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
  • Device: educational video

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

  1. 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:

Study Results

No Results Posted as of Jul 16, 2020