CONDOR Impact of Dental Practice-Based Research Network (CONDOR PIRG)

June 14, 2011 updated by: Dental Practice-Based Research Network

CONDOR Impact of Dental Practice-Based Research Network (PIRG)

The purpose of this study was to study the use of a Core Questionnaire that included several questions from each PBRN (DPBRN, PEARL, PRECEDENT - collectively know as CONDOR) that had been extracted from questionnaires previously administered as part of their initial research program activities. This protocol was the first administration of this core questionnaire with the purpose of assessing dental practice changes that may have occured since the earlier administration of the individual questions with the separate networks.It also collected baseline data for others.

Study Overview

Status

Completed

Conditions

Detailed Description

The three dental PBRNs had a unique opportunity to measure the impact of research participation on potential changes in practice base of the research protocol. We were able to examine the effect of participation in research in general to the acceptance of research findings from other studies and the effect of association with but not participation in a research network.

Study Type

Observational

Enrollment (Actual)

687

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Denmark
      • Copenhagen, Denmark
        • University of Copenhagen Royal Dental College
  • United States
    • Alabama
      • Birmingham, Alabama, United States, 35294-0007
        • University of Alabama at Birmingham
    • Florida
      • Gainesville, Florida, United States, 32610
        • University of Florida College of Dentistry
    • Minnesota
      • Minneapolis, Minnesota, United States, 55440-1309
        • Health Partners Dental Group
      • Minneapolis, Minnesota, United States, 55440-1524
        • Health Partners Research Foundation
    • Oregon
      • Portland, Oregon, United States, 97227
        • Kaiser Permanente Center for Health Research
      • Portland, Oregon, United States, 97232
        • Permanente Denrtal Associates

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

22 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

The questionnaire was administered to all DPBRN practitioner-investigators (including both dentists and hygienists) 22 years of age or older.

Description

Inclusion Criteria:

  • DPBRN dentists and hygienists who had completed a DPBRN Enrollment questionnaire and for whom DPBRN had a current active address and who were currently licensed to practice
  • reported on the Enrollment Questionnaire they were a general dentist, pediatric dentist, or dental hygienist, or reported doing at least some restorative dentistry procedures
  • practiced in one of the five DPBRN regions (AL/MS, FL/GA, MN< PDA, or SK)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Measure impact of research participation

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Dental Practice-Based Research Network

Collaborators

National Institute of Dental and Craniofacial Research (NIDCR)
HealthPartners Institute
Kaiser Permanente
Permanente Dental Associates Group, Oregon

Investigators

  • Study Chair: Gregg H Gilbert, DDS, MBA, The University of Alabama at Birmingham

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2009

Primary Completion (Actual)

January 1, 2010

Study Completion (Actual)

January 1, 2010

Study Registration Dates

First Submitted

September 13, 2010

First Submitted That Met QC Criteria

September 13, 2010

First Posted (Estimate)

September 14, 2010

Study Record Updates

Last Update Posted (Estimate)

June 16, 2011

Last Update Submitted That Met QC Criteria

June 14, 2011

Last Verified

June 1, 2011

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 126171
  • U01DE016747 (U.S. NIH Grant/Contract)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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