NCT05344950Completed
Connecting Audio and Radio Sensing Systems to Improve Care at Home
Development and Pilot Testing of AURA
Source: ClinicalTrials.gov · Last updated 19 Sept 2024
Brief summary (registry, in English)
This study aims to assess the usability of the innovative Audio + Radio (AURA) system in enhancing personalized supportive care for cancer patients and caregivers during the post-ostomy care transition by collecting information on patient's daily activities and answers to survey questionnaire, and enabling access to this information through a voice assistant device.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 13 (actual)
- First submitted
- 19 Apr 2022
- Start date
- 21 Mar 2022
- Primary completion date
- 31 Jul 2024
- Lead sponsor
- UNC Lineberger Comprehensive Cancer Center
- NCT number
- NCT05344950
What you commit to
- Study type: Observational
- Participants enrolled: 13
- From 21 Mar 2022 to the primary completion date, 31 Jul 2024
- 2 sites 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 illness
- have other cancer diagnosis (excluding non-melanomatous skin cancer); or
- have cognitive impairment (assessed by the Short Portable Mental Status Questionnaire).
Other
- Patients and their caregivers will be excluded if they:
- are unable to read, speak, or understand English;
- have more than one type of ostomy;
Who the study is looking for
- Phase I: The investigators will only be recruiting patients for this phase
- Patients must:
- have been surgically treated for colorectal or bladder cancer with curative intent;
- have had an ostomy with curative intent for at least 90 days;
- be able to read and speak English;
- be 18 years or older;
- Phase II: The investigators will be recruiting patients and caregivers as a dyad for this phase
- Patients must:
- have been surgically treated for colorectal or bladder cancer with curative intent;
- be within one month of hospital discharge of a newly created ostomy with curative intent;
- be able to read and speak English;
- be 18 years or older;
- have a caregiver who is willing to participate in the study;
- Caregivers must:
- be 18 years or older;
- be able to read and speak English;
- be identified as the primary caregiver by the patient;
- have not themselves been diagnosed with cancer or received cancer treatment during the study (to ensure that patients and caregivers focus their efforts on care of the patient).
Age in the registry: 18 years to 99 years · Sex: All · Does not accept healthy volunteers
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of North Carolina at Chapel Hill Coordinator of this site? Confirm its status | Chapel Hill | United States | Unknown status |
| UT Health San Antonio - MD Anderson Cancer Center Coordinator of this site? Confirm its status | San Antonio | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.