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Completed

NCT Number: NCT03777241

Disruptive bEhavior manageMEnt ANd Prevention in Hospitalized Patients Using a behaviORal Intervention Team

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Vanderbilt University Medical Center

Nashville, Tennessee, 37212, United States

About this study

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:

  • meaningful, measureable improvement in the prevention and management of disruptive behavior in the healthcare setting at VUMC, and
  • 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:

  • Improvement in the prevention and management of patients exhibiting disruptive, threatening or acting out behavior
  • Improvement in staff perceptions of their ability to manage patients exhibiting disruptive, threatening or acting out behavior

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Behavioral Intervention Team

Behavioral

Multidisciplinary team to assist with actively identifying and managing mental illness and substance abuse disorders at their earliest possible time during hospitalization.

Standard of Care

Behavioral

Participants in this group will receive standard of care.

Primary outcomes

  1. Percent of violence control measures utilized

    Time frame: 6 months

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

  2. Percent of patient injurious behaviors reported

    Time frame: 6 months

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

  3. 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

  1. Rate of unit nursing staff retention

    Time frame: 1 year

    By extracting rates from internal human resources records

  2. Patient length of stay

    Time frame: 6 months

    By extracting data from the electronic health record

Sponsors and collaborators

Lead sponsor

Vanderbilt University

Other

Collaborators

  • Vanderbilt University Medical Center

Registry information

Official study title

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

Acronym: DEMEANOR

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Dec 17, 2018
Registry last updated
Sep 9, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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