|
|
||||||||
About Practice-Based Research Network |
From the American Academy of Family Physicians National Research Network, Leawood, KS
Correspondence: Corresponding author: Deborah G. Graham, MSPH, American Academy of Family Physicians, National Research Network, 11400 Tomahawk Creek Pkwy, Leawood, KS 66211 (E-mail: dgraham{at}aafp.org)
| Abstract |
|---|
|
|
|---|
The history of primary care PBRNs in the United States began in the 1970s, with the appearance of the earliest regional networks.2,3 In 1978, the creation of a national family medicine PBRN was set in motion, leading to development of the Ambulatory Sentinel Practice Network (ASPN). The AAFP NRN was established in 2000 to replace ASPN as the national family medicine PBRN.4,5 Since the AAFP NRN's inception, primary care PBRNs have grown significantly in size and number. The growth of PBRNs over the past 2 decades has been supported by a number of funding opportunities from the Agency for Healthcare Research Quality (AHRQ) specifically directed toward primary care PBRNs.6 In 2004, AHRQ identified 111 primary care PBRNs operating in the United States.3,6,7
PBRNs emphasize a close collaboration between practicing clinicians and researchers.1 Engaging network members in reflective inquiries can lead to practice improvement as well as new researchable questions for the network.8 However, the engagement of busy practices in practice-based research along with its growth in popularity and complexity of studies have led to increasing challenges in planning and implementing research studies in busy practices. Key challenges in this process include selecting studies that meet the goals and objectives of the network and its members; creating a practical, accurate, and sufficient study budget; developing study teams and agreements between team members; recruiting and selecting study sites; and training the practice staff for participation in network studies.912
AAFP NRN membership includes approximately 350 clinicians and study coordinators from 180 practices in 50 states and Canadian provinces. To date, the AAFP NRN has completed data collection in 17 studies and is currently working on 8 active projects. AAFP NRN studies range from simple physician surveys to complex randomized control trials and have included studies on topics such as bioterrorism preparedness of family physicians,13 patient safety in family physician offices,1420 diabetes,21 alcohol screening,22 patient communication, practice change, and depression screening and care.
In this study, we discuss the 5 strategies that have been developed in the AAFP NRN through an iterative process of adjusting and improving procedures to plan and launch new studies. We expect that these processes and procedures, as well as the lessons that we have learned, will be useful for both new and experienced networks interested in successfully implementing PBRN studies.
| Selecting Fundable, Feasible Studies |
|---|
|
|
|---|
|
If the senior leadership agrees that the idea meets these 4 criteria, a 1-page concept overview is presented to 1 of the 2 AAFP NRN Scientific Review Committees (SRC). Each SRC consists of 6 AAFP NRN physicians and 1 study coordinator (usually a nurse or medical assistant). Proposals are distributed to the 2 SRCs on a rotating basis. The SRCs objective is to determine whether the study proposal is suitable and feasible in a primary care practice. SRC members may also make suggestions on a studys methodology to enhance its implementation in a busy family medicine practice. The physician serving as committee chair is responsible for collecting committee member input and transmitting the final decision back to the AAFP NRN leadership.
Next, we assess the interest of the AAFP NRN membership. This process occurs before practice recruitment to validate that there is sufficient member interest in a particular study topic to meet recruitment goals. An AAFP NRN staff member communicates with network members who are appropriate for a given study, provides them with a 1-page overview of the study concept and a description of the responsibilities of the clinician or practice, and requests that they let us know if they are potentially interested in participating.
After a study idea progresses to this point in the process, the senior management begins developing a complete study protocol and pursuing funding options. Ultimately, it is the final decision of the AAFP NRN leadership and staff as to whether a project will proceed. However, because the success of network studies is contingent on participation of members, we strive to assure that they have ample input into the design of a research project early in the process.
The AAFP NRN developed its Principles for Industry-Funded Research (available at www.aafp.org/natnet) to guide negotiations with potential external commercial funders who invite the AAFP NRN to collaborate or take the lead on protocol development. This document outlines the principles by which the NRN collaborates with such industry sponsors, and clarifies the roles of both the AAFP NRN and the intended funders in the development, data collection, analysis, and dissemination of the research project.
| Creating a Practical Budget |
|---|
|
|
|---|
Depending on the funding source, a draft budget is either submitted for approval in the case of commercial and most private philanthropic funding or, in the case of government-sponsored funding, reviewed to determine whether the proposed budget fits into the funders allotment for the project. If the budget exceeds the available funds, the AAFP NRN director will make adjustments that ensure the project can be conducted without compromising the integrity of the study.
| Composing the Study Team |
|---|
|
|
|---|
|
The AAFP NRN has developed policies and procedures to standardize network operations. These policies strengthen the understanding of the research team, expedite our work, and eliminate future misunderstandings. In addition, we have developed model agreements designed to ensure a common understanding between the AAFP NRN and outside research team members. All the policies and agreements listed below are available at www.aafp.org/natnet.
"Writing Process for Manuscripts" includes the roles, expectations, timelines, and procedures for writing papers related to studies conducted in the AAFP NRN. This writing process was developed to facilitate the timely dissemination of research findings to practices and to the academic press. This agreement states that the AAFP NRN expects to publish the results of every study conducted in our network.
The Publication Policy outlines how investigators working with the AAFP NRN are to prepare manuscripts for primary and secondary publication. It covers topics such as authorship, manuscript preparation and titles, conflict resolution, and acknowledging the AAFP NRN and study sites in published papers.
The External PI Agreement provides a detailed description of the relationship between the AAFP NRN and PIs who are not staff of the AAFP. It clarifies that any projects brought to the network by external PIs must be consistent with the AAFP NRN's mission, objectives, and current research agenda. The document also outlines the development of project budgets, AAFP NRN policies for day-to-day project operations, financial responsibilities and authority of the AAFP NRN director, and expectations for the dissemination of findings.
The Data Sharing Agreement sets forth the terms, conditions, and obligations concerning data sharing between the AAFP NRN and any another network or person. It clarifies that if the AAFP NRN conducts a study resulting in a project dataset, then it owns such data.
The General Affiliation Agreement asserts that the AAFP NRN is interested in promoting collaborative arrangements with state and regional networks. It also delineates the conditions under which the AAFP NRN and regional networks can collaborate, including study selection, decision making, data collection, and IRB approval for collaborative studies.
| Recruiting and Selecting Sites |
|---|
|
|
|---|
In situations where AAFP NRN members will not provide adequate numbers, a decision is made whether affiliated state or regional networks will be invited to participate. The AAFP NRN staff generally works with affiliate network directors or administrators to identify members of those networks who may be appropriate for the study.
Once the recruitment strategy is developed, the project staff initiates the recruitment process. The chronology of practice recruitment and selection from AAFP NRN practices is generally the following:
We select practices from the pool of eligible and interested practices that meet inclusion criteria and maximize diversity based on geographic location, practice type, size, and any other pertinent characteristics. We also consider other factors such as whether a practice is already participating in another study, and a practice and study coordinators previous experience in network studies (in particular, if we are selecting practices for a more complex study). We have created a database to assist us in practice selection in which we store these data on all AAFP NRN member practices, physicians, and study coordinators.
For each participating practice, the lead physician, study coordinator, Practice Signatory Official (as designated by the practice), and the study PI sign a Practice Agreement. This document states that the practice agrees to carry out all designated responsibilities of the study and the AAFP NRN agrees to provide materials, provide and pay for training, and provide the designated stipend. Institutional Review Board (IRB) issues are spelled out in the Unaffiliated Investigator Agreement.
At times during the recruitment phase we must make tough decisions about balancing scientific rigor with the realities of "real-world" medical practice. For example, occasionally we are forced to modify the initial sampling plan to achieve the required sample size. In a recent study, we initially planned to include few residency practices. However, an eligibility requirement that a practice either had to deliver at least 50 babies or perform 50 well-baby visits in the previous year forced us to change our original recruitment strategy and include residency practices to get sufficient numbers for our study. In addition, although in an ideal world we would have the luxury of randomly selecting practices to increase the representativeness of our sample, this is not always possible in PBRN studies. Sometimes we need to include all interested practices to reach sample size requirements. Finally, although a study design may require equal numbers of practices with or without a particular characteristic (eg, those with and without electronic medical records), we sometimes learn after a study begins that a practice, in fact, did not really have that characteristic. Thus, when the budget permits, we oversample practices just as we oversample patients. For instance, if a study is randomized at the practice level and the power analysis indicates that 10 practices per arm are sufficient, we plan for attrition by budgeting for 12 practices per arm.
| Training Practice Staff and Physicians |
|---|
|
|
|---|
The entire research team, including all investigators, consultants, project manager, and research assistants, conducts the weekend sessions. The sessions have evolved into both a successful strategy for implementing studies in practices and a place where the practices make significant contributions that improve the design and feasibility of study protocols. Discussions encourage brainstorming on best strategies for implementing the protocol in a practice. As mentioned previously, practice leadership provides a new perspective, which frequently leads to improved protocol design and implementation, and ultimately to high quality study data.27
Training sessions also provide the opportunity for site leaders and the research team to get to know one another. In contrast to many regional networks, our national staff has few opportunities to meet face-to-face with members. Training sessions may be the only time during the study period that the research team and practice staff meet. These personal connections between the practice members and the research team lead to better communication throughout the study period and eventually lead to a more successful research study.
When key personnel from study sites are unable to attend the face-to-face training, we provide telephone training or ask someone who did attend the training to orient those who did not. However, these techniques cannot replicate the experience of a face-to-face training weekend with all the practices.
In addition, we develop an in-depth training manual that includes copies of and instructions for completion of all forms; the AAFP IRB application; all consent forms; instructions for completion of human subjects training; contact information for the central research team, practice physicians, practice study coordinators, and other key people; the study protocol, as appropriate; suggestions for study implementation, including recruitment and consent process for subjects; and other pertinent information. The manual is the basis of the training curriculum and agenda. A template for the manual and schedule appears in Table 2.
|
After training, practice participants and the research staff are generally excited and motivated to implement the study. To preserve the momentum generated from the training, we try to minimize the time between training and implementation in practices. However, this is not always possible for reasons such as if numerous changes to the protocol are made as a result of feedback from training participants; if practices need to train their staff and physicians before study initiation; or if practice-specific implementation strategies need to be developed. In cases where there is an extended period of time between the training session and study implementation in the practice, we conduct one-on-one refresher telephone calls with the study coordinator or the lead physician before the start of data collection.
| Conclusion |
|---|
|
|
|---|
| Acknowledgments |
|---|
| Notes |
|---|
|
|
|---|
Conflict of interest: The authors are employees of (DG, TS, MS, WP) or partially paid by (ES) the American Academy of Family Physicians.
Received for publication June 21, 2006. Accepted for publication December 18, 2006.
| References |
|---|
|
|
|---|
This article has been cited by other articles:
![]() |
E. Hummers-Pradier, C. Scheidt-Nave, H. Martin, S. Heinemann, M. M Kochen, and W. Himmel Simply no time? Barriers to GPs' participation in primary health care research Fam. Pract., April 15, 2008; (2008) cmn015v1. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. H. Gilbert, O. D. Williams, D. B. Rindal, D. J. Pihlstrom, P. L. Benjamin, M. C. Wallace, and for the DPBRN Collaborative Group The Creation and Development of the Dental Practice-Based Research Network J Am Dent Assoc, January 1, 2008; 139(1): 74 - 81. [Abstract] [Full Text] [PDF] |
||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | CONTACT US | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |