- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05552638
Telecare in Rural Senior Centers
September 5, 2023 updated by: Elizabeth K Rhodus
Feasibility to Embed Telecare in Rural Community Senior Centers
The objective of this project is to assess the feasibility of telehealth stations at community centers as a mechanism to increase healthcare access for older adults living in rural communities.
Study Overview
Study Type
Interventional
Enrollment (Estimated)
120
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Elizabeth K. Rhodus, PhD
- Phone Number: 859-257-5562
- Email: elizabeth.rhodus@uky.edu
Study Contact Backup
- Name: Jordan Harp, PhD
- Phone Number: 8595623178
- Email: jordan.harp@uky.edu
Study Locations
-
-
Kentucky
-
Lexington, Kentucky, United States, 40536
- Recruiting
- University of Kentucky
-
Contact:
- Elizabeth Rhodus
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
19 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Age of 21 years or older
- Independently capable to complete electronic survey form
- Cognitive capable to verbalize consent for semi-structured interview
Exclusion Criteria
- Unable to complete an electronic survey form
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Senior Center Members
Participants who are using the provided telehealth stations in senior centers.
|
The University of Kentucky (UK) will embed telehealth stations at community-based senior centers.
Individuals who utilize these telehealth stations will be invited to complete a demographic survey prior to their telehealth appointment.
Following their appointment, they will be invited to complete a semi-structured interview with the research team.
Participants who elect to use telehealth station will be doing so as telehealth visits already scheduled with patients as Standard of Care (SOC).
The telehealth station in the senior center will be used to increase ease and access to telehealth should the patient/provider choose to use such an approach (for example, in instances when the patient does not have sufficient technology, internet access, or capability to operate telehealth at home).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Feasibility of embedded telehealth stations in senior centers as mechanism to increase healthcare access for older adults.
Time Frame: 12 months
|
Feasibility will be measured based on acceptance of the telehealth program by community residents evident by 5 Telehealth healthcare contacts per month
|
12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 20, 2022
Primary Completion (Estimated)
May 1, 2024
Study Completion (Estimated)
May 1, 2024
Study Registration Dates
First Submitted
September 20, 2022
First Submitted That Met QC Criteria
September 20, 2022
First Posted (Actual)
September 23, 2022
Study Record Updates
Last Update Posted (Actual)
September 7, 2023
Last Update Submitted That Met QC Criteria
September 5, 2023
Last Verified
September 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 78017
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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