BATHE Method on Preoperative Anxiety, Patient Satisfaction and Individual Anesthesia Concerns

Not Applicable

Completed

• Conditions: Patient Satisfaction; Anesthesia; Reaction; Anxiety Preoperative

• Registration Number: NCT04386486
• Lead Sponsor: Cumhuriyet University Hospital

Brief Summary

In this study the goal is to determine the causes of concern among the patients who will undergo surgical operations and receive general anesthesia, to gauge their preoperative anxiety levels and to study the effects of the BATHE method on preoperative anxiety and patient satisfaction.

Detailed Description

In this study the goal is to determine the causes of concern among the patients who will undergo surgical operations and receive general anesthesia, to gauge their preoperative anxiety levels and to study the effects of the BATHE method on preoperative anxiety and patient satisfaction.

500 patients who were planned to undergo elective surgery and under general anesthesia as anesthesia method were included in the study. Demographic data of patients, their three biggest fears of anesthesia and APAIS scores were recorded. The patients were divided into two groups, they underwent BATHE anamnesis or standard anamnesis methods according to their groups, then their APAIS and patient satisfaction scores were recorded.

Study Timeline

• Study Start: 2017-12-13
• Primary Completion: 2018-12-30
• Study Completion: 2019-02-10
• Status Verified: 2020-05
• Study First Submitted: 2020-05-09
• Study First Submitted QC: 2020-05-09
• Last Update Submitted: 2020-05-09
• Study First Posted: 2020-05-13
• Last Update Posted: 2020-05-13

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 500

Inclusion Criteria

A) ASA I-II patients

Exclusion Criteria

A) ASA III-IV B) illiterate patients C) patients with known psychiatric disorders D) patients with chronic sedative E) antipsychotic drug use F) patients with a history of going to psychiatry in the last year G) patients with any cancer diagnosis were not included in the study.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
t-test	0-30 minutes	when measurements taken from two independent groups are compared, the independent T-test was used.

Trial Locations

Locations (1)

Cemil Ahmet Isbir; 🇹🇷 Sivas, Turkey