ETOC: Trial of Emergency Department Discharge With Enhanced Transitions of Care Compared to Usual Care

Sponsor
Thomas Jefferson University (Other)
Overall Status
Completed
CT.gov ID
NCT02533856
Collaborator
(none)
316
2
9

Study Details

Study Description

Brief Summary

This is a randomized controlled trial to assess the relative effectiveness of providing Enhanced Transitions of Care (ETOC) to improve patient outcomes after discharge from the Emergency Department (ED). Patients who are being discharged from the ED and have had a previous ED visit or hospital admission within the Thomas Jefferson Hospital System (TJUH or Methodist) within the past 90 days will be eligible for enrollment in this trial. Patients who consent to enrollment will be randomized to discharge by usual care or discharge with ETOC as provided by the company BoardRounds.

Condition or Disease Intervention/Treatment Phase
  • Other: ETOC
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
316 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Randomized Control Trial of Emergency Department Discharge With Enhanced Transitions of Care Compared to Usual Care
Study Start Date :
Aug 1, 2015
Actual Primary Completion Date :
May 1, 2016
Actual Study Completion Date :
May 1, 2016

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Usual Care

Discharge from emergency department by usual care

Experimental: ETOC

Discharge from emergency department with increased support services provided by BoardRounds after ED discharge

Other: ETOC
Services provided to assist patients in accessing needed healthcare services after emergency department discharge such as scheduling appointments, finding new doctors, getting medications, or addressing problems with insurance coverage.

Outcome Measures

Primary Outcome Measures

  1. Total number of ED visits, hospital admissions, and outpatient office visits as determined by medical record review and patient report [30 days]

    30-day healthcare utilization will be measured by assessing the total number of ED treat-and-release visits, hospital admissions, and outpatient care visits in the 30 days after study enrollment - will be reported in aggregate and separately for each type of utilization (ED, inpatient hospital stay, office visit). Counts will be determined by medical record review for visits occurring within the health system, and will be supplemented by patient report in a 30-day survey to determine utilization outside the health system.

Secondary Outcome Measures

  1. Total number of ED visits, hospital admissions, and outpatient office visits as determined by medical record review and patient report [9 days]

    9-day healthcare utilization will be measured by assessing the total number of ED treat-and-release visits, hospital admissions, and outpatient care visits in the 30 days after study enrollment - will be reported in aggregate and separately for each type of utilization (ED, inpatient hospital stay, office visit). Counts will be determined by medical record review for visits occurring within the health system, and will be supplemented by patient report in a 30-day survey to determine utilization outside the health system.

  2. Description of types of and count (per type) of assistance received by patients in accessing needed healthcare services as assessed by patient survey [30 days]

    Patients will be surveyed at 30 days to determine the types of assistance received, and frequency with which each type was received, in accessing needed healthcare services since their discharge from the ED.

  3. Description of types of and count (per type) of assistance received by patients in accessing needed healthcare services as assessed by patient survey [9 days]

    Patients will be surveyed at 30 days to determine the types of assistance received, and frequency with which each type was received, in accessing needed healthcare services since their discharge from the ED.

  4. Assessment of whether patient had unmet needs in accessing needed healthcare services, as determined by patient survey [30 days]

    Determination of whether patient had unmet needs (yes/no) in accessing needed healthcare services in the 30-days after ED discharge as identified by patient in a survey administered at 30 days post-discharge.

  5. Assessment of whether patient had unmet needs in accessing needed healthcare services, as determined by patient survey [9 days]

    Determination of whether patient had unmet needs (yes/no) in accessing needed healthcare services in the 9-days after ED discharge as identified by patient in a survey administered at 9 days post-discharge.

Other Outcome Measures

  1. Description of unmet needs in accessing needed healthcare services as assessed in a patient survey [30 days]

    This will be a descriptive outcome to describe the types and counts of unmet needs that are identified by patients in the 30-days after ED discharge, as assessed in a survey administered 30 days after discharge. There will not be statistical analysis performed on this outcome, rather it will be descriptive and exploratory regarding patient primary struggles after ED discharge.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Adult (18 yrs and older) patients

  • Have had a previous ED visit or hospital admission in the 90 days prior to the current ED visit (at Thomas Jefferson University Hospital or Methodist Hospital)

  • Have just completed evaluation in the Thomas Jefferson University Hospital Emergency Department for any problem,

  • Are ready for discharge from the Thomas Jefferson University Hospital ED, and

  • Provide informed consent

Exclusion Criteria:
  • Non-English speaking patients

  • Patients undergoing medical clearance for a detox center or any involuntary court or magistrate order

  • Patients who live outside Philadelphia area (unable to seek follow-up care in Philadelphia) or other condition known to preclude follow-up (such as no reliable access to a telephone)

  • Patients in police custody or currently incarcerated individuals

  • Patients who have, in their clinician's best judgment, major communication barriers such as visual or hearing impairment or dementia that would compromise their ability to give written informed consent

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Thomas Jefferson University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Thomas Jefferson University
ClinicalTrials.gov Identifier:
NCT02533856
Other Study ID Numbers:
  • 15G.242
First Posted:
Aug 27, 2015
Last Update Posted:
Oct 21, 2016
Last Verified:
Oct 1, 2016
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 21, 2016