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Preoperative Intervention to Reduce Delirium After Cardiac Surgery

NCT05143580 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2021-12-03

No results posted yet for this study

Summary

This research is designed for experimental quantitative research and is conducted by simple random sampling. Both the control group and the experimental group provided preoperative routine nursing treatment and preoperative medical teaching manuals. The latter adds cognitive therapy and gamification evaluation. Both groups used CAM-ICU to assess the occurrence and duration of postoperative delirium, and DRS-R-98 was used to assess the severity of delirium. After collection, use SPSS 22.0 statistical software package for analysis and processing. The expected result is that the incidence of delirium, the duration of delirium, and the severity of delirium in the experimental group were significantly lower than those in the control group.

Conditions

  • Cardiac Surgery

Interventions

BEHAVIORAL

Cognitive therapy

* The anesthesiologist will provide the patient with instructions for preoperative anesthesia. * The operating room nurses will introduce the operating room environment and surgical care instructions to the patient. * Provide a manual for disease health education. * Provide post-operative care and environmental imaging materials, explain the importance of intensive care unit routines and related equipment, indwelling pipelines, related nursing staff, post-operative care methods, and provide imaging and health education manuals for explanation. * Use gamification to evaluate: pain relief skills, lung expansion skills.

BEHAVIORAL

Routine care

* The anesthesiologist will provide the patient with instructions for preoperative anesthesia. * The operating room nurses will introduce the operating room environment and surgical care instructions to the patient. * Provide a manual for disease health education.

Sponsors & Collaborators

  • Changhua Christian Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-12-01
Primary Completion
2022-10-30
Completion
2022-10-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05143580 on ClinicalTrials.gov