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Clinical Trials/NCT02752165
NCT02752165
Completed
Not Applicable

Telemedicine Enhanced Asthma Management Through the Emergency Department

University of Rochester1 site in 1 country384 target enrollmentDecember 15, 2016
ConditionsAsthma

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Asthma
Sponsor
University of Rochester
Enrollment
384
Locations
1
Primary Endpoint
Number of Symptom-Free Days in the Prior 2 Weeks
Status
Completed
Last Updated
7 months ago

Overview

Brief Summary

In the US, children from minority ethnic and racial backgrounds suffer disproportionately from asthma and account for substantially more emergency department (ED) visits and hospitalizations than non-minority children. While NHLBI guidelines recommend daily preventive medications for all children with persistent asthma to prevent morbidity as well as ED visits and hospitalizations, many children who should receive preventive medications are not receiving them. This is in part because children presenting to the ED for an acute asthma exacerbation rarely receive preventive asthma care, due to the ED's focus on acute, episodic care. The NHLBI guidelines recommend that children follow-up with a primary care provider (PCP) within 1-4 weeks of the ED visit. The post-ED follow-up visit is an opportunity for the PCP to prescribe effective preventive asthma medications, step-up medication for children who demonstrate poor control, promote adherence, and provide education on asthma self-management and trigger control. However, rates for follow-up after an asthma-related ED visit are extremely low, and preventive care is delivered inconsistently even when children are seen in follow-up. In the investigators' prior work they have found that a provider prompting intervention can enhance the delivery of guideline-based preventive asthma treatments at the time of a primary care office visit and ultimately reduce morbidity. They have also found that telemedicine can link children with persistent asthma to a provider for optimal chronic illness management. The goal of this project is to use a novel telemedicine-based program to facilitate primary care follow-up and promote the delivery of guideline-based preventive care for high-risk children presenting to the ED for an asthma exacerbation. The investigators will utilize a 2-group randomized trial to test the TEAM-ED intervention. The intervention includes: 1) a telemedicine assessment at the child's school within one week of discharge from the ED and completed by a PCP, 2) 'point-of-care' prompting to promote the provision of guideline-based preventive care during the telemedicine visit, and 3) two additional telemedicine-assisted follow-up assessments to assure optimal response to treatment and tailor the care regimen as needed. The investigators will assess the effectiveness of the program in reducing respiratory morbidity and improving preventive asthma care, with follow-up assessments at 3, 6, 9, and 12 months.

Registry
clinicaltrials.gov
Start Date
December 15, 2016
End Date
July 12, 2022
Last Updated
7 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jill Halterman

Professor

University of Rochester

Eligibility Criteria

Inclusion Criteria

  • Prior physician diagnosis of asthma
  • current emergency visit for an acute asthma exacerbation, requiring nebulized albuterol therapy
  • Persistent or poor control of asthma, defined by NHLBI guidelines

Exclusion Criteria

  • Inability to speak and understand either English or Spanish
  • No access to a phone for follow-up surveys
  • Participation in another asthma study at the time of enrollment, or a sibling participating in this or another study Other significant medical conditions that could interfere with assessment of asthma-related measures
  • children in foster care or other situations in which consent cannot be obtained from a legal guardian

Outcomes

Primary Outcomes

Number of Symptom-Free Days in the Prior 2 Weeks

Time Frame: At the 12-month follow-up assessment

Number of days without symptoms in the prior 2 weeks

Study Sites (1)

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