- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02788422
Video Discharge Instructions for Acute Otitis Media
The Effectiveness of Video Discharge Instructions for Acute Otitis Media on Knowledge Acquisition and Clinical Outcomes: a Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Providing patients with understandable, comprehensive discharge instructions improves compliance, thereby reducing symptoms and the functional impact of illness. Comprehensive discharge instructions also reduce patient anxiety and increases satisfaction. Unfortunately, in a busy emergency department (ED), discharge instructions are often incomplete. Furthermore, even when discharge instructions have been provided, patients often have difficulty comprehending and/or recalling them. Inadequate discharge instructions are linked to medication errors, suboptimal care post-discharge, and unnecessary return visits to the ED. Patient dissatisfaction with discharge instructions and anxiety have also been linked to poor medication compliance, and an increase in return visits.
Studies have demonstrated that knowledge of pediatric medical conditions can be enhanced through the use of video technology. Specifically, it has been shown that when video discharge instructions are used in place of, or to complement written discharge instructions, patients have a better understanding of their illness and report higher rates of satisfaction. However, no studies to date have explored if clinically relevant outcomes such as symptomatology, function and recidivism can be improved.
This study will examine the utility of video discharge instructions for the diagnosis of acute otitis media (AOM), a leading cause of health care visits among children. AOM affects up to 75% of children before school-age and is the most common illness for which antibiotics are prescribed to children in the United States. In Canada, AOM is associated with substantial use of health services (3.1 hours in an emergency department and 1.8 hours in an outpatient clinic on average per visit) and significantly burdens caregivers in the form of time spent on medical consultations, and time taken off from work. An American study estimated that the cost of one episode of AOM in a 3-month period following diagnosis was $1330.58, with the majority of that cost stemming from the indirect costs of illness, 90% of which was accrued primarily by parental time off work. In Quebec, the total annual cost to the health care system for otitis media and placement of tympanostomy tubes is more than $10 million dollars.
Pain is often substantial in the early course of AOM. Poorly controlled pain is associated with suffering and can be emotionally traumatic, causing anxiety for patients and their caregivers. Efficacious treatment for child pain is paramount in preventing protracted sensitivity to pain. Despite the magnitude of effects that acute pain can have on a child, it is often inadequately assessed and treated. In children less than two years of age, 30% of children continue to experience pain, fever, or both for up to 7 into the illness, thus highlighting the importance of caregiver education on symptom management.
Recurrent AOM is common, 5-15% of children under the age of 2 experience four or more episodes per year. Caregivers of children with recurrent AOM not only judge their child's quality of life markedly lower than caregivers of children of a general population, but also lower than those of children with mild-to-moderately severe chronic conditions. Although uncommon, AOM also has the potential to cause serious complications such as, mastoiditis and bacterial meningitis, if not treated and monitored appropriately.
The investigators hypothesize that video discharge instructions directed at caregivers of children with AOM will be associated with improved symptomatology and functional outcomes, along with improved caregiver knowledge, satisfaction, and anxiety compared to the standard of care, paper-based discharge instructions.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Ontario
-
London, Ontario, Canada
- London Health Sciences Centre
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- All primary caregivers of children aged 6 months to 17 years presenting to the Emergency Department of the Children's Hospital, London Health Sciences Centre, London, Ontario
- Clinical diagnosis of AOM in the context of an upper respiratory tract infection as determined by the treating emergency physician (staff physician or fellow). The treating physician will be asked to rate, using a 10 mm visual analog scale, the likelihood that the patient has AOM using previously published diagnostic criteria. - Physician reports being at least 50% certain, on a visual analog scale in the diagnosis of AOM.
Exclusion Criteria:
- Caregivers whose children have other diagnoses (pneumonia, urinary tract infection, gastroenteritis, or any other condition requiring antibiotics or admission to hospital)
- Previous diagnosis of AOM within 7 days
- Tympanostomy tubes
- Acute tympanic membrane perforation
- Attending caregiver who is not the primary care provider
- Poor English fluency
- Lack of at least a grade 8 literacy level
- No Internet access
- No telephone access for 72 hours following discharge
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Video
Video discharge instructions developed using Easy Sketch Pro3TM software (Easy Sketch Pro, United Kingdom).
It was created by the primary and co-investigator based results on a focus group consisting of two paediatric residents, two paediatric emergency medicine fellows, a paediatric emergency medicine nurse, and a paediatric emergency medicine staff physician.
|
Online video containing information on how to manage symptoms of acute otitis media and when to return to a health care professional.
|
|
Active Comparator: Standard of care
This is a one-page paper handout created by the primary and co-investigator based results on a focus group consisting of two paediatric residents, two paediatric emergency medicine fellows, a paediatric emergency medicine nurse, and a paediatric emergency medicine staff physician.
|
One page paper handout containing information on how to manage symptoms of acute otitis media and when to return to a health care professional.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Daily self-reported Acute Otitis Media Symptom Severity Score
Time Frame: 72 hours
|
At 72 hours
|
72 hours
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-report State Trait Anxiety Inventory at discharge
Time Frame: 72 hours
|
72 hours
|
|
|
Caregiver Satisfaction at 72 hours
Time Frame: 72 hours
|
72 hours
|
|
|
Self-reported number of days of school/work/daycare missed at 72 hours
Time Frame: 72 hours
|
72 hours
|
|
|
Self-reported medication administered daily for 72 hours
Time Frame: 72 hours
|
Number of doses and type of medication administered based on self-report
|
72 hours
|
|
Self-reported return visits to a health care provider at 72 hours
Time Frame: 72 hours
|
Number of visits and type of health care provider and reason based on self-report
|
72 hours
|
|
Number of times online video was viewed in 72 hours
Time Frame: 72 hours
|
72 hours
|
|
|
Change in knowledge score on novel questionnaire before and after intervention in ED
Time Frame: 30 minutes
|
Difference in knowledge questionnaire scores before and immediately following intervention
|
30 minutes
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Naveen Poonai, MD, London Health Sciences Centre
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 10012437
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Otitis Media
-
ClinQure, Inc.NousQ Pte LtdNot yet recruitingOtitis Media | Otitis Media Recurrent | Otitis Media Chronic | Otitis Media in Children | Otitis Media Effusion
-
Vastra Gotaland RegionLund University; Göteborg University; Umeå University; Linkoeping UniversityNot yet recruitingOtitis Media Acute | Otitis Media Effusion
-
Bezmialem Vakif UniversityCompleted
-
Alcon ResearchCompletedOtitis Media With Effusion in Children | Otitis Media Recurrent
-
David Chi, MDActive, not recruitingRecurrent Acute Otitis Media | Chronic Otitis Media With Effusion | Otitis Media in ChildrenUnited States
-
Medical College of WisconsinNational Institutes of Health (NIH); National Institute on Deafness and Other... and other collaboratorsRecruitingOtitis Media | Otitis Media With Effusion | Otitis Media AcuteUnited States
-
Indonesia UniversityCompleted
-
Assistance Publique - Hôpitaux de ParisMinistry of Health, FranceCompletedChronic Serous Otitis Media, Simple or UnspecifiedFrance
-
Stanford UniversityNational Institute on Deafness and Other Communication Disorders (NIDCD)Not yet recruiting
-
Integra LifeSciences CorporationAcclarentCompletedOtitis Media With EffusionUnited States
Clinical Trials on Video discharge instructions
-
Augusta UniversityCompletedEvaluation of Video Discharge Instructions in Improving UnderstandingUnited States
-
Bartın UnıversityCompletedFever | Child, OnlyTurkey
-
Hospital General Universitario Gregorio MarañonCompletedAcute GastroenteritisSpain
-
George Washington UniversityCompletedUrinary Tract Infection | Head Injury | LacerationUnited States
-
Sunnybrook Health Sciences CentreCompletedEmergency Department Discharge Instructions | Instruction Videos
-
Case Comprehensive Cancer CenterTerminatedSurgery | Linear ClosureUnited States
-
NYU Langone HealthCompletedHospital Discharge Summary UnderstandingUnited States
-
Mount Sinai Hospital, CanadaCompleted
-
Hasan Kalyoncu UniversityTerminatedCoronary Artery Disease (CAD) | Coronary Artery Bypass Graft Surgery (CABG) | Postoperative Discharge EducationTurkey (Türkiye)
-
St. Luke's Hospital, PennsylvaniaUnknownAsymptomatic Bacteriuria in Pregnancy