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Search / Trial NCT04797403

Implementation of Multifaceted Patient-Centered Treatment Strategies for Intensive Blood Pressure Control in Minimize Cognitive Decline

Launched by TULANE UNIVERSITY · Mar 11, 2021

Trial Information

Current as of May 28, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is looking at a new way to help people with high blood pressure (hypertension) to lower their blood pressure significantly, with the goal of preventing cognitive decline, which is the gradual loss of mental abilities. The study specifically focuses on racial minority and low-income patients in primary care settings. Researchers want to see if an intensive treatment plan that targets a blood pressure of less than 120 mmHg can help protect against issues related to thinking and memory, especially in groups that often face health disparities.

To be eligible for this study, participants should be at least 40 years old, with a focus on those over 60. They will need to have high blood pressure readings at previous doctor visits and cannot have a diagnosis of dementia or serious kidney disease. The study is open to both men and women who receive care at clinics that serve mostly underserved populations and have the necessary medical record systems in place. Participants will be involved in a treatment plan that aims to lower their blood pressure while being monitored by healthcare professionals. This research hopes to provide valuable insights that can be used to improve healthcare strategies for preventing cognitive decline in communities that need it most.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria for Primary Care Clinics
  • Predominantly managing underserved populations with health disparities (ethnic minorities, low-income groups, and residents of rural areas and inner cities).
  • Having electronic medical record systems.
  • Serving \>200 hypertension patients (ICD-10-CM I10-I15) during the previous year.
  • Not participating in other hypertension control programs
  • Not sharing providers or nurses/pharmacists with other participating clinics.
  • Inclusion Criteria for Study Participants
  • Men or women aged ≥40 years (2/3 of participants ≥60 years) who receive primary care from participating clinics.
  • Systolic BP ≥ 140 mmHg at two screening visits for those not taking antihypertensive medication or systolic BP ≥ 130 mmHg at two screening visits for those taking antihypertensive medications
  • Pregnant women, women planning to become pregnant in the near future, women of childbearing potential and not practicing birth control, and persons who cannot give informed consent will be excluded.
  • No diagnosis of dementia at baseline
  • Baseline MoCA score ≥ 10.
  • No diagnosis of end-stage renal disease, defined as dialysis or transplantation
  • Speak English as first language
  • No plans to change to a primary healthcare provider outside of their clinic in the near future
  • No individuals unlikely to complete the study, such as those who plan to move out of the study area in the near future and temporary migrant and homeless people
  • No immediate family members are staff at their clinic

About Tulane University

Tulane University, a prestigious institution located in New Orleans, Louisiana, is dedicated to advancing medical research and improving public health through innovative clinical trials. With a strong emphasis on interdisciplinary collaboration, Tulane leverages its extensive resources and expertise in various fields, including tropical medicine, infectious diseases, and population health. The university's commitment to ethical research practices and patient-centered approaches ensures that clinical trials conducted under its auspices not only contribute to scientific knowledge but also prioritize the well-being of participants. As a leader in clinical research, Tulane University aims to translate findings into tangible health solutions that benefit local communities and beyond.

Locations

New Orleans, Louisiana, United States

Patients applied

0 patients applied

Trial Officials

Katherine T Mills, PhD

Principal Investigator

Tulane University

Jiang He, MD, PhD

Principal Investigator

Tulane University

Jeff D Williamson, MD

Principal Investigator

Wake Forest University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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