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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01168323
Other study ID # M15310
Secondary ID IRB# 17865K08HS0
Status Completed
Phase N/A
First received July 20, 2010
Last updated August 6, 2010
Start date January 2007
Est. completion date February 2009

Study information

Verified date July 2010
Source Harvard University Faculty of Medicine
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Two memory research findings (the spacing and testing effects) can dramatically improve retention of learning, but they have largely have been ignored by educators. The researchers have developed a novel form of online education (termed 'spaced education') based on these two effects which has been shown in randomized trials to improve knowledge acquisition and boost learning retention. Using prostate cancer screening as an experimental system, the researchers investigated whether spaced education could durably improve clinicians' behaviors, not just their knowledge.


Recruitment information / eligibility

Status Completed
Enrollment 95
Est. completion date February 2009
Est. primary completion date February 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Primary care providers (physicians, nurse practitioners, and physician assistants) from the 8 Veterans Affairs (VA) hospitals in the New England region (Veterans Integrated Service Network 1 [VISN-1]) were eligible to enroll.

Exclusion Criteria:

- Primary care providers (PCPs) who ordered PSA as a screen for prostate cancer less than 10 times each year were excluded.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Behavioral:
Online spaced education
Spaced education is currently delivered via periodic emails that contain clinical case scenarios and multiple-choice questions. Upon submitting answers to each question online, clinicians receive immediate feedback and educational material. The questions are then repeated over spaced intervals of time to harness the pedagogical benefits of the spacing effect.

Locations

Country Name City State
United States Veterans Affairs Boston Healthcare System Boston Massachusetts

Sponsors (7)

Lead Sponsor Collaborator
Harvard University Faculty of Medicine Agency for Healthcare Research and Quality (AHRQ), American Urological Association, Astellas Pharma US, Inc., National Institutes of Health (NIH), VA Office of Research and Development, Wyeth is now a wholly owned subsidiary of Pfizer

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of inappropriate prostate-specific antigen (PSA) screening performed by clinicians The primary outcome measure was the difference in the percentage of inappropriate PSA screening performed by clinicians in the spaced education and control cohorts. Based on published clinical guidelines and reports, inappropriate PSA utilization was defined as the use of PSA for prostate cancer screening in patients >76 or <40 years old, or with an estimated life expectancy of less than 10 years. Weeks 1-108 No
Secondary Change in test scores between cohorts measured in weeks 1-36 Weeks 1-36 No
Secondary Change in spaced education performance measured in weeks 1-36 Weeks 1-36 No
Secondary Clinicians' intention to participate in future spaced education programs Assessed on end-of program survey at week 36 Week 36 No
Secondary Time required by clinicians to complete the spaced education questions-explanations Assessed on end-of program survey at week 36 Week 36 No
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