Preventing Cognitive Decline by Reducing BP Target Trial

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The PCOT study is a multi-site randomized trial of patients 70 years or older with high BP. The main goal of the study Preventing Cognitive Decline by Reducing BP Target Trial (PCOT) is to conduct a large pragmatic clinical trial (PCT) to test the hypothesis that patients who receive care with a combination of clinical decision support (CDS) and team-based care delivered in primary care practices will have better blood pressure control and a lower incidence of mild cognitive impairment and dementia than patients receiving usual medical care. Patients will be recruited from UT Southwestern Medical Center and Parkland Health \& Hospital System.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 70
Healthy Volunteers: f
View:

• High BP defined as at least 1 BP readings of SBP \>= 130 or DBP \>=80 during the 24 months prior to enrollment

• Clinic visit with primary care provider within the last 24 months

• Ability to write and speak English or Spanish

• 70 years of age or older

• Ability to understand and willingness to provide informed consent

• Owns a smartphone

Locations
United States
Texas
UT Southwestern Medical Center
RECRUITING
Dallas
Contact Information
Primary
Venkatraghavan Sundaram, Ph.D.
venkatraghavan.sundaram@phhs.org
214-590-3848
Backup
Miguel Vazquez, MD
miguel.vazquez@utsoutwestern.edu
214-648-3442
Time Frame
Start Date: 2022-07-11
Estimated Completion Date: 2025-08-31
Participants
Target number of participants: 4000
Treatments
Experimental: Intervention Arm
Home BP data will be averaged each month via OmronConnect app on the patients' smartphone, which is programmed to send home BP readings to MyChart via Apple or Google Health.Participants whose home blood pressure reading average is systolic ≥ 130 and diastolic ≥ 80 will trigger the CDS (Clinical Decision Support) tool to assist their physicians with their blood pressure management. Study Team will not be involved in treatment decision making, it will be determined by subject's treating physician. .
No_intervention: Usual Care Arm
Physicians will continue to make decisions about the participant's blood hypertension management as usual without the CDS tool.
Related Therapeutic Areas
Sponsors
Collaborators: Parkland Health and Hospital System, National Institute on Aging (NIA), Duke University
Leads: University of Texas Southwestern Medical Center

This content was sourced from clinicaltrials.gov