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OpenTrials
Completed

NCT Number: NCT00115557

Delivery of Preventive Services in Primary Care

The major goal of this project is to determine the effectiveness of a multi-component intervention designed to help primary care practices implement three office system strategies known to increase delivery of immunizations and other preventive services. This two-year study will contribute to our understanding of multi-component translational interventions in primary care, and particularly within practice-based research networks.

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Key information

Age range

30 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

OKPRN

Oklahoma City, Oklahoma, 73104, United States

About this study

The multi-component translational intervention that we plan to test includes medical record audits with feedback and benchmarking, academic detailing by an opinion leader including information from literature review plus the advice of local exemplars, a practice facilitator, who will work with the practices over a six-month period, and an IT application that provides decision-support, prompts, and reminders to office staff and patients.

The proposed project will be a randomized controlled trial of a multi-component strategy designed to facilitate the incorporation into primary care practices of three office management components known to increase preventive service delivery rates: 1) nurse standing orders; 2) special immunization/ preventive services "clinics;" and 3) recall and reminder systems. Twenty-four practices, all members of a primary care practice-based research network, will be enrolled and randomized to receive the complete intervention or performance feedback with benchmarking only. The primary outcomes will be number of management components implemented. Characteristics of clinicians and practices that are associated with greater or lesser success in implementing the three strategies and barriers encountered will also be examined, and we will measure and compare rates of selected immunizations and preventive services delivered.

The specific aims for this project are to:

  • Determine the effectiveness of a multi-component translational intervention on adoption of three strategies known to increase delivery of preventive services: nurse standing orders, a reminder/recall system (preferably PSRS), and special immunization and/or preventive services clinics. The intervention will include: a) performance feedback and benchmarking; b) training of clinicians and office staff in principles of effective preventive services (enhanced academic detailing by a physician opinion leader); c) practice enhancement assistants to facilitate office system changes; and d) an IT application that provides prompts and reminders to office staff, clinicians, and patients.
  • Document contextual factors and barriers to the adoption of the three strategies and their impact on the intervention.
  • Measure the impact of the intervention on rates of delivery of the following preventive services: DtaP#4, MMR#1, and HepB#3 in 2-3 year olds, and pneumococcal immunization, colorectal cancer screening, and mammography in adults 50 - 75 years of age.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Primary care physician
  • Member of the Oklahoma Physicians Resource/Research Network
  • Computer with internet connection
  • More than 30 patients seen per week
  • Provides care to 2-3 year-olds and/or 50-75 year olds

Exclusion criteria

  • Does not provide preventive services
  • Inclusion of more than two of the preventive service delivery strategies at baseline
  • Involved in another network project
  • Unwilling to work with an external practice facilitator
  • IRB used by the practice will not allow records audits without individual patient consent

Treatment and study plan

Practice intervention

Other

Performance feedback, academic detailing, practice facilitation, IT support

Practice intervention 2

Other

Performance feedback only.

Primary outcomes

  1. Implementation of one or more of three evidence-based strategies

    Time frame: 6 months

Secondary outcomes

  1. Rates of delivery of selected preventive services

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

Agency for Healthcare Research and Quality (AHRQ)

Fed

Registry information

Important dates

Study start
2004
Primary completion
2006
Study completion
2006
First posted
Jun 24, 2005
Registry last updated
Aug 12, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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