Fact CheckerSign in

NCT07032350Recruiting

E-Tailored Pain Management Support for Dementia Family Caregivers: Feasibility of the PACE-app

E-Tailored Pain Management Support for Dementia Family Caregivers

Source: ClinicalTrials.gov · Last updated 29 Jun 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
19 Jun 2025
Start date
22 May 2025
Primary completion date
31 May 2026
Lead sponsor
University of Iowa
NCT number
NCT07032350

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From 22 May 2025 to the primary completion date, 31 May 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Currently participating in another research study that could interfere with this intervention.

Who the study is looking for

  • 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.

Age in the registry: 18 years to 100 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
College of Nursing
Coordinator of this site? Confirm its status
Iowa CityUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.