the Effect of Preoperative Pain Education by Anesthesia Nurses on Postoperative Pain Among Adult Patients Undergoing Abdominal Surgery

April 14, 2024 updated by: Hao Li, Chinese PLA General Hospital
To explore the effects of preoperative pain education on postoperative pain among patients undergoing abdominal surgery.

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Estimated)

116

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

Adult patients undergoing Abdominal Surgery

Description

Inclusion Criteria:

  1. voluntary informed consent;
  2. age older than 18 years
  3. abdominal surgery under elective general anesthesia

Exclusion Criteria:

  1. Patients taking long-term analgesics (including opioids, non-steroids, etc.)
  2. Patients with preoperative chronic pain
  3. Have participated in clinical studies in other projects within 3 months prior to signing the informed consent form
  4. subjects not considered by the investigator
  5. subjects refused to participate in the study

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Intervention group
Anesthesia nurses carried out pain-related knowledge education.
Behavioral: education on pain and related knowledge
Before surgery, pain related knowledge was educated.
Other Names:
  • pain-related knowledge education
Blank group
Patients who did not receive any knowledge education.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Occurrence of pain
Time Frame: The first day to the fifth day after surgery.
The NRS scale was used to evaluate the scores.
The first day to the fifth day after surgery.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mastery of the use of patient-controlled analgesia pump
Time Frame: Day 2 after surgery
A series of questions were used to assess patients' mastery of patient-controlled analgesia pump use.
Day 2 after surgery

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Patient satisfaction with postoperative analgesia
Time Frame: Day 5 after surgery
Patient satisfaction with postoperative analgesia
Day 5 after surgery
Adverse events of patients using analgesic pump were recorded
Time Frame: The first day to the fifth day after surgery.
Nausea and vomiting, itching, drowsiness, dizziness
The first day to the fifth day after surgery.
The number of times that the analgesic pump was pressed during each 24h and the amount of analgesic pump remaining at this time were recorded
Time Frame: The first to three days after surgery
The number of times that the analgesic pump was pressed during each 24h and the amount of analgesic pump remaining at this time were recorded
The first to three days after surgery
The use of rescue analgesics after surgery
Time Frame: The first day to the fifth day after surgery.
Temporary painkillers used in the ward
The first day to the fifth day after surgery.
The postoperative sleep status of patients was evaluated
Time Frame: The first day to the fifth day after surgery.
The Richards-Campbell Sleep Questionaire Scale was used
The first day to the fifth day after surgery.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Chinese PLA General Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

April 20, 2024

Primary Completion (Estimated)

January 1, 2025

Study Completion (Estimated)

April 4, 2025

Study Registration Dates

First Submitted

March 17, 2024

First Submitted That Met QC Criteria

March 18, 2024

First Posted (Actual)

March 25, 2024

Study Record Updates

Last Update Posted (Actual)

April 16, 2024

Last Update Submitted That Met QC Criteria

April 14, 2024

Last Verified

April 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • ChinaPLAGHPAIN

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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