Aggressive Incidents in Medical Settings Study

NCT ID: NCT03041272

Last Updated: 2020-03-06

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

Total Enrollment

137 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-01-31

Study Completion Date

2017-11-30

Brief Summary

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The purpose of this study is to identify the incidence rate and characteristics of aggressive behavior perpetrated by patients and visitors in inpatient medical units and to understand the role of missed care events, professional quality of life and self-efficacy in relationship to aggressive events.

Detailed Description

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This prospective cohort study will examine the incidence of and outcomes associated with patient and visitor aggressive behavior towards nursing staff practicing on medical inpatient units. Staff on each unit will be informed about the AIMS study and all eligible nursing staff will be invited to participate in the study. After completing the informed consent nursing staff will be asked to complete the baseline demographic form and survey on professional quality of life. For the data collection phase of the study consented participants will be educated on use of the AIM log and provided with scenarios to practice AIM log use. Consented staff will carry event counters and use the AIM log for all shifts worked over the next 2 weeks.

Conditions

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Aggression

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Nurses and nursing personnel

All registered nurses and assistive nursing personnel, including patient care associates (PCAs) , patient care technicians (PCTs), clinical technicians (CTs), primary employment on the study unit, minimum of 24 hours per week of employment on study unit.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* All registered nurses and assistive nursing personnel, including patient care associates (PCAs) , patient care technicians (PCTs), clinical technicians (CTs),
* primary employment on the study unit,
* minimum of 24 hours per week of employment on study unit.

Exclusion Criteria

* Any registered nurse or assistive nursing personnel working less than 24 hours per week,
* whose primary employment is on a unit not involved in the study or float-pool / centralized resource staff who do not have a primary employment unit,
* any nursing staff member still on orientation or working with an orientee.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Yale University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Joanne Iennaco

Role: PRINCIPAL_INVESTIGATOR

Yale School of Nursing

Locations

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Middlesex Hospital

Middletown, Connecticut, United States

Site Status

Yale New Haven Hospital- St. Raphael

New Haven, Connecticut, United States

Site Status

Yale New Haven Hospital Primary Care Center

New Haven, Connecticut, United States

Site Status

Countries

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United States

Other Identifiers

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1609018379

Identifier Type: -

Identifier Source: org_study_id

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