Improved Adherence to C. Difficile Isolation Protocols Through Improved Education Methods

NCT ID: NCT02375477

Last Updated: 2018-01-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

38 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-01-27

Study Completion Date

2018-01-06

Brief Summary

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This clinical trial studies how well inter-disciplinary educational methods work in improving adherence to isolation protocols in patients with Clostridium (C.) difficile infections. An inter-disciplinary educational method may help to prevent the spread of infection.

Detailed Description

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PRIMARY OBJECTIVES:

I. To lower rates of C. difficile transmission through improved adherence to recommended isolation protocols.

SECONDARY OBJECTIVES:

I. Improve resident knowledge of infection control procedures and engagement in quality improvement initiatives.

OUTLINE:

Residents and nurses are given a short presentation on isolation protocols for diarrhea and enteric pathogens approved by Infection Control and covering their recommendations.

After completion of study, residents and nurses complete post-tests to determine the effectiveness of the training every 6 months.

Conditions

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Bacterial Infection Clostridium Difficile

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

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Health services research (isolation protocol education)

Residents and nurses are given an educational intervention on isolation protocols for diarrhea and enteric pathogens approved by Infection Control and covering their recommendations.

Group Type EXPERIMENTAL

Educational Intervention

Intervention Type OTHER

Given educational presentation

Interventions

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Educational Intervention

Given educational presentation

Intervention Type OTHER

Other Intervention Names

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Education for Intervention Intervention, Educational

Eligibility Criteria

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Inclusion Criteria

* Patient on the gynecologic oncology service
* Admitted to Seidman 6th floor of the Seidman Cancer Center
* Diarrhea or clinical concern for C. difficile infection


* Any resident or nurse treating a patient meeting the above criteria

Exclusion Criteria

* None

Medical Staff Criteria:


* None
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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National Cancer Institute (NCI)

NIH

Sponsor Role collaborator

Case Comprehensive Cancer Center

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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John Nakayama

Role: PRINCIPAL_INVESTIGATOR

Case Comprehensive Cancer Center

Locations

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Case Comprehensive Cancer Center

Cleveland, Ohio, United States

Site Status

Countries

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United States

Other Identifiers

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NCI-2015-00147

Identifier Type: REGISTRY

Identifier Source: secondary_id

CASE1815

Identifier Type: OTHER

Identifier Source: secondary_id

P30CA043703

Identifier Type: NIH

Identifier Source: secondary_id

View Link

CASE1815

Identifier Type: -

Identifier Source: org_study_id

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