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

Not Applicable
Completed
Conditions
Nurse's Role
Interventions
Other: preoperative psychological intervention
Registration Number
NCT04918485
Lead Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
Brief 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
162
Inclusion Criteria

the patients who will undergo cholecystectomy surgery

Exclusion Criteria

the patients who can not well communicate

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
the experimental group received psychological interventionpreoperative psychological intervention-
Primary Outcome Measures
NameTimeMethod
The total cooperation ratethrough study completion, an average of half a year

The total cooperation rate was 95.00% in the experimental group and 77.00% in the control group.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

2nd affiliated hospital, school of medicine, Zhejiang University

🇨🇳

Hangzhou, Zhengjiang, China

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