Cut Your Pressure Too: The Los Angeles Barbershop Blood Pressure Study

Sponsor
Cedars-Sinai Medical Center (Other)
Overall Status
Completed
CT.gov ID
NCT02321618
Collaborator
National Institutes of Health (NIH) (NIH), National Heart, Lung, and Blood Institute (NHLBI) (NIH), The California Endowment (Other), University of California, Los Angeles (Other), Lincy Foundation (Other)
320
1
2
34.7
9.2

Study Details

Study Description

Brief Summary

African-American men suffer more than most other groups from hypertension (HTN) but often have less access and less contact with doctors. Previous work by the study's Principal Investigator in Dallas, Texas, and Altadena, California, showed that barbershops are an excellent place to identify black men with high blood pressure and to enlist the aid of their barbers as healthcare extenders.

The purpose of this study in Metro Los Angeles (LA) is to compare two types of barber-based patient-centered blood pressure programs to see which type is more effective in improving the customers' high blood pressure. One type emphasizes blood pressure medication and the other type emphasizes lifestyle modification for high blood pressure.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: BP measurement & pharmacy
  • Behavioral: BP educational materials
N/A

Detailed Description

Uncontrolled hypertension (HTN) is one of the most important causes of premature disability and death among non-Hispanic black men. Indeed, black men have the highest HTN death rate of any U.S. race, ethnic, or gender group, contributing to a lower life expectancy. The age-adjusted HTN-related death rate is 3.3-times higher among black men than white men. To address this major health disparity, the investigators designed a novel community-partnered team approach to improve HTN management among black men and prevent needless strokes, heart attacks, kidney failure, and heart failure.

HTN requires physician (or middle-level provider) interaction to optimize blood pressure (BP) medication; black men have less interaction than black women; and thus far lower rates of HTN treatment (73% vs. 86%) and control (36% vs. 50%). Black-owned barbershops are a uniquely personal setting to discuss health with influential male peers. Barbershop health outreach is well-established, but untested as a vehicle for improving HTN control. Scientific evaluation is crucial to best allocate finite healthcare dollars and avoid promoting a "community health industry" that benefits only the promoters.

Under-treatment of HTN is common in primary care due to competing demands on physicians' time. The best way to improve HTN control is with team-based approaches enlisting pharmacists. They are more accessible than physicians, more knowledgeable about medication, and receive training on patient education. The investigators' new conceptual model links the barber-based intervention to team-based care delivery.

The purpose of this research study is to compare this new conceptual model to another barber-based patient-centered blood pressure program to see which is more effective in improving high blood pressure among Black patrons of African American owned barbershops in LA. Patrons randomized to Group 1 (the new conceptual model) will provide blood pressure readings for patrons aged 35 to 79 years of age and refer those with HTN to a Clinical Pharmacist to work with their doctors in optimizing blood pressure medication.

Patrons of Group 1 shops will also be exposed to role model posters are not intended as recruitment materials, but rather are educational tools that intend to highlight positive experiences of participation. The text of the role model stories will in no way provide statements of the effectiveness of the intervention being evaluated by the present research study. Rather, they are the main health messaging tools needed to promote completion of the program in order to achieve the experiences described. Essentially the document will be used as an intervention tool for peer-based health messaging - stories from real customers in the barbershop modeling target behaviors leading that promote continued participation in the protocol by peers with the hopes of achieving to the detection, treatment, and control of high blood pressure. Each role model story will encourage one of two desired health behaviors of potential subjects with elevated BP: 1) ask the barber to check patients' BP with each haircut, 2) schedule a follow-up visit with the study pharmacist to get patient's blood pressure under control. Large posters in the barbershop will show the model customer, his barber, and the study pharmacist who facilitated the desired behavior change. The model's (participants) own words will be used on the poster.

Group 2 barbershop patrons will be exposed to up-to-date information on high blood pressure and on lifestyle topics for blood pressure and heart health including weight management, healthy cooking, cholesterol lowering, and exercise.

A pre-specified cross-sectional sub study utilized the trial's initial screening population to test for an association between self-reported nocturia (>2 nightly/voids) and elevated daytime (in-barbershop) blood pressure.

Study Design

Study Type:
Interventional
Actual Enrollment :
320 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Barber-Pharmacist Coordination to Improve Blood Pressure Management in Black Men
Actual Study Start Date :
Feb 17, 2015
Actual Primary Completion Date :
Jun 30, 2017
Actual Study Completion Date :
Jan 9, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: BP measurement & pharmacy

BP measurements performed by barber, role model poster exposure in barbershop, and BP medication management visits with study pharmacist

Behavioral: BP measurement & pharmacy
Blood pressure monitoring by barber, blood pressure medication management by pharmacist, role model posters encouraging program participation

Other: BP educational materials

Exposure to hypertension educational materials in barbershop

Behavioral: BP educational materials
Exposure to hypertension educational materials

Outcome Measures

Primary Outcome Measures

  1. Primary Blood Pressure Outcome - change in systolic blood pressure [6 months]

    The pre-specified primary outcome was the change in systolic blood pressure from baseline to 6 months follow-up.

Secondary Outcome Measures

  1. Secondary Blood Pressure Outcome - change in diastolic blood pressure [6 months]

    The change in diastolic blood pressure from baseline to 6 month follow-up

  2. The percentage of participants achieving blood pressure goal [6 months]

    The percentage of participants who achieved blood pressure goal after 6 months follow-up (140/90,135/85, 130/80)

  3. The change in number/type of drug classes prescribed [6 months]

    The change in number/class of prescription drugs prescribed from baseline to 6 month follow-up

  4. Adverse Drug Reactions [6 months]

    The number and type of adverse drug reactions reported from baseline to 6 month follow-up

  5. Self-Rated Health [6 months]

    The change in self-rated health score from baseline to 6 month follow-up

  6. Self-Rated Patient Engagement [6 months]

    The change in PACIC patient engagement score from baseline to 6 month follow-up

Other Outcome Measures

  1. Extension Study Primary Blood Pressure Outcome - change in systolic blood pressure [12 months]

    The primary outcome of the extension study is the change in systolic blood pressure from baseline to 12 months follow-up.

  2. Extension Study Secondary Blood Pressure Outcome - change in diastolic blood pressure [12 months]

    The change in diastolic blood pressure from baseline to 12 month follow-up

  3. Extension Study Secondary Outcome - the percentage of participants achieving blood pressure goal [12 months]

    The percentage of participants who achieved blood pressure goal after 12 months follow-up (140/90,135/85, 130/80)

  4. Extension Study Secondary Outcome - the change in number/type of drug classes prescribed [12 months]

    The change in number/class of prescription drugs prescribed from baseline to 12 month follow-up

  5. Extension Study Secondary Outcome - adverse drug reactions [12 months]

    The number and type of adverse drug reactions reported from baseline to 12 month follow-up

  6. Extension Study Secondary Outcome - self-rated health [12 months]

    The change in self-rated health from baseline to 12 month follow-up

  7. Extension Study Secondary Outcome - self-rated patient engagement [12 months]

    The change in PACIC patient engagement score from baseline to 12 month follow-up

Eligibility Criteria

Criteria

Ages Eligible for Study:
35 Years to 79 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • 35 to 79 years of age

  • Non-Hispanic Black men

  • Long-term/frequent barbershop patronage (barbershop patrons having at least one haircut every 6 weeks in the same barbershop for the past 6 months).

  • Systolic BP >140 at 2 screenings on 2 separate days

  • Complete set of Baseline Data

Exclusion Criteria:
  • Women

  • Children

  • <35 years of age

  • Non-black

  • Hispanic ethnicity

  • New/infrequent patronage (<8 haircuts at same barbershop in last 12 months)

  • Systolic BP <140 at either screening

  • Currently receiving cancer chemotherapy

  • On Dialysis

  • Incomplete baseline data

  • Serious Plan to Move in the next 1.5 years

  • Plans to be out of the area for > 1 month in the next 1.5 years

Contacts and Locations

Locations

Site City State Country Postal Code
1 Cedars-Sinai Medical Center Los Angeles California United States 90048

Sponsors and Collaborators

  • Cedars-Sinai Medical Center
  • National Institutes of Health (NIH)
  • National Heart, Lung, and Blood Institute (NHLBI)
  • The California Endowment
  • University of California, Los Angeles
  • Lincy Foundation

Investigators

  • Principal Investigator: Ronald G Victor, MD, Cedars-Sinai Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ron Victor, DIRECTOR, CEDARS-SINAI HYPERTENSION CENTER DIRECTOR OF CLINICAL RESEARCH & ASSOCIATE DIRECTOR, HEART INSTITUTE BURNS AND ALLEN CHAIR IN CARDIOLOGY RESEARCH, Cedars-Sinai Medical Center
ClinicalTrials.gov Identifier:
NCT02321618
Other Study ID Numbers:
  • Pro00035347
  • 5R01HL117983-02
First Posted:
Dec 22, 2014
Last Update Posted:
Jul 10, 2018
Last Verified:
Jul 1, 2018
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Keywords provided by Ron Victor, DIRECTOR, CEDARS-SINAI HYPERTENSION CENTER DIRECTOR OF CLINICAL RESEARCH & ASSOCIATE DIRECTOR, HEART INSTITUTE BURNS AND ALLEN CHAIR IN CARDIOLOGY RESEARCH, Cedars-Sinai Medical Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 10, 2018