Anaesthesia and mHealth
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
This study consists of a simple online survey that takes approximately 3 minutes to complete.
The study aims to assess the confidence of the belgian anaesthesiologists on smartphone applications and dedicated smartphone peripherals, on how these can be used in daily practice, as well as what their wishes for further developments are.
Study Type
Study Type
Enrollment (Anticipated)
Enrollment
Contacts and Locations
Study Contact
Study Contact
- Name: Veerle Van Mossevelde, Data Nurse
- Phone Number: +3224763134
- Email: veerle.vanmossevelde@uzbrussel.be
Study Contact Backup
- Name: Annelies De Cock, MSc
- Phone Number: +3224749906
- Email: annelies.decock@uzbrussel.be
Study Locations
-
-
Brussel
-
Jette, Brussel, Belgium, 1090
- Recruiting
- Universitair Ziekenhuis Brussel
-
Contact:
- Veerle Van Mossevelde, Data Nurse
- Phone Number: +3224763134
- Email: veerle.vanmossevelde@uzbrussel.be
-
Contact:
- Annelies De Cock, MSc
- Phone Number: +3224749906
- Email: annelies.decock@uzbrussel.be
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Active diploma-holding Anesthesiologist working in Belgium
Exclusion Criteria:
- None
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Questionnaire about the Confidence (scale 0-5) on Mobile Apps and Peripheral Devices in Anesthesiology
Time Frame: One single time-point assessment (time of filling in the questionnaire) during 3 months (time during which the filling-in of the questionnaire is possible)
|
Confidence of Anesthesiologist on the use of Mobile Apps and Peripheral Devices in improving anesthesia care.
|
One single time-point assessment (time of filling in the questionnaire) during 3 months (time during which the filling-in of the questionnaire is possible)
|
Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Study Director: Jan Poelaert, MD, PhD, Universitair Ziekenhuis Brussel
- Principal Investigator: Hugo Carvalho, MD, MSc, Universitair Ziekenhuis Brussel
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Anticipated)
Primary Completion
Study Completion (Anticipated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
Other Study ID Numbers
- ANESmHealth
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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.
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