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Clinical Trial Details — Status: Unknown status

Administrative data

NCT number NCT01255488
Other study ID # R02930-S2
Secondary ID
Status Unknown status
Phase N/A
First received December 6, 2010
Last updated December 6, 2010
Start date December 2010
Est. completion date June 2011

Study information

Verified date November 2010
Source Uniformed Services University of the Health Sciences
Contact Ronald W Gimbel, PhD
Phone 301-295-3077
Email rgimbel@usuhs.mil
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To better understand the extent to which family nurse practitioners (FNPs) might use research abstracts in shaping their clinical decision-making under simulated conditions. A secondary point is to examine if and how FNPs might use full-text manuscripts (associated with the abstracts) if made available to them.


Description:

The study will recruit the approximate 25 - 1st year and 25 - 2nd year family nurse practitioner students of the Graduate School of Nursing. After being presented an overview of the study and informed consent document, those electing to participate will draw a sealed envelope indicating whether they are assigned to group A (intervention group) or group B (control group). The participant will proceed to the associated room, be provided a brief clinical case (appropriate to their training), an iPad device with pre-loaded EBN-Search engine, and a questionnaire. The EBN-Search engine for the intervention group will include 9 research abstracts associated to the case. The EBN-Search for the control group will include both the research abstracts and full-text versions of the manuscripts. The participants will be provided 20 minutes to complete the questionnaire using the information available to them. The questionnaire will require the participant to indicate treatment plan, respond to questions regarding the usefulness of research abstracts, questions regarding the usefulness of full-text (control group only) and recommendations on improving EBN-Search.


Recruitment information / eligibility

Status Unknown status
Enrollment 50
Est. completion date June 2011
Est. primary completion date March 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria:

- Matriculated family nurse practitioner graduate students of USUHS 2010/2011 academic year

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Access to EBN-Search (without full-text manuscripts)
Family nurse practitioner access to EBN-Search without availability of full-text manuscripts.

Locations

Country Name City State
United States Uniformed Services University Bethesda Maryland

Sponsors (1)

Lead Sponsor Collaborator
Uniformed Services University of the Health Sciences

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Measure of perception of abstract usefulness in clinical decision-making At conclusion of the simulated exercise subjects will complete a data collection instrument indicating their perception of abstract usefulness in their clinical decision-making. Immediate post-experiment
Secondary Use of full-text manuscripts when available in simulated clinical encounter For those subjects with ready access to full-text manuscripts (n=25) during the simulated clinical encounter, we will measure how often they are accessed by the subjects. During experiment
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