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Program for Research on the Outcomes of VA Education (PROVE)

V

VA New York Harbor Healthcare System

Status

Completed

Conditions

Hypertension
Smoking Cessation

Treatments

Other: Education
Other: Panel Management Support
Other: Data

Study type

Interventional

Funder types

Other U.S. Federal agency

Identifiers

NCT01677533
EDU 08-428-2

Details and patient eligibility

About

The PROVE aims to test the efficacy of panel management support and educational intervention in VA Primary Care Clinical Microsystems. The study will test three increasingly intensive methods for implementing panel management strategies among health care providers in VA primary care clinics: providing only panel data, providing panel management support, and providing support plus clinical microsystem-enhancing education and training.It is hypothesized that the group receiving panel management and educational interventions will have better smoking cessation and hypertension outcomes than the group receiving only panel management assistance. It is further supposed that the later will have better smoking cessation and hypertension patient outcomes than the data-only group.

Full description

Objective:

The specific aims for this study are: (1) to identify health professional educational and clinical microsystem determinants of outcomes for hypertension and smoking cessation in veterans. (2) to test the efficacy of three increasingly intensive methods for implementing panel management strategies among health care providers in VA primary care clinics: providing only panel data, providing panel management support, and providing support plus clinical microsystem-enhancing education and training.

Research design:

This project will consist of two phases. Phase I (one year) is the development of the necessary measurement and data infrastructure to assess health professional education, microsystem function, and clinical outcomes. In Phase 2 (two years) the study team will conduct a clinical demonstration project, comparing three interventions in a randomized controlled trial. Primary care teams will be randomly allocated to one of three arms: 1) panel management data, 2) panel management data and support, and 3) panel management data, support and education. The investigators will assess the impact of the implementation of panel management on primary patient outcomes in hypertension and smoking cessation (blood pressure and quit rates). The investigative team will also assess the impact of the implementation of panel management on secondary, intermediary, patient (patient activation, adherence, behavior change), provider (knowledge and attitudes, self-efficacy, job satisfaction) and microsystem outcomes (collective efficacy, teamwork, use of data, redesign of patient processes and provider roles/responsibilities, use of panel management strategies).

Methodology:

The study will utilize a multi-method, quasi-experimental design at VA NYHHS. Primary care is delivered through two teams at the Manhattan and five teams at the Brooklyn campuses. Patients, staff, nurses, and physicians are assigned to specific teams, thereby limiting contamination in this study.

Enrollment

5,000 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • non-specialized primary care clinical microsystems

Exclusion criteria

  • specialized clinical microsystems
  • pilot clinical patient-aligned care teams

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

5,000 participants in 3 patient groups

PM-Data
Active Comparator group
Description:
Team will receive data only.
Treatment:
Other: Data
PM-Support
Experimental group
Description:
Team will receive data and panel management support
Treatment:
Other: Data
Other: Panel Management Support
PM-Education
Experimental group
Description:
Team will receive data, panel management support, and educational interventions.
Treatment:
Other: Data
Other: Panel Management Support
Other: Education

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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