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Psychosocial Determinants of Medication Adherence in Hypertensive African Americans

Weill Cornell Medicine (WCM) logo

Weill Cornell Medicine (WCM)

Status

Unknown

Conditions

Hypertension

Treatments

Behavioral: Self affirmation and positive affect induction vs. control

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT00195182
0302006001

Details and patient eligibility

About

The specific aims for this study are:

  1. To examine the relationship between perceived racism and medication adherence among hypertensive African-American patients.
  2. To determine if psychological stress and depression mediate the relationship between perceived racism and medication adherence.

Full description

Achieving and maintaining recommended blood pressure goals in hypertensive African Americans is paramount to addressing racial disparities in hypertension-related morbidity and mortality. Because antihypertensive therapy is the cornerstone of hypertension management, good medication adherence is the key to adequate blood pressure control. Successful approaches to racial disparities must address how to increase adherence to anti-hypertensive medications.

Adherence to anti-hypertensive medications is likely multifactorial, and not solely related to SES or access to medical care. Psychosocial factors such as stress and depression have been implicated as important determinants of medication adherence. However, little is known about how other psychosocial factors such as perceived racism impact anti-hypertensive medication adherence. Understanding these relationships may assist in the development of targeted strategies to achieve good medication adherence in hypertensive patients.

The objective is to understand the relationships between perceived racism and medication adherence, while examining the role of depression, psychological stress, and self-efficacy in a population of hypertensive African-American patients. 262 African American adult hypertensive patients will be recruited from an urban academic general medicine practice. Baseline data collection will include assessments of demographics and socioeconomic status, clinical history and hypertension characteristics, depressive symptoms, perceived stress, and medication adherence. Patients will be followed for 1 year, when final evaluations will take place, including assessment of hypertension, stress, depression, medication adherence and level of perceived racism (measured by a validated instrument). The primary outcome is the change in medication adherence scores from baseline to 12 months. Statistical models will be developed to determine if level of perceived racism is associated with medication adherence, and whether stress and depression play a role in this relationship.

Enrollment

262 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients must be self-identified as African American.
  2. All patients must be aged 18 years or older.
  3. All patients must be diagnosed as having hypertension (for this project, hypertension will be defined according to the widely accepted criteria of the 6th Joint National Committee Guidelines on Prevention, Detection, Evaluation and Treatment of Hypertension, specifically a systolic blood pressure >140 mm hg or a diastolic blood pressure >90 mm hg) or if patients are taking any prescribed anti-hypertensive medication.
  4. Patients must be able to provide informed consent in English.

Exclusion criteria

  1. Patients who are unable to walk several blocks for any reason.
  2. Patients who refused to participate.
  3. Patients who are unable to provide informed consent.

Trial design

262 participants in 2 patient groups

1. No intervention
Description:
This group received follow-up every 2-months for one year. Follow-up included questions about their blood pressure and how well they had been able to adhere to their medication goal.
Treatment:
Behavioral: Self affirmation and positive affect induction vs. control
2. Experimental
Description:
This group received follow-up every 2-months for one year. Follow-up included questions about their blood pressure and how well they had been able to engage adhere to their medication goal. The intervention included receiving an additional educational workbook about using positive affect and self affirmation, as well as participating in using positive affect and self-affirmation to motivate behavior change, which in this case was to increase their physical activity level.
Treatment:
Behavioral: Self affirmation and positive affect induction vs. control

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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