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CONSULT-BP Training for High Blood Pressure (CONSULT-BP Trial)

N/A
Waitlist Available
Led By Jennifer Tjia, MD, MSCE
Research Sponsored by University of Massachusetts, Worcester
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 3 months after the intervention
Awards & highlights

CONSULT-BP Trial Summary

This trial is testing whether a training intervention can help early-stage healthcare providers communicate better with patients and improve patients' blood pressure levels.

Who is the study for?
This trial is for early-stage healthcare providers who haven't done the CONSULT-BP training and work where they can track patient data. It's also for English-speaking patients who are non-White or on Medicaid with high blood pressure recorded in their medical records. First-year trainees, pregnant women, and patients with certain mental health conditions or serious illnesses that affect self-care are excluded.Check my eligibility
What is being tested?
The CONSULT-BP study tests an educational program aimed at improving healthcare providers' communication skills, reducing bias, and building better relationships with patients to help manage high blood pressure more effectively. The hypothesis is that this training will result in lower blood pressure levels in patients compared to before the providers received the training.See study design
What are the potential side effects?
Since this intervention involves education and skill development rather than medication or medical procedures, there aren't typical side effects like those associated with drugs or surgery. However, participants may experience stress or discomfort during role-playing exercises as part of the training.

CONSULT-BP Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 3 months after the intervention
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 3 months after the intervention for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Blood pressure
Secondary outcome measures
Blood Pressure Self Care Scale
Patient Reported Trust in Heathcare Provider
Quality of Communication
+1 more

CONSULT-BP Trial Design

5Treatment groups
Experimental Treatment
Group I: Healthcare Trainees - Cluster 5Experimental Treatment1 Intervention
Within each academic year, trainee clusters are randomized to 1 of 5 start date training times for Other: CONSULT-BP Educational Intervention. Each arm has a pre-intervention (control) period and a post-intervention (exposure) period.
Group II: Healthcare Trainees - Cluster 4Experimental Treatment1 Intervention
Within each academic year, trainee clusters are randomized to 1 of 5 start date training times for Other: CONSULT-BP Educational Intervention. Each arm has a pre-intervention (control) period and a post-intervention (exposure) period.
Group III: Healthcare Trainees - Cluster 3Experimental Treatment1 Intervention
Within each academic year, trainee clusters are randomized to 1 of 5 start date training times for Other: CONSULT-BP Educational Intervention. Each arm has a pre-intervention (control) period and a post-intervention (exposure) period.
Group IV: Healthcare Trainees - Cluster 2Experimental Treatment1 Intervention
Within each academic year, trainee clusters are randomized to 1 of 5 start date training times for Other: CONSULT-BP Educational Intervention. Each arm has a pre-intervention (control) period and a post-intervention (exposure) period.
Group V: Healthcare Trainees - Cluster 1Experimental Treatment1 Intervention
Within each academic year, trainee clusters are randomized to 1 of 5 start date training times for Other: CONSULT-BP Educational Intervention. Each arm has a pre-intervention (control) period and a post-intervention (exposure) period.

Find a Location

Who is running the clinical trial?

University of Massachusetts, WorcesterLead Sponsor
342 Previous Clinical Trials
976,405 Total Patients Enrolled
National Institute on Minority Health and Health Disparities (NIMHD)NIH
380 Previous Clinical Trials
1,215,449 Total Patients Enrolled
Jennifer Tjia, MD, MSCEPrincipal Investigator - UMass Medical School
University of Massachusetts, Worcester
2 Previous Clinical Trials
105 Total Patients Enrolled

Media Library

CONSULT-BP Educational Intervention Clinical Trial Eligibility Overview. Trial Name: NCT03375918 — N/A
High Blood Pressure Research Study Groups: Healthcare Trainees - Cluster 1, Healthcare Trainees - Cluster 2, Healthcare Trainees - Cluster 3, Healthcare Trainees - Cluster 4, Healthcare Trainees - Cluster 5
High Blood Pressure Clinical Trial 2023: CONSULT-BP Educational Intervention Highlights & Side Effects. Trial Name: NCT03375918 — N/A
CONSULT-BP Educational Intervention 2023 Treatment Timeline for Medical Study. Trial Name: NCT03375918 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

To what extent is this trial being administered to participants?

"Affirmative, according to clinicaltrials.gov this medical study is actively recruiting patients after first being posted on August 13th 2018 and last updated September 20th 2022. A total of 205 participants need to be enrolled across 5 sites for the trial's completion."

Answered by AI

Is this endeavor still open to enrollment?

"Confirmed. According to resources on clinicaltrials.gov, this medical experiment is still actively recruiting volunteers. It was first advertised back in August 2018 and the latest update came at the end of September 2022."

Answered by AI
~31 spots leftby Apr 2025