The Effectiveness of Acupressure on Reducing Pain and Improving Gastrointestinal Function After Laparoscopic Surgery

Not Applicable

• Conditions: Postoperative Pain
• Interventions: Behavioral: acupressure; Behavioral: sham acupressure

• Registration Number: NCT05360173
• Lead Sponsor: China Medical University Hospital

Brief Summary

The purpose of the study is to explore the effect if acupressure reducing pain after laparoscopic surgery. The study is designed as an experimental research with repeat measurement design. The patients who are eligible for laparoscopic for general surgery and colorectal surgery in a medical center in the central part of Taiwan. The intervention of the research starts from the first date of postoperative day and the patient has the postoperative pain. The participant will be randomized into experimental group and control group. These two groups will be given true acupressure and sham acupressure twice daily. The participant will be observation the postoperative pain and postoperative recovery.

Detailed Description

Laparoscopic is increasing in this decade. The surgical trauma caused postoperative pain which cannot be avoid. It is the significant challenge and the thorny issue of the healthcare providers, also, be discussed for many decades. Several clinical researches have been verified acupuncture and related method have been as adjuvant efficacy treatment for decreasing postoperative pain. Acupressure is the method of the thumb put acupoint, and therapeutic effectiveness is similar to acupuncture. Acupressure is allowed to a nurse work independently due to noninvasive treatment. However, the less of the clinical studies explore the efficacy of acupressure reducing the postoperative pain after laparoscopic. The result of the research will provide the efficacy of reducing postoperative laparoscopic pain and wish to improve the quality of care.

Study Timeline

• Study First Submitted: 2022-04-21
• Study First Submitted QC: 2022-04-28
• Status Verified: 2022-05
• Study First Posted: 2022-05-04
• Last Update Submitted: 2022-05-04
• Last Update Posted: 2022-05-10
• Study Start: 2022-06-16
• Primary Completion: 2022-12-01
• Study Completion: 2022-12-31

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 86

Inclusion Criteria

• laparoscopic surgery on the organ of liver, gastric, small intestine, colon under general anaethesia
• the American Society of Anesthesiologists (ASA) :I - III
• above 20 years old
• the state of consciousness is alert
• Chinese or Taiwanese speaker

Exclusion Criteria

• surgical procedure: resection, low anterior resection, Roux-en-Y Gastric Bypass and Whipple procedure (pancreaticoduodenectomy)
• postoperative length of hospital stay less than 3 days
• patient have pregnant, maternity, breastfeeding, chronic pain history, coagulation disorder or skin injury on the acupoints.
• drug abuse, alcoholism
• Patient-controlled analgesia

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Experimental group	acupressure	The experimental group not only have the routine treatment, but have acupressure when they back to the ward with the following 3 days . The effectiveness evaluation was carried out by the same researcher before and after intervention. There are three assessments in this study: primary outcome including postoperative pain and bowel movement. The short-form McGill Pain Questionnaire is used to measure the quality of pain, Visual Analog Scale is used to the pain intensity and stethoscope is used to listen to the bowel sound. The study, also, will be recorded postoperative exhaust time, the postoperative date of Indwelling drainage tube and postoperative length of stay.
Control group	sham acupressure	The control group will have the same treatment and the evaluation, except received sham acupoint.

Primary Outcome Measures

Name	Time	Method
medication consumption	3 days	The data is recorded from the patient chart about the drugs consumption after surgery. That is included opioid, non-steroidal anti-Inflammatory drugs, prokinetic agent and anti-flatulence drugs. The more medications are used mean the worse outcome.
Postoperative pain intensity	3 days	Visual Analog Scale (VAS) of pain is used to measure the pain intensity. The scale of 0 = no pain and 10 = the worst pain, is a 10 cm scale marked in cm. The higher scores means the worse outcome.
The quality of postoperative pain	3 days	The short-form McGill Pain Questionnaire (SF-MPQ) is used to measure the quality of pain. The Chinese version is used that consists of 16 descriptors (12 sensory; 4 affective) which rated 0 = none, 1 = mild, 2 = moderate or 3 = severe, and Present Pain Intensity (PPI) and a visual analogue scale (VAS). The higher score means the worse outcome.

Secondary Outcome Measures

Name	Time	Method
postoperative length of stay	Postoperative day to discharge (about 5-7 days)	recording from the chart, time is the shorter the better
Times of exhaust air	3 days	The data is recorded by ask the patient whether they have exhaust air or not after intervention. If the patient has exhaust air after the intervention, means the good outcome.
recovery of bowel movement	3 days	The stethoscope is used to listen to the bowel sound, which will be measured by the researcher. The bowel sound increase means the good outcome.
Timing of first flatus	3 days	asking the patient the timing of the first flatus after surgery, time is the shorter the better