A Survey of Google Glass by Orthopaedic Trauma Patients and Surgeons
GoogleGlass
A Survey-driven Evaluation of Patients Response to the Introduction of Google Glass in the Orthopaedic Trauma Clinic
2 other identifiers
interventional
127
1 country
1
Brief Summary
Patients seen in the Orthopaedic Trauma clinic will be asked to consent for potential video/picture recording using the Google Glass device during their visit with the orthopaedic surgeon or resident. The investigators want to record the patient's level of acceptance and response to this new technology. There are two arms: Patients seen by a doctor wearing the Google Glass device and those that will not be exposed. Both groups will be asked to complete a survey after their clinic visit. The device users (doctor) will complete a survey which will evaluate how effective this new tool is in the Orthopaedic clinical setting.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Aug 2014
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 24, 2014
CompletedStudy Start
First participant enrolled
August 1, 2014
CompletedFirst Posted
Study publicly available on registry
August 20, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 30, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2018
CompletedMay 15, 2020
May 1, 2020
3.8 years
July 24, 2014
May 13, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Patient Evaluation Survey
Day one
Secondary Outcomes (1)
Surgeon Evaluation Survey
Day one
Study Arms (2)
Google Glass
OTHERInvestigators using Google Glass during clinic visit
No Google Glass
NO INTERVENTIONInvestigator will not be using Google Glass during clinic visit
Interventions
The device is a wearable, voice-controlled Android device that resembles a pair of eyeglasses and displays information directly in the user's field of vision
Eligibility Criteria
You may qualify if:
- All patients seen in the Montreal general Hospital (MGH) - Orthopaedic Trauma Clinic and capable of reading French or English.
You may not qualify if:
- All patients that have cognitive impairment or language difficulties that would impede completion of the survey will be excluded from the study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Montreal General Hospital
Montreal, Quebec, H3G 1A4, Canada
MeSH Terms
Conditions
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Edward J Harvey, MDCM FRCSC
RI-MUHC
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- MDCM FRCSC
Study Record Dates
First Submitted
July 24, 2014
First Posted
August 20, 2014
Study Start
August 1, 2014
Primary Completion
May 30, 2018
Study Completion
July 1, 2018
Last Updated
May 15, 2020
Record last verified: 2020-05
Data Sharing
- IPD Sharing
- Will not share