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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03777241
Acronym
DEMEANOR
Enrollment
3800
Registered
2018-12-17
Start date
2019-03-01
Completion date
2020-05-11
Last updated
2020-09-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Behavioral Problem

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

Interventions

BEHAVIORALBehavioral Intervention Team

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

BEHAVIORALStandard of care

Participants in this group will receive standard of care.

Sponsors

Vanderbilt University Medical Center
CollaboratorOTHER
Vanderbilt University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Percent of violence control measures utilized6 monthsBy extracting medications, restraints, and sitters ordered from the electronic health records
Percent of patient injurious behaviors reported6 monthsBy 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 behavior1 yearBy administering surveys to participants

Secondary

MeasureTime frameDescription
Rate of unit nursing staff retention1 yearBy extracting rates from internal human resources records
Patient length of stay6 monthsBy extracting data from the electronic health record

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026