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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03204643
Other study ID # 00021808
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 12, 2017
Est. completion date March 31, 2018

Study information

Verified date January 2020
Source Wake Forest University Health Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients who present to one of the participating EDs with a telepsychiatric consult performed will be treated and followed per the behavioral health virtual patient navigation pathway (BH-VPN) or usual care. The BH-VPN is inclusive of several components which will all be consistently applied to patients randomized to the intervention, as well as having access to behavioral health trained patient navigators. These key components are often deployed inconsistently as a part of usual care, but per the intervention, will be completed in totality for subjects who are assigned to and participate in the BH-VPN plan. This study includes a qualitative sub-study to measure perceptions of the impact of the BH-VPN on readmission rates and patient outcomes, experiences with the services provided by the BH-VPN, and provider and clinician ideas for how to improve the services provided by the BH-VPN.


Recruitment information / eligibility

Status Completed
Enrollment 637
Est. completion date March 31, 2018
Est. primary completion date February 14, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Present at a participating ED - Completed telepsychiatric consult as captured in the EMR - Completed telepsychiatric consult Monday - Friday during Navigator's potential hours of operation. Exclusion Criteria: - None per the protocol

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
BH-VPN
A bundle of usual care components, applied consistently and completely, along with access to behavioral health specific patient navigators and navigation services.

Locations

Country Name City State
United States Carolinas Healthcare System - Pineville Charlotte North Carolina
United States Carolinas Healthcare System Steele Creek Charlotte North Carolina
United States Carolinas Healthcare System University Charlotte North Carolina
United States Carolinas Medical Center Mercy Charlotte North Carolina
United States Carolinas Healthcare System Huntersville Huntersville North Carolina
United States Carolinas Healthcare System - Union Monroe North Carolina

Sponsors (1)

Lead Sponsor Collaborator
Wake Forest University Health Sciences

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Emergency Department to Inpatient Conversion Rate admission from the Emergency Department with behavioral health consult completed, to an inpatient or observation setting. 5 days
Secondary Quality, Comfort, and Care (QCC) Defined Readmission Rate readmission within 30 days to the same facility 30 days
Secondary Patient-centric (Protocol Defined) Readmission Rate readmission within 30 days to any facility which Carolinas Healthcare System have access to the data 30 days
Secondary Utilization of Healthcare Services Post-discharge From Emergency Department Number of Emergency Department, inpatient, observation encounters 45 days
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