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Faith-based Approaches in the Treatment of Hypertension (FAITH)

Faith-based Approaches in the Treatment of Hypertension (FAITH)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01065831
Acronym
FAITH
Enrollment
373
Registered
2010-02-09
Start date
2010-11-30
Completion date
2014-06-30
Last updated
2016-03-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Keywords

motivational interviewing, lay health advisers

Brief summary

The purpose of this study is to test the effect of a church-based lifestyle intervention on blood pressure reduction in 400 hypertensive blacks (BP\> 140/90 mm hg).

Detailed description

This study will test the effectiveness of a church-based lifestyle intervention in improving blood pressure control among 400 hypertensive blacks in a group randomized controlled trial. The lifestyle intervention will be delivered by trained lay health advisers through group-based behavioral counseling and motivational interviewing (MINT-TLC) in 24 predominantly black churches in New York City.

Interventions

BEHAVIORALMotivational interviewing (MINT-TLC)

The MINT-TLC lifestyle intervention lead by lay health advisers will be compared to the health education attention control condition (CC). Twenty churches will participate in the study and each church will be randomly assigned to receive either MINT-TLC or CC. They will be compared on blood pressure reduction, physical activity levels, intake of fruits and vegetables, and weight reduction.

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH
NYU Langone Health
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 18 years or older * Diagnosis of hypertension * Self-identified Black or African American * SBP \> 140 mmHg or DBP \> 90 mmHg (based on the average of 3 blood pressure readings); or average SBP \> 130 mm Hg or DBP \> 80 mm hg (for those with diabetes or kidney disease) at the screening/baseline visits * Able to speak English

Exclusion criteria

* Unable to comply with the study protocol (either self-selected or by indicating during screening that s/he could not complete all requested tasks). * Pregnancy

Design outcomes

Primary

MeasureTime frame
Within-individual change in systolic blood pressure and diastolic blood pressure6 months

Secondary

MeasureTime frame
Levels of physical activity6 months
Percent change in weight6 months
Dietary intake of fruits and vegetables6 months
Proportion of blood pressure control9 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026