Trial of Positive Deviance in Inpatient Wards to Reduce Hospital Infections
NCT ID: NCT02244905
Last Updated: 2020-03-17
Study Results
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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COMPLETED
NA
16876 participants
INTERVENTIONAL
2011-08-31
2014-08-31
Brief Summary
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Detailed Description
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Design: A cluster randomized controlled trial was conducted over a period of 24 months. Six medical wards were randomized and positive deviance intervention was randomly allocated to one of the two groups of three wards each. The baseline, intervention and follow-up periods were 6, 9 and 9 months respectively.
Setting: A public safety-net major teaching hospital in United States.
Participants: The ward staffs participated in the intervention.
Intervention: Key components of the intervention were invitation to participate voluntarily, open-ended dialogues with staff members to discover barriers and seek solutions to prevent HAI, discussion of outcomes, and encouragement to prioritize and implement the solutions generated. Staffs of all six wards were asked to voluntarily participate in a modified hospital survey of patient safety climate (HSOPSC) and a social network survey at 6, 15, and 24 months.
Statistical analysis: Statistical methods used were time series modeling, summary of frequencies, Chi-square or Fisher's exact for testing difference in proportions and t-test.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
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Positive Deviance Intervention Arm
Three hospital wards received Positive Deviance intervention.
Positive Deviance
The recipients of the Positive Deviance intervention are the staff members of the three wards in the intervention arm, while the outcomes are measured among the patients receiving care in the three wards in the intervention arm. Key components of the intervention were invitation to participate voluntarily, open-ended dialogues with staff members to discover barriers and seek solutions to prevent HAI, discussion of outcomes, and encouragement to prioritize and implement the solutions generated.
Standard-of-Care Infection Control approach
Standard-of-Care Infection Control approach
Control Arm
Three hospital wards randomized to control arm received the Standard-of-Care Infection Control approach.
Standard-of-Care Infection Control approach
Standard-of-Care Infection Control approach
Interventions
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Positive Deviance
The recipients of the Positive Deviance intervention are the staff members of the three wards in the intervention arm, while the outcomes are measured among the patients receiving care in the three wards in the intervention arm. Key components of the intervention were invitation to participate voluntarily, open-ended dialogues with staff members to discover barriers and seek solutions to prevent HAI, discussion of outcomes, and encouragement to prioritize and implement the solutions generated.
Standard-of-Care Infection Control approach
Standard-of-Care Infection Control approach
Eligibility Criteria
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Inclusion Criteria
* For Primary Outcome Assessment:
* All patients admitted to any of the six study wards included in the study over the 24-month study period.
Exclusion Criteria
ALL
No
Sponsors
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University of Texas Southwestern Medical Center
OTHER
Responsible Party
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Principal Investigators
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Pranavi Sreeramoju, MD
Role: PRINCIPAL_INVESTIGATOR
UT Southwestern Medical Center
Other Identifiers
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Grant # 137911
Identifier Type: OTHER
Identifier Source: secondary_id
STU 072011-079
Identifier Type: -
Identifier Source: org_study_id
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