- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07428174
An Aging Healthy Intervention for Older Adults Delivered by Community Health Workers in Senior Centers: A Clinical Trial (aCT)
February 17, 2026 updated by: Martha Kubik, George Mason University
ageWELL in the Community Together (aCT) Study
The aCT Study will develop, implement and evaluate a community health worker (CHW) integrated model of care delivery for older adults that is senior center based.
CHW services will be available for older adult participants at three centers, 4 hours per week for 4 months.
Three centers will continue usual services.
Researchers will compare blood pressure, physical activity levels, fruit/vegetable consumption and psychosocial outcomes across groups before and after the intervention.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
The six senior centers are located in southeastern Kentucky.
The CHWs are community-based, certified in the state of Kentucky and employed by a local organization.
The CHW intervention will be guided by a training module developed by the researchers in collaboration with our collaborating partner, the University of Kentucky Center for Excellence in Rural Health that reflects evidence-based geriatric practices and formative assessment conducted in 2024/2025 with seniors and senior service administrators from the area
Study Type
Interventional
Enrollment (Estimated)
250
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: Martha Kubik, PhD
- Phone Number: 7039938870
- Email: mkubik@gmu.edu
Study Contact Backup
- Name: William Baker
- Phone Number: 8592183684
- Email: mace.baker@uky.edu
Study Locations
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-
Kentucky
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Hazard, Kentucky, United States, 41701
- University of Kentucky Center for Excellence in Rural Health
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-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria: Eligible participants will be age 60 years and older, registered as a meal program participant at a participating senior center and speak English.
Exclusion Criteria: Non-English speakers and older adults who access meal program services in senior centers not participating in the study are not eligible for study participation.
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: Prevention
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: aCT CHW Intervention
State-certified CHWs employed and supervised by Kentucky Homeplace, a local organization that provides training and CHW services to local communities, will deliver the intervention at three senior centers 4 hours per week for 4 months, which include health promotion and disease prevention services and programs, advocacy, and health screenings.
|
The aCT CHW intervention arm will be delivered by state-certified CHWs employed and supervised by Kentucky Homeplace, a local organization that provides training and CHW services to local communities.
Trained CHWs will deliver the intervention at three senior centers 4 hours per week for 4 months, which will include health promotion and disease prevention services and programs, advocacy, and health screenings.
|
|
No Intervention: Usual practice
Three other senior centers who have agreed to study participation will serve as comparison sites, where older adults who visit the centers will continue to access usual services which have not typically included on-site CHW services.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
blood pressure
Time Frame: Baseline following enrollment and 4-5 months later following completion of the intervention
|
Blood pressure will be measured in duplicate, with appropriate size cuff and participant seated, arm supported so elbow at heart level and following a 5 minute rest.
|
Baseline following enrollment and 4-5 months later following completion of the intervention
|
|
physical activity levels
Time Frame: Baseline following enrollment and 4-5 months later following intervention completion
|
We will use a self-report measure, the Rapid Assessment of Physical Activity (RAPA), a 9-item questionnaire validated for use in older adults
|
Baseline following enrollment and 4-5 months later following intervention completion
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Martha Kubik, PhD, George Mason University
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 (Estimated)
April 1, 2026
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
December 1, 2026
Study Registration Dates
First Submitted
February 17, 2026
First Submitted That Met QC Criteria
February 17, 2026
First Posted (Actual)
February 23, 2026
Study Record Updates
Last Update Posted (Actual)
February 23, 2026
Last Update Submitted That Met QC Criteria
February 17, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- STUDY00000967
- FP00006108 (Other Grant/Funding Number: National Foundation to End Senior Hunger)
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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