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NCT04918485 Clinical Trial

Effect of Preoperative Psychological Intervention on the Degree of Cooperation During Tracheal Catheter Extubation in Patients

Nurse's Role Clinical Trial

Official title:
Effect of Preoperative Psychological Intervention on the Degree of Cooperation During Tracheal Catheter Extubation in Patients Under General Anesthesia During Awakening Period

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04918485
Other study ID # SAHZhejiangUChenshuyi
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2020
Est. completion date December 31, 2020

Study information
Verified date January 2021
Source Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The patients in the experimental group received the relevant knowledge education in the recovery period 30 minutes before anesthesia. The operation time, anesthesia time, cooperation degree score, total cooperation rate and patient satisfaction were observed and recorded. Results: there was no significant difference in operation time and anesthesia time between the experimental group and the control group (P < 0.05). The percentage of patients in the experimental group was 20.12% and 70.89% respectively, while that in the control group was 40.32% and 20.73% respectively (P < 0.05). The total cooperation rate was 95.00% in the experimental group and 77.00% in the control group. There was significant difference between the two groups (P < 0.05). The satisfaction of patients in the experimental group was 95%. 65% of the patients in the control group were satisfied (P < 0.05). Conclusion: preoperative psychological intervention for patients with general anesthesia and endotracheal intubation can significantly reduce the restlessness and uncooperative phenomenon during extubation, and improve the cooperation rate and satisfaction of patients.

Recruitment information / eligibility
Status Completed
Enrollment 162
Est. completion date December 31, 2020
Est. primary completion date December 2, 2020
Accepts healthy volunteers No
Gender All
Age group 12 Years to 80 Years
Eligibility Inclusion Criteria: the patients who will undergo cholecystectomy surgery Exclusion Criteria: the patients who can not well communicate

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• preoperative psychological intervention
including closing the relationship between nurse and patient , knowledge education,

Locations
Country Name City State
China 2nd affiliated hospital, school of medicine, Zhejiang University Hangzhou Zhengjiang

Sponsors (1)
Lead Sponsor Collaborator
Second Affiliated Hospital, School of Medicine, Zhejiang University

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary The total cooperation rate The total cooperation rate was 95.00% in the experimental group and 77.00% in the control group. through study completion, an average of half a year
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