E-Tailored Pain Management Support for Dementia Family Caregivers

Status: Recruiting
Location: See location...
Intervention Type: Other, Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 100
Healthy Volunteers: t
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• 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.

Locations
United States
Iowa
College of Nursing
RECRUITING
Iowa City
Contact Information
Primary
Nai-Ching Chi, PhD, MS, BSN
nai-ching-chi@uiowa.edu
319-335-7064
Backup
Gabriel M Vald, MS, BA
gmvald@uiowa.edu
515-897-8517
Time Frame
Start Date: 2025-05-22
Estimated Completion Date: 2026-05
Participants
Target number of participants: 60
Treatments
Active_comparator: Usual Care Group
Care recipients will continue receiving their regular pain care. Caregivers will complete outcome assessments only.~Introductory Meeting (Baseline):~Caregivers will attend a 1.5-hour meeting to complete informed consent and baseline REDCap surveys.~Follow-up (Month 1 and Month 2):~At 1-month and 2-month follow-ups, caregivers will independently complete REDCap surveys (\~45 minutes per follow-up).
Experimental: App Use Group
Care recipients will continue receiving their regular pain care. Caregivers will use the PACE-app and complete outcome assessments.~Introductory Meeting (Baseline):~Caregivers will attend a 1.5-hour meeting to complete informed consent and baseline REDCap surveys.~Intervention Period (Month 1):~Caregivers will use the PACE-app for 1 month, complete a daily pain diary (5-10 minutes/day), and access weekly summary reports to share with providers.~Post-Intervention (Month 1):~Caregivers will complete REDCap surveys and participate in a 1.5-hour interview on their experience with the app (audio-recorded unless declined).~Follow-up (Month 2):~Caregivers will complete the same REDCap questionnaires to assess longer-term outcomes.
Related Therapeutic Areas
Sponsors
Collaborators: Alzheimer's Association
Leads: University of Iowa

This content was sourced from clinicaltrials.gov