Effect of Acupressure on Postoperative Pain With Gynecologıcal Surgery

Not Applicable

Completed

• Conditions: Post Operative Pain; Acupressure; Nurse's Role
• Interventions: Other: acupressure

• Registration Number: NCT06172439
• Lead Sponsor: Saglik Bilimleri Universitesi

Brief Summary

In this study, the effect of acupressure on postoperative pain level in women with abdominal gynecologıcal surgery will be studied and it will be conducted as a randomized controlled intervention study to examine the relationships with each other.The sample group will consist of 102 women, 51 in the intervention group and 51 in the control group.Within the scope of the study, the data will be collected using the 'Personal Information Form and Short-Form McGill Pain Questionnaire (SF-MPQ)' created by the researcher. Data will be analyzed using SPSS-26 package.

Detailed Description

In this study, the effect of acupressure on postoperative pain level in women with abdominal gynecologıcal surgery will be studied and it will be conducted as a randomized controlled intervention study to examine the relationships with each other.The sample group will consist of 102 women, 51 in the intervention group and 51 in the control group.Within the scope of the study, the data will be collected using the 'Personal Information Form and Short-Form McGill Pain Questionnaire(SF-MPQ)' created by the researcher. Data will be obtained by the researcher by faceto-face interviews with women. In addition, women in the intervention group will receive acupressure once on postoperative days 0 and 1. Acupressure points related to gynecological surgery (large intestine (LI4), stomach (ST36) and spleen (SP6)) will be applied for a total of 12 minutes with 2 minutes of pressure on each point. Women in the control group will continue their routine care. Data will be evaluated with SPSS-26 package.

Study Timeline

• Study Start: 2023-06-01
• Study First Submitted: 2023-12-07
• Study First Submitted QC: 2023-12-07
• Study First Posted: 2023-12-15
• Primary Completion: 2023-12-30
• Study Completion: 2024-01-30
• Status Verified: 2024-06
• Last Update Submitted: 2024-06-25
• Last Update Posted: 2024-06-26

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 102

Inclusion Criteria

• 20 years of age or older,
• Being literate,
• To be able to understand and speak Turkish,
• No deformity or lesion in the areas where acupressure will be applied,
• Undergoing abdominal gynecologic surgery with general anesthesia,
• Any narcotic or epidural for pain control after surgery lack of analgesia
• Participation in the routine pain protocol of the clinic

Exclusion Criteria

• The presence of any systemic disease that causes chronic pain,
• Receiving spinal or epidural anesthesia,
• Patients who are administered narcotic or any analgesic drug other than the routine pain protocol applied in the clinic after surgery

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
experimental group	acupressure	Women in the intervention group will receive acupressure for 12 minutes.

Primary Outcome Measures

Name	Time	Method
postoperative pain level	7 month	Pain will be measured with the Short-Form McGill pain questionnaire (SF-MPQ) before and after the application

Trial Locations

Locations (1)

Faculty of nursing; 🇹🇷 Ankara, Turkey