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

NCT04918485 | Completed

• 1 other identifier: SAHZhejiangUChenshuyi
• Study Type: interventional
• Target: 162
• Locations: 1 country
• Sites: 1

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.

Conditions

Nurse's Role

Outcome Measures

Primary Outcomes (1)

• 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

Study Arms (2)

the experimental group received psychological intervention

EXPERIMENTAL

Other: preoperative psychological intervention

the control group receive normal process before surgery

NO INTERVENTION

Interventions

preoperative psychological intervention OTHER

including closing the relationship between nurse and patient , knowledge education,

the experimental group received psychological intervention

Eligibility Criteria

• Age: 12 Years - 80 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

• the patients who will undergo cholecystectomy surgery

You may not qualify if:

• the patients who can not well communicate

Sponsors & Collaborators

• Second Affiliated Hospital, School of Medicine, Zhejiang University: lead

Study Sites (1)

2nd affiliated hospital, school of medicine, Zhejiang University

Hangzhou, Zhengjiang, 310000, China

Location

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: PARTICIPANT
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: June 2, 2021
• First Posted: June 8, 2021
• Study Start: September 1, 2020
• Primary Completion: December 2, 2020
• Study Completion: December 31, 2020
• Last Updated: June 8, 2021

Record last verified: 2021-01

Locations

CN (1)