NCT07084051Completed
Improve Medication Adherence Among Stroke Survivors in Rural Kentucky
Intervention to Improve Medication Adherence Among Stroke Survivors in Rural Kentucky
Source: ClinicalTrials.gov · Last updated 26 Jan 2026
Brief summary (registry, in English)
To test the feasibility and promise of a combined intervention provided by community health worker (CHW) in collaboration with pharmacy technician and pharmacist to improve hypertension and long-term stroke outcomes by identifying and reducing barriers to medication adherence among ischemic stroke survivors. This collaborative intervention involves a self-management program including an educational session on practical strategies to improve hypertension control (i.e., appropriately taking medications, necessity of treatment, and consequences of not taking medicine, etc.), complemented by individually-tailored sessions to identify and address barriers to medication adherence.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 4 (actual)
- First submitted
- 16 Jul 2025
- Start date
- 24 Jul 2025
- Primary completion date
- 31 Dec 2025
- Lead sponsor
- Hend Mansoor
- Diseases
- Stroke
- NCT number
- NCT07084051
What you commit to
- Study type: Interventional
- Participants enrolled: 4
- From 24 Jul 2025 to the primary completion date, 31 Dec 2025
- 1 site 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.
Prior treatment
- a prior aneurysmal subarachnoid hemorrhage and or aneurysm, cerebral venous sinus thrombosis, vasculitis, blood clotting disorder due to genetic causes
- if the patient does not take any secondary preventative medications
Other illness
- cognitive impairment
- a terminal illness
Other
- significant aphasia
- other neurologic deficits that would impede from providing informed consent or meaningfully participate in the one-to-one sessions.
Who the study is looking for
- Adult patients with history of ischemic stroke or transient ischemic attack (TIA) in the past 2 years
- residing in a rural county in Kentucky
Age in the registry: 30 years to 90 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of Kentucky Coordinator of this site? Confirm its status | Lexington | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.