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Clinical Trials/NCT03777241
NCT03777241
Completed
Not Applicable

Disruptive bEhavior manageMEnt ANd Prevention in Hospitalized Patients Using a behaviORal Intervention Team: Study Protocol for a Pragmatic, Cluster, Cross-over Design

Vanderbilt University1 site in 1 country3,800 target enrollmentMarch 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Behavioral Problem
Sponsor
Vanderbilt University
Enrollment
3800
Locations
1
Primary Endpoint
Percent of violence control measures utilized
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The purpose of the proposed study is to evaluate the impact of a behavioral intervention team (BIT) on 2 adult units: a general medical (8N); a cardiac/medical stepdown (8S) at Vanderbilt University Medical Center (VUMC) with a higher proportion of patients with behavioral health comorbidities.

Detailed Description

The BIT will provide a proactive psychiatric team that will screen all patients on admission, provide consultation to those meeting established criteria, and recommend interventions to the primary care team for consideration. BIT will also serve to model therapeutics tactics in communication and goal setting to the clinical staff. Research Questions for the proposed study: Considering that behavioral health co-morbidity is common among hospitalized medical inpatients and is associated with higher costs of care and staff dissatisfaction, we will ascertain whether the addition of dedicated, trained behavioral intervention team, compared to nursing staff training on trauma informed care and de-escalation techniques provides: 1. meaningful, measureable improvement in the prevention and management of disruptive behavior in the healthcare setting at VUMC, and 2. Improvement in staff perceptions of their ability to manage patients exhibiting disruptive, threatening or acting out behavior Specifically, using a pragmatic, cluster cross-over trial design where the BIT crosses between 8N and 8S, we will test the hypothesis that presence of the BIT results in: 1. Improvement in the prevention and management of patients exhibiting disruptive, threatening or acting out behavior 2. Improvement in staff perceptions of their ability to manage patients exhibiting disruptive, threatening or acting out behavior

Registry
clinicaltrials.gov
Start Date
March 1, 2019
End Date
May 11, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ruth Kleinpell

Professor

Vanderbilt University

Eligibility Criteria

Inclusion Criteria

  • All patients admitted to two adult medical surgical units (8N/8S) at Vanderbilt University Medical Center during the study period.
  • All clinical nurses and staff on 8N/8S employed during the study period.

Exclusion Criteria

  • Patients admitted to the floor before the BIT team has begun the crossover period on the unit.

Outcomes

Primary Outcomes

Percent of violence control measures utilized

Time Frame: 6 months

By extracting medications, restraints, and sitters ordered from the electronic health records

Percent of patient injurious behaviors reported

Time Frame: 6 months

By extracting reports of biting, kicking, throwing, etc. from the electronic medical record

Percent change in nurse comfort and confidence in their ability to manage patients exhibiting disruptive, threatening or acting out behavior

Time Frame: 1 year

By administering surveys to participants

Secondary Outcomes

  • Rate of unit nursing staff retention(1 year)
  • Patient length of stay(6 months)

Study Sites (1)

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