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Pediatric Emergency Department Smartphone Otoscope Study (PED-Oto)

Primary Purpose

Acute Otitis Media, Acute Otitis Externa

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Smartphone otoscope
Conventional otoscope
Sponsored by
Emory University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Acute Otitis Media focused on measuring Pediatrics, Emergency Medicine, Ear infection

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Participants must be a pediatric emergency care clinicians providing care at an emergency department a participating children's hospital
  • Willing to agree to random assignment to either a smartphone otoscope device or a conventional otoscope device for the 6-month study period
  • Willing to log patient encounters that included the an otoscopic examination for non-traumatic indication for each shift
  • Willing to document and report episodes of care in which the assigned otoscopic device could not be used on a study-eligible otoscopic examination
  • Willing to complete an end of study assessment, if assigned to use the smartphone otoscope

Exclusion Criteria:

  • Declines to give informed consent to participate in the study

Sites / Locations

  • Children's Healthcare of Atlanta at Hughes Spalding
  • Children's Healthcare of Atlanta at Egleston

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Smartphone otoscope

Conventional otoscope

Arm Description

Participating clinicians randomized to the smartphone otoscope study arm will use a smartphone otoscope for all otic (ear) examinations for a 6-month period.

Participating clinicians randomized to the conventional otoscope study arm will use a conventional otoscope for all otic (ear) examinations for a 6-month period.

Outcomes

Primary Outcome Measures

Number of Antibiotic Prescriptions
The number of emergency department encounters where antibiotics were prescribed to treat acute otitis media (AOM) are presented here. Information about antimicrobial prescriptions were found in the medical records of children receiving an otoscopic exam by a participating clinician.

Secondary Outcome Measures

Number of Diagnoses of Acute Otitis Media (AOM)
The number of emergency department encounters where a diagnosis of acute otitis media (AOM) was made is presented here. Information about the diagnosis of AOM was found in the medical records of children receiving an otoscopic exam by a participating clinician.
Number of Diagnoses of Otitis Externa
The number of emergency department encounters where a diagnosis of otitis externa was made is presented here. Information about the diagnosis of otitis externa was found in the medical records of children receiving an otoscopic exam by a participating clinician.
Clinician Acceptability of the Smartphone Otoscopic Device
Clinicians randomized to use the smartphone otoscopic device completed a survey to assess the acceptability of this device compared to the historical use of a conventional otoscope. The survey, developed specifically for this study, asked clinicians to report on their preference for using the smartphone otoscope over the conventional otoscope, whether the device increased their ability to diagnose AOM, and the perceived impact on antibiotic prescribing.

Full Information

First Posted
September 28, 2016
Last Updated
June 18, 2018
Sponsor
Emory University
Collaborators
Georgia Institute of Technology, Children's Healthcare of Atlanta
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1. Study Identification

Unique Protocol Identification Number
NCT02918773
Brief Title
Pediatric Emergency Department Smartphone Otoscope Study (PED-Oto)
Official Title
Pediatric Emergency Department Smartphone Otoscope Study (PED-Oto)
Study Type
Interventional

2. Study Status

Record Verification Date
June 2018
Overall Recruitment Status
Completed
Study Start Date
October 15, 2016 (Actual)
Primary Completion Date
April 15, 2017 (Actual)
Study Completion Date
April 15, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Emory University
Collaborators
Georgia Institute of Technology, Children's Healthcare of Atlanta

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Acute otitis media (AOM), defined as acute inflammation in the middle ear, is a leading cause of health encounters and antimicrobial prescriptions in children worldwide. Diagnosis of AOM is often dependent on a brief view of the tympanic membrane in an uncooperative child's ear canal. As a consequence, AOM may be inappropriately diagnosed when visualization of the tympanic membrane (ear drum) is not optimal. Improved methods for visualizing the tympanic membrane including capturing still images and recording video of the ear exam would be beneficial in the diagnosis and management of otic complaints, including acute and chronic otitis media. Use of a smartphone otoscope has the potential to optimize clinician ability to manage otic complaints, visualize the tympanic membrane, and support antimicrobial stewardship. This study will be conducted as a randomized control study in two affiliated children's hospital emergency departments. Twenty volunteer clinicians will be randomly assigned to use either a smartphone otoscope or a conventional otoscope for all otic examinations for a 6-month period.
Detailed Description
A smartphone otoscope (CellScope-Oto) is a pocket size attachment that employs the technology and light source of a smartphone to capture reproducible images of the ear canal and tympanic membrane. Previous studies with this device demonstrated that images taken with both the smartphone otoscope and a camera-fitted conventional analogue otoscope were equivalent with respect to image quality and that the smartphone otoscope was acceptable as an educational and diagnostic tool to health professional students. A pilot study with a similar design to this study conducted in two offices of an ambulatory pediatric clinic demonstrated a trend toward decreased antimicrobial prescription filling among families whose children were examined with the smartphone otoscope compared to those who were examined with a conventional otoscope. To further assess this trend, this study proposes an evaluation of the impact of device use on antimicrobial prescribing for children with an otic complaint in a pediatric emergency department (PED) setting. This study will enroll 20 clinicians for the 6-month study period; 10 who will be randomly assigned to use a smartphone otoscope for the 6-month study period and 10 who will be assigned to use a conventional otoscope for all otoscopic exams. Data will be abstracted via retrospective review of the electronic medical record of encounters in with an otoscopic exam was performed as part of the diagnostic evaluation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Otitis Media, Acute Otitis Externa
Keywords
Pediatrics, Emergency Medicine, Ear infection

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
22 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Smartphone otoscope
Arm Type
Experimental
Arm Description
Participating clinicians randomized to the smartphone otoscope study arm will use a smartphone otoscope for all otic (ear) examinations for a 6-month period.
Arm Title
Conventional otoscope
Arm Type
Active Comparator
Arm Description
Participating clinicians randomized to the conventional otoscope study arm will use a conventional otoscope for all otic (ear) examinations for a 6-month period.
Intervention Type
Device
Intervention Name(s)
Smartphone otoscope
Other Intervention Name(s)
CellScope-Oto
Intervention Description
A smartphone otoscope is a pocket size smartphone attachment that uses the technology and light source of a smartphone to capture reproducible images of the ear canal and tympanic membrane. The smartphone otoscope has the capability to capture still images and video, which can be referred to post-examination as well as be incorporated into an electronic medical record. Clinicians will use the smartphone otoscope for the duration of the 6-month study period.
Intervention Type
Device
Intervention Name(s)
Conventional otoscope
Intervention Description
A conventional otoscope has a light and lenses to provide a view of the ear canal and tympanic membrane or eardrum. Clinicians will use the conventional otoscope for the duration of the 6-month study period.
Primary Outcome Measure Information:
Title
Number of Antibiotic Prescriptions
Description
The number of emergency department encounters where antibiotics were prescribed to treat acute otitis media (AOM) are presented here. Information about antimicrobial prescriptions were found in the medical records of children receiving an otoscopic exam by a participating clinician.
Time Frame
Month 6
Secondary Outcome Measure Information:
Title
Number of Diagnoses of Acute Otitis Media (AOM)
Description
The number of emergency department encounters where a diagnosis of acute otitis media (AOM) was made is presented here. Information about the diagnosis of AOM was found in the medical records of children receiving an otoscopic exam by a participating clinician.
Time Frame
Month 6
Title
Number of Diagnoses of Otitis Externa
Description
The number of emergency department encounters where a diagnosis of otitis externa was made is presented here. Information about the diagnosis of otitis externa was found in the medical records of children receiving an otoscopic exam by a participating clinician.
Time Frame
Month 6
Title
Clinician Acceptability of the Smartphone Otoscopic Device
Description
Clinicians randomized to use the smartphone otoscopic device completed a survey to assess the acceptability of this device compared to the historical use of a conventional otoscope. The survey, developed specifically for this study, asked clinicians to report on their preference for using the smartphone otoscope over the conventional otoscope, whether the device increased their ability to diagnose AOM, and the perceived impact on antibiotic prescribing.
Time Frame
Month 6

10. Eligibility

Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Participants must be a pediatric emergency care clinicians providing care at an emergency department a participating children's hospital Willing to agree to random assignment to either a smartphone otoscope device or a conventional otoscope device for the 6-month study period Willing to log patient encounters that included the an otoscopic examination for non-traumatic indication for each shift Willing to document and report episodes of care in which the assigned otoscopic device could not be used on a study-eligible otoscopic examination Willing to complete an end of study assessment, if assigned to use the smartphone otoscope Exclusion Criteria: Declines to give informed consent to participate in the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrea Shane, MD, MPH, MSc
Organizational Affiliation
Emory University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Healthcare of Atlanta at Hughes Spalding
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30303
Country
United States
Facility Name
Children's Healthcare of Atlanta at Egleston
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Pediatric Emergency Department Smartphone Otoscope Study (PED-Oto)

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