CompletedNot Applicable

COmmuNity-engaged SimULation Training for Blood Pressure Control

United States118 participantsStarted 2018-08-13

Plain-language summary

The goal of CONSULT-BP is to train early-stage healthcare providers, including residents and nurse practitioner (NP) students, to mitigate providers' bias, improve communication skills, and enhance providers' ability to develop authentic and meaningful therapeutic alliances with patients. The study setting is an academic safety net hospital that serves a large non-White and poor population. The Investigators hypothesize that patients' outcomes (blood pressure levels) will be lower after the training intervention compared with before training (control) periods.

Who can participate

SexALL

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Inclusion criteria

✓. Practice at a clinical site supported by an EMR to allow clinical data collection for outcome measurement
✓. 15-week clinical look-back period
✓. No prior completion of the CONSULT-BP intervention

Exclusion criteria

✕. English-speaking
✕. Non-White racial/ethnic minority or Medicaid recipient (regardless of race/ethnicity)
✕. Hypertension identified in the EMR
✕. Enrolled in hospice.
✕. Pregnancy, dementia, schizophrenia, bipolar illness, or other serious medical co-morbidity that would interfere with hypertension self-control

What they're measuring

Blood Pressure

Timeframe: Control period is 6 months before the intervention and intervention period is up to 6 months after the intervention

Trial details

NCT IDNCT03375918

SponsorUniversity of Massachusetts, Worcester

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-12-31

Results submitted2024-01-18

View on ClinicalTrials.gov More Hypertension trials