Video-based Intervention to Address Disparities in Blood Pressure Control After Stroke (NCT05264298) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Video-based Intervention to Address Disparities in Blood Pressure Control After Stroke
United States542 participantsStarted 2022-03-29
Plain-language summary
The purpose of this study is to examine the impact of a multidisciplinary telehealth-based model of outpatient stroke care on blood pressure control following stroke, and further, to evaluate its impact on racial disparities in post-stroke blood pressure control.
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
* Ischemic stroke, hemorrhagic stroke (intracerebral hemorrhage),or transient ischemic attack (TIA
* Presence of hypertension (by clinical history or hospital BP ≥140/90 mmHg on two occasions)
* Plan to discharge home after stroke
* Ability to provide consent (patient or caregiver) in English or Spanish. Patients with cognitive impairment or aphasia limiting participation will be included if they have a caregiver to assist with monitoring and telehealth visits.
* Two neurologists must agree on TIA diagnosis
Exclusion Criteria:
* Modified Rankin scale (mRs) \> 4 (severe disability) at time of discharge
* Life expectancy \< 1 year or terminal illness
* Stroke unrelated to vascular risk factors (RFs) (drug use, trauma, vasculitis)
* Pregnancy
* Symptomatic flow limiting carotid stenosis without plan for intervention
* Long-term BP goal ≥ 130/80 mmHg according to clinical team
What they're measuring
1
6 month blood pressure control (24-hour ambulatory)
Timeframe: 6 months after discharge
Trial details
NCT IDNCT05264298
SponsorThe University of Texas Health Science Center, Houston