intervention Merging Yoga and Self-Management Skills

A Mobile Intervention Merging Yoga and Self-Management Skills (MY-Skills Mobile) for Older Adults With Multiple Chronic Conditions and Their Care-Partners

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04758312
Acronym
MYSkillsMobile
Enrollment
30
Registered
2021-02-17
Start date
2021-03-01
Completion date
2022-06-01
Last updated
2022-12-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Disease

Brief summary

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.

Interventions

BEHAVIORALMY-Skills Mobile

Yoga and Self-Management Education

Sponsors

Colorado State University
CollaboratorOTHER
Clemson University
CollaboratorOTHER
University of Southern California
CollaboratorOTHER
University of Colorado, Denver
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

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.

Design outcomes

Primary

MeasureTime frameDescription
User Mobile Application Rating Scale8 WeeksUsability; 20 items; Range 0-25, Higher score indicates better usability

Secondary

MeasureTime frameDescription
Patient Health Questionaire-88 weeksDepressive Symptoms; 8 items; Range 0-24; Higher score indicates worse depression
PROMIS Physical Function8 weeksPhysical Function; 20 items with 4 additional global items; Range 0-120; Higher scores indicate better function
PROMIS Self-Efficacy for Managing Chronic Conditions8 weeksSelf-Efficacy; 24 items; Range 0-120; Higher scores indicate better self-efficacy
PROMIS Companionship, Emotional, Instrumental Support8 weeksSocial Support; 14 items, Range 0-70; Higher scores indicate better social support

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026