AURA: Connecting Audio and Radio Sensing Systems to Improve Care at Home
Study Details
Study Description
Brief Summary
This is a proof-of-concept pilot randomized clinical trial to test the usability and feasibility of the innovative Audio + Radio (AURA) system to enhance personalized supportive care for cancer patients and caregivers during post-ostomy care transition.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
In this proof-of-concept study, our multidisciplinary team will conduct a pilot randomized clinical trial to test the feasibility of the innovative AUdio + RAdio (AURA) system to enhance personalized supportive care for cancer patients and caregivers during post-treatment care transition. The investigators will randomly assign 30 cancer patients with newly created ostomies for cancer treatment with curative intent and their primary caregivers to the AURA or usual care groups (30 patient-caregiver dyads, a total of 60 individuals). AURA is defined as a system that connects audio-based voice assistant devices with radiofrequency (RF) sensing technology to gather relevant patient information automatically, interactively, and with context-awareness and to store a patient's health records that otherwise had to be measured and entered manually into an electronic system. The users of this system will be the entire care team, consisting of the patient and their family members as well as the caregivers and healthcare providers at remote sites. The investigators will conduct pre- and post-assessments of quality of life (QOL) and patient-reported outcomes (PRO, symptoms) at baseline upon enrollment and 2 months later. If results indicate that the pilot trial is feasible, the investigators will design and conduct a definitive trial to examine the efficacy of AURA, a potentially scalable intervention that can be disseminated through oncology clinics nationwide to enhance post-treatment care for cancer patients with ostomies who transition from hospital professional care to self-management at home and their caregivers.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: AURA In addition to usual care, participants assigned to this arm will have access to our Audio + Radio (AURA) system. |
Behavioral: Audio + Radio (AURA)
Participants will receive personalized self-care information and guidance based on their symptoms and signs of complications (e.g., skin infection, fatigue) from interacting with our voice assistant device, connected to a system that integrating the PRO (e.g., fatigue) and objective data from passive RF sensing to provide continuous monitoring of patients' symptoms and complications after they are discharged home. AURA will triage patient care based on the monitoring data that indicate the severity of their symptoms and complications. Patients and caregivers will self-monitor and manage at home for mild and moderate symptoms but be referred to professionals (e.g., wound and stoma nurse) when the patient experiences severe symptoms or significantly worsened symptoms.
|
| No Intervention: Usual Care Participants assigned to this arm will receive the standard of care that is provided to all patients. |
Outcome Measures
Primary Outcome Measures
- Recruitment Rate [from study launching to ending, about 1 year]
Recruitment rate will be assessed by the percentage of potentially eligible participants who have consented to participate in the study
- Enrollment rate [after T1 (baseline survey)]
Enrollment rate will be assessed by the percentage of potentially eligible participants who have completed the baseline survey.
- Retention rate [after T2 (1-month followup survey)]
Retention rate will be assessed by the percentage of enrolled participants who have completed the 30-day followup survey at the end of the study period.
- Satisfaction with the AURA system [after T2 (1-month followup survey)]
Satisfaction with the AURA system will be assessed by the 9-item Participant Satisfaction Scale measuring the level of program satisfaction ranging from 1=not satisfied to 5=extremely satisfied. Higher total score indicates greater program satisfaction.
- Perceived ease of use of the PRISMS program [after T2 (1-month followup survey)]
Perceived ease of use of the AURA system will be assessed by the 23-item Usability Scale measuring the ease of use in three aspects: general, content, and navigation. The scales range from 1=strongly disagree to 5=strongly agree. Higher total score indicates greater ease of use.
Secondary Outcome Measures
- Change of Quality of Life (QOL) [T1 (baseline survey) and T2 (1-month followup survey)]
Quality of Life (QoL) will be assessed using the Functional Assessment of Cancer Therapy General Scale (FACT-G) v.4, a 27-item measure yielding total score and scores for physical, social/family, emotional, and functional well-being of demonstrated reliability, validity, and sensitivity to change. FACT-G consists of 4 subscales: physical well-being (PWB), functional well-being (FWB), emotional well-being (EWB) and social well-being (SWB). Scores on the four subscales are summed to produce a total score ranging from 0 to 108 with higher scores indicating better quality of life. Change in the FACT-G scores from T1 (baseline survey) to T2 (2-month followup survey) will be calculated.
Eligibility Criteria
Criteria
Inclusion Criteria
Phase I: The investigators will only be recruiting patients for this phase
Patients must:
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have been surgically treated for colorectal or bladder cancer with curative intent;
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have had an ostomy with curative intent for at least 90 days;
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be able to read and speak English;
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be 18 years or older;
Phase II: The investigators will be recruiting patients and caregivers as a dyad for this phase
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Patients must:
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have been surgically treated for colorectal or bladder cancer with curative intent;
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be within one month of hospital discharge of a newly created ostomy with curative intent;
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be able to read and speak English;
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be 18 years or older;
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have a caregiver who is willing to participate in the study;
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Caregivers must:
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be 18 years or older;
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be able to read and speak English;
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be identified as the primary caregiver by the patient;
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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).
Exclusion Criteria
Patients and their caregivers will be excluded if they:
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are unable to read, speak, or understand English;
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have more than one type of ostomy;
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have other cancer diagnosis (excluding non-melanomatous skin cancer); or
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have cognitive impairment (assessed by the Short Portable Mental Status Questionnaire).
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University of North Carolina at Chapel Hill | Chapel Hill | North Carolina | United States | 27599 |
Sponsors and Collaborators
- UNC Lineberger Comprehensive Cancer Center
Investigators
- Principal Investigator: Lixin Song, PhD, University of North Carolina, Chapel Hill
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- LCCC2123