Skip to content

Counseling Older Adults to Control Hypertension

Counseling Older Adults to Control Hypertension

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01180673
Acronym
COACH
Enrollment
251
Registered
2010-08-12
Start date
2008-02-29
Completion date
2012-12-31
Last updated
2019-03-27

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

Conditions

Cardiovascular Diseases, Hypertension, Vascular Diseases

Keywords

Hypertension, Older Adults, Motivational Interviewing, Lifestyle Counseling, Senior Centers

Brief summary

This study will evaluate the effect of a senior center-based comprehensive therapeutic lifestyle intervention delivered through group-based counseling and motivational interviewing (MINT-TLC) among 250 hypertensive African American or Latino seniors age 60 and older in a randomized control trial.

Interventions

BEHAVIORALMINT-TLC

This intervention is based on established clinical practice guidelines for prevention and treatment of hypertension, which recommend weight loss (if overweight), limiting sodium and alcohol intake, regular physical activity, and eating a low-fat diet that is rich in fruit and vegetables. Seniors will attend weekly group classes conducted by trained research assistants for the first 12 weeks (intensive phase); followed by three individual motivational interview (MINT) sessions that will occur monthly over the next three months (extended phase); and finally each senior will receive three bi-monthly booster MINT sessions in the remaining six months (maintenance phase).

BEHAVIORALControl Condition

Seniors randomized to the control arm will receive a single individual brief advice session on therapeutic lifestyle changes recommended for blood pressure reduction. In addition, they will be given print versions of the NHLBI publications Your Guide to Lowering Blood Pressure; and Facts about the DASH Eating Plan. Sessions will be delivered by trained research assistants.

Sponsors

National Institute on Minority Health and Health Disparities (NIMHD)
CollaboratorNIH
Columbia University
CollaboratorOTHER
NYU Langone Health
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Age 60 years or older * Diagnosis of HTN * Taking at least one anti-hypertensive medication * Self-identified Black, African American, or Latino

Exclusion criteria

* Unable to comply with the study protocol * Participation in other hypertension studies * Severe hearing impairment * Severe visual impairment * Arm circumference \> 42 cm for large cuff, or arm circumference \> 52 cm for extra large cuff (if extra large cuff is available)

Design outcomes

Primary

MeasureTime frame
Within-individual change in systolic blood pressure and diastolic blood pressure from baseline to 12 months12 months

Secondary

MeasureTime frameDescription
Change in physical activity level from baseline to 12 months12 monthsPhysical activity is assessed using the Yale Physical Activity Scale (YPAS) and the International Physical Activity Questionnaire (IPAQ). Data collected with the YPAS will be reported as a final total activity dimension score. Data collected for the IPAQ will be expressed in MET-min per day or categorically (low, moderate, high).
Percent change in weight from baseline to 12 months12 months
Change in number of daily servings of fruits and vegetables from baseline to 12 months12 months
Proportion of participants with adequate blood pressure control at 12 months12 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026