E-Tailored Pain Management Support for Dementia Family Caregivers: Feasibility of the PACE-app
Recruiting now · Not applicable
Conditions studied: Care Giving Burden, Dementia, Chronic Pain, Pain Management, Palliative Care
In brief
The goal of this clinical trial is to test whether a web-based application called the Pain Control Enhancement App (PACE-app) can support family caregivers in managing pain for their care recipients with dementia. The main questions it aims to answer are: Is it feasible and acceptable for family caregivers to use the PACE-app? Does using the PACE-app improve caregiver self-efficacy in pain management, adherence to pain treatments, communication with care providers, well-being, and their care recipient's pain conditions? Researchers will compare caregivers who use the PACE-app to those who continue with their usual care practices to see if the app leads to better outcomes for both caregivers and care recipients. Participants will: Be randomly assigned to either the PACE-app group or a usual-care control group Complete online surveys at baseline, 1 month, and 2 months If assigned to the PACE-app group: Use the PACE-app for 1 month to receive tailored pain management strategies and tools, and record their care recipient's pain in a digital diary Participate in an interview about their experience with the app All participation activities can be done remotely or in person.
Key facts
- Study ID
- NCT07032350
- Run by
- University of Iowa
- People needed
- 60
- Starts
- 2025-05-22
- Expected to finish
- 2026-05-01
- Last updated by the study team
- 2025-06-29
Who can join
Age: 18 and older, up to 100. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Be a primary caregiver - (a family member, relative, or friend) of a person with dementia (or cognitive impairment) and chronic pain (lasting >3 months)'
- Be responsible for managing the care recipient's pain and pain treatments (including interpreting verbal or non-verbal pain communication).
- Be age 18 - 100.
- Be able to read and speak English.
- Have regular access to an electronic device (tablet, laptop, or computer) with internet connectivity (for using the app and participating in data collection).
- Be accessible by phone or email to schedule meetings.
- Be willing to commit to the full study duration and protocol.
You may not qualify if…
- Currently participating in another research study that could interfere with this intervention.
Where it is running
- College of Nursing — Iowa City, Iowa, United States (enrolling)
Full record on ClinicalTrials.gov
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