Pain Management App Study For Family Caregivers

  • STATUS
    Recruiting
  • days left to enroll
    26
  • sponsor
    Alzheimer’s Association
Updated on 23 September 2022
Investigator
Kristy Nguyen
Primary Contact
University of Iowa (online study) Contact
analgesic
dementia
Online studies
Accepts healthy volunteers

Summary

We are testing a web-based app that supports family caregivers in managing pain for patients with dementia. Family Caregivers will be asked to browse a web app and complete some tasks on the app, and then complete an online survey and an interview. The entire process will take approximately 1-2 hours. A $30 check will be provided for your participation.

Description

We would like to invite an adult family caregiver, who speaks and reads in English, and has managed pain and pain medication for a family member or a friend with dementia within the last 3 years. Family caregivers will be asked to do an one-time usability testing of our app. Family caregivers will browse a web app and complete some tasks on the app, and then complete an online survey and an interview. The entire process will take approximately 1-2 hours. A $30 check will be provided for participation.

Details
Condition Alzheimer's Disease, Dementia, Healthy Volunteers
Clinical Study IdentifierTX305368
SponsorAlzheimer’s Association
Last Modified on23 September 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

An adult family caregiver 1\. is older than 18 years old 2\. speaks and reads in English 3\. has managed moderate and severe pain (4 or greater than 4 on a 10-point scale) and pain medication for a family member/a friend with dementia within the last 3 years 4\. is willing and able to evaluate our app via a 1-time zoom meeting and then complete an online survey and an interview

Exclusion Criteria

A caregiver who does not meet our inclusion criteria
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How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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