Clinical Trials Directory

Trials / Completed

CompletedNCT04581317

Connecting Seniors to Care

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
53 (actual)
Sponsor
The University of Texas Health Science Center, Houston · Academic / Other
Sex
All
Age
60 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to assess the feasibility of implementing the virtual assistant devices into the daily routine of participants and their caregivers,to measure social determinants of health,depression,cognitive impairment,nutritional and functional status in the cognitively impaired participants

Conditions

Interventions

TypeNameDescription
OTHERmealsParticipants will receive meals delivered to them by the Meals oN wheels(MOW) program for 6 weeks.
OTHERAES 8 basic usageFor the second 6 weeks, participants will continue to have meal deliveries and will now have the AES 8 device which can be used by the cognitively impaired participant and their caregiver. AES 8 devices will be installed in participant's homes by the study team and participants will be given basic instructions on using the device as well as a one-page handout that will include instructions on how to use and maintain privacy with their device. The study staff will continue to call twice a week to ask the 5 questions. At the end of the 6 weeks, a study team member will make an in-person visit to the participants' homes to measure FFP, MHS, CES-D, MOCA, ADL/IADLs, NSI, ZCBI, and TAM.
OTHERAES 8 advanced usageIn the third 6 weeks, the participants will continue to have meal deliveries and the AES 8 will be upgraded to provide an active intervention by asking the twice a week 5 questions through the device. The questions should be answered by the cognitively impaired older adult using the device, though the caregiver can still use the device for other basic services. The participant will be able to answer the questions verbally or by touch screen options displayed on the device.At the end of the 6 weeks, a study team member will make an in-person visit to the participants' homes to measure FFP, MHS, CES-D, MOCA, ADL/IADLs, NSI, ZCBI, and TAM.

Timeline

Start date
2021-01-19
Primary completion
2022-09-29
Completion
2022-12-31
First posted
2020-10-09
Last updated
2023-01-11

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04581317. Inclusion in this directory is not an endorsement.