Effects of Providing Preprint Preoperative Anesthetic Risk Information

Phase 1

Completed

• Conditions: Preoperative Anxiety
• Interventions: Other: preprint preoperative anesthetic risk information

• Registration Number: NCT00816699
• Lead Sponsor: Mahidol University

Brief Summary

Proportion of patients in study group(preprint preoperative anesthetic risk should have more anxiety, more knowledge, and more cancellation than controlled group

Detailed Description

Not available

Study Timeline

• Study Start: 2008-12
• Study First Submitted: 2009-01-01
• Study First Submitted QC: 2009-01-02
• Study First Posted: 2009-01-05
• Primary Completion: 2010-08
• Study Completion: 2010-09
• Status Verified: 2011-03
• Last Update Submitted: 2011-03-10
• Last Update Posted: 2011-03-11

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 103

Inclusion Criteria

• Inpatients scheduled for surgery under general anesthesia with or without regional anesthesia
• Low to moderate risk surgery

Exclusion Criteria

• Patient's refusal
• Patients scheduled for cardiovascular surgery and neurosurgery
• Patients with consciousness change following surgery
• Emergency case
• CNS or psychological diseases

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
2	preprint preoperative anesthetic risk information	Preprint preoperative risk information
1	preprint preoperative anesthetic risk information	Routine anesthetic risk information

Primary Outcome Measures

Name	Time	Method
Spielberger State Trait Anxiety Inventory Scale	5 days

Secondary Outcome Measures

Name	Time	Method
Knowledge, proportion of patients who cancel surgery, proportion who refuse regional anesthesia	5 days

Trial Locations

Locations (1)

Faculty of Medicine, Siriraj Hospital, Mahidol Unversity; 🇹🇭 Bangkok, Thailand