Activate For Life: mHealth Intervention To Address Pain And Fatigue In Low-income Older Adults Aging In Place
CompletedNot applicableNCT03853148
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
The Overall Aim of the present proposal is to evaluate the feasibility of an integrated mind-body intervention, Activate for Life, to improve overall physical activity and mental health and reduce pain and fatigue, resulting in increased likelihood of Aging in Place. Both subjective self-report (i.e., Patient-Reported Outcomes Measurement Information System PROMIS measures of pain, fatigue, depression and anxiety) and objective accelerometer data will be collected, along with standardized measures of balance, strength, and stability. In addition, the measures will be complemented with biomarker-based measures of stress, including cortisol based and 1,5-AG anhydroglucitol assays before, during, and after treatment that are correlated with stress, and fatigue symptoms.
Study details
- Official title
- Activate For Life: A Nurse Delivered Hybrid Telehealth/mHealth Aging In Place Intervention To Address Pain And Fatigue In Low-income Older Adults
- Conditions
- Interventions
- Behavioral: Otago
- Behavioral: Gentle yogic breathing
- Behavioral: Behavioral Activation
- Behavioral: Caregiver Gentle yogic breathing
- Sponsor
- Medical University of South Carolina
- Collaborators
- National Institutes of Health (NIH); National Institute of Nursing Research (NINR)
- Start date
- 2019-02-06
- Primary completion
- 2022-04-30
- Sex
- All
- Age range
- from 45 Years
- Healthy volunteers
- true
- Results posted
- Yes, on ClinicalTrials.gov
- Countries
- United States
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion and Exclusion Criteria for Older Adults (Arms 1, 2, 3): * Males and females older adults 60 years of age and older living in a Humanities Foundation apartment complex or in their own homes * PROMIS pain interference score of eight or above and/or a PROMIS pain behavior score of 15 or above (for older adults) * Able to ambulate 150 feet with or without the use of an assistive device * Able to follow simple instructions * Able to read, speak, and write English, * Able to operate tablet device and wearable activity tracker, * Not currently enrolled in an exercise program. Exclusion Criteria: * Inability or unwillingness of participant to give informed consent, * Physical, cognitive, sensory or psychiatric disability that would limit participants from engaging in self-management program as noted by a Mini-Cog score of 0-2. * Unwillingness to wear a physical activity tracker during the course of the study. Inclusion and Exclusion Criteria for Caregivers (Arm 4) * CG must be able to speak and read English * CG must be 45 years of age or older * CG must be able to provide consent for himself or herself * CG must live with or on same property as the PWD * CG be primarily responsible for care provision of the PWD in the home (i.e., is not paid for services; provides 4 hours or more of care/day; assists with activities of daily living-ADLs) Exclusion Criteria: * CG for whom yoga techniques would be detrimental due to physical limitations, * CG who are enrolled in other Yoga-related clinical trials, or who are currently engaged in regular Yoga activity once per week or more.
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT03853148