VATIC: The Impact of Video Information on Preoperative Anxiety in Interventional Cardiology Patients.
Sponsor
Central Hospital, Nancy, France (Other)
Overall Status
Unknown status
CT.gov ID
NCT04473495
Collaborator
(none)
74
2
Study Details
Study Description
Brief Summary
This study evaluates the impact of educative videos on anxiety for patients entering hospital for cardiology intervention
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Study Design
Study Type:
Observational
Anticipated Enrollment
:
74 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
The Impact of Video Information on Preoperative Anxiety in Interventional Cardiology Patients.
Anticipated Study Start Date
:
Aug 1, 2020
Anticipated Primary Completion Date
:
Sep 1, 2020
Anticipated Study Completion Date
:
Oct 1, 2020
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
video patients who enjoyed an educational video |
Device: educational video
educational video before intervention
|
control patients who didn't enjoy any educational video |
Outcome Measures
Primary Outcome Measures
- anxiety [1 year]
anxiety measured with STAI Y-A questionnaire
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
- patient entering hospitalisation in cardiology department for a cardiology intervention.
Exclusion Criteria:
- protected person.
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- Central Hospital, Nancy, France
Investigators
- Principal Investigator: Jean-Marc Sellal, Central Hospital, Nancy, France
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Central Hospital, Nancy, France
ClinicalTrials.gov Identifier:
NCT04473495
Other Study ID Numbers:
- 2019PI013
First Posted:
Jul 16, 2020
Last Update Posted:
Jul 16, 2020
Last Verified:
May 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms: