Early COVID 19 pneumonia Infections and Infestations
Conditions
Interventions
After informed consent, participants will complete an electronic demographic survey and receive a package containing a disinfected hand-held high-frequency linear ultrasound probe (Philips Lumify, Phi
1—Very Hard, 2—Hard, 3—Neutral, 4—Easy, 5—Very Easy.
An a-priori planned independent review will be undertaken by three outside lung ultrasound experts, who will rate both the image qu
Sponsors
University of Calgary
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Adults self-isolating according to public health measures for the purpose of reducing person to person transmission of COVID 19
Exclusion criteria
Exclusion criteria: 1. Non-English speaking 2. Illiterate 3. Not willing to participate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Acquisition of good-quality interpretable images based on the 14-zone method proposed by Soldati for International Standardization of the Use of Lung Ultrasound for Patients with COVID-19 as assessed by the lung ultrasound expert during telementored self-performed lung ultrasound | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. The ability for volunteers to physically reach each anatomic location of a standard recommended COVID lung ultrasound examination as assessed by the lung ultrasound expert during telementored self-performed lung ultrasound 2. Calculated test performance characteristics of standard lung examination protocols recommending a variety of differing anatomic assessment locations measured using the Likert scale generated by the lung ultrasound experts reviewing the telementored self-performed lung ultrasound, and patient self-rated user difficulty scores of a different Likert scale following the examination | — |
Countries
Canada
Outcome results
None listed