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Beta-Blockers in Heart Failure: Pharmacy-level Intervention Comparison

US Department of Veterans Affairs (VA) logo

US Department of Veterans Affairs (VA)

Status

Completed

Conditions

Heart Failure

Treatments

Other: Level 1: (provide site-specifi information)
Other: Level 2 (Provide site- and patient-specific information)

Study type

Interventional

Funder types

Other U.S. Federal agency

Identifiers

NCT01002456
VMS #120 (Other Identifier)
RRP 09-136

Details and patient eligibility

About

The overall objective of the proposed pilot study is to begin evaluation of two methods for promoting adherence to guidelines for beta-blocker therapy in heart failure. The design includes site level baseline measurement, feedback, remeasurement after six months, and randomized (by site) comparison samples. The setting is VA sites, with intervention directed at the pharmacy.

Full description

Current evidence-based guidelines in VA recommend one of three beta-blockers (carvedilol, metoprolol succinate, or bisoprolol) that have been shown to reduce mortality in heart failure patients with systolic dysfunction, with recommended target doses. However, Pharmacy Benefits Management (PBM) data indicate that prescribing for beta-blockers in heart failure patients that is not in accordance with guidelines is substantial, both in terms of the agent selected and the dose. Sites will be recruited and randomized to two different intensities of intervention to promote adherence to guidelines.

Enrollment

220 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • VA sites
  • Males and females

Exclusion criteria

none

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

220 participants in 2 patient groups

Level 1: site-specific information
Other group
Description:
provide site-specific information on nonadherence
Treatment:
Other: Level 1: (provide site-specifi information)
Level 2: site-, patient-specific info
Other group
Description:
provide site- and patient-specific information on nonadherence
Treatment:
Other: Level 2 (Provide site- and patient-specific information)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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