Preoperative Anxiety Evaluation: a New Visual Smileys Scale
Sponsor
Cedars-Sinai Medical Center (Other)
Overall Status
Completed
CT.gov ID
NCT02667847
Collaborator
(none)
200
1
14
14.3
Study Details
Study Description
Brief Summary
Preoperative anxiety is a complex clinical concept with both physiological and psychological consequences.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Detailed Description
This study looks at the need for a more user friendly, rapid tool for measuring preoperative anxiety, specifically by evaluating the visual smileys scale.
Study Design
Study Type:
Observational
Actual Enrollment
:
200 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Preoperative Anxiety Evaluation: a New Visual Smileys Scale
Study Start Date
:
Dec 1, 2012
Actual Primary Completion Date
:
Dec 1, 2013
Actual Study Completion Date
:
Feb 1, 2014
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
Preoperative patients Preoperative patients were asked to verbally rate their anxiety 1=on a scale from 0-10 and 2=using the new smiley scale |
Outcome Measures
Primary Outcome Measures
- Anxiety level, as measured by verbal rating scale or visual smileys scale [up to 5 minutes]
in preoperative setting
Secondary Outcome Measures
- scale preference [up to 5 minutes]
in preoperative setting, comparing verbal rating scale and visual smileys scale
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
-
18 to 80 years old
-
undergoing surgery at Cedars Sinai Medical Center
Exclusion Criteria:
- did not receive sedative or narcotic prior to the interview
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Cedars-Sinai Medical Center | Los Angeles | California | United States | 90048 |
Sponsors and Collaborators
- Cedars-Sinai Medical Center
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Roya Yumul, M.D.,PhD.,
Corresponding Author,
Cedars-Sinai Medical Center
ClinicalTrials.gov Identifier:
NCT02667847
Other Study ID Numbers:
- Pro00030220
First Posted:
Jan 29, 2016
Last Update Posted:
Feb 3, 2016
Last Verified:
Feb 1, 2016
Keywords provided by Roya Yumul, M.D.,PhD.,
Corresponding Author,
Cedars-Sinai Medical Center
Additional relevant MeSH terms: