- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04473495
The Impact of Video Information on Preoperative Anxiety in Interventional Cardiology Patients. (VATIC)
July 15, 2020 updated by: Central Hospital, Nancy, France
This study evaluates the impact of educative videos on anxiety for patients entering hospital for cardiology intervention
Study Overview
Status
Unknown
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
74
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Ugo Righetto
- Phone Number: 0033383153256
- Email: ugo.righetto@gmail.com
Study Contact Backup
- Name: Jean-Marc Sellal
- Phone Number: 0033383153256
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
patient entering hospitalisation in cardiology department for a cardiology intervention
Description
Inclusion Criteria:
- patient entering hospitalisation in cardiology department for a cardiology intervention.
Exclusion Criteria:
- protected person.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
video
patients who enjoyed an educational video
|
educational video before intervention
|
control
patients who didn't enjoy any educational video
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
anxiety
Time Frame: 1 year
|
anxiety measured with STAI Y-A questionnaire
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Jean-Marc Sellal, Central Hospital, Nancy, France
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ANTICIPATED)
August 1, 2020
Primary Completion (ANTICIPATED)
September 1, 2020
Study Completion (ANTICIPATED)
October 1, 2020
Study Registration Dates
First Submitted
May 5, 2020
First Submitted That Met QC Criteria
July 15, 2020
First Posted (ACTUAL)
July 16, 2020
Study Record Updates
Last Update Posted (ACTUAL)
July 16, 2020
Last Update Submitted That Met QC Criteria
July 15, 2020
Last Verified
May 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2019PI013
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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