Hypertension Clinical Trial
To test the effectiveness of a stepped-care intervention involving 2 stages: (1) Self-Telemonitoring (STM) of blood pressure (BP) which uses a telephone transmission system (2) Telephone-Based Nurse Case Management (NCM), provided by a commercially available service.
DESIGN NARRATIVE:
The Medication Adherence and Blood Pressure Control Trial (ABC Trial) is a randomized
controlled trial in a multicultural population of uncontrolled, hypertensive patients to
test the effectiveness of a stepped-care intervention involving 2 stages: (1)
Self-Telemonitoring (STM) of blood pressure (BP) which uses a telephone transmission system
by which an easy-to-use modem, contained in the BP monitor, sends the BP measurements to a
commercial service (Lifelink Monitoring) who then sends the measurements to the patient's
health care provider; and (2) Telephone-Based Nurse Case Management (NCM), provided by a
commercially available service (U-Med). The nurse case managers will call patients
once/month, and provide counseling regarding BP control, and adherence to medication
regimens. All patients in the intervention condition will begin with STM; after 3 months,
patients whose BP has come under control remain in the STM condition; patients whose BP
remain uncontrolled are then randomized, half to NCM + Self-Telemonitoring; the other half
to continue in STM only (the design allows us to evaluate the effects of each arm of the
intervention separately, and the combination; in addition, there will be a Usual Care
condition). The focus is on an intervention strategy which readily transfers to a variety of
usual health care situations. Both interventions are commercially available, and therefore
are accessible to a wide range of health care providers, including smaller community-based
clinics. An innovative aspect of the intervention is that the 2 commercial services will
work together; the nurse case managers will receive BP reports from Lifelink, which the
nurse will then use as a basis for counseling. The effectiveness of the interventions will
be tested in 12 community-based clinics, which serve an economically disadvantaged, largely
African American and Hispanic population, in New York City. The main outcome measures are
medication adherence, determined by electronic drug event monitoring (MEMS), and pharmacy
refill records, as well as BP control. Study duration is 1 year. The multilevel focus of the
interventions is on provider as well as patient behavior. Reviews will be conducted for each
patient at study discharge, recording data on clinic BP measurements during the previous 12
months, if any, doctor appointments, ER visits, medication changes, and evidence that the
physician has responded to the interventions. The long-term goals of the research are to
assess the medical and cost effectiveness of the interventions separately, and combined.
;
Allocation: Randomized, Primary Purpose: Treatment
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