Effect of Acupressure on Postoperative Pain With Gynecologıcal Surgery

Saglik Bilimleri Universitesi

Status: Completed

Conditions: Acupressure; Nurse's Role; Post Operative Pain

Treatments: Other: acupressure

Study type: Interventional

Funder types: Other

Identifiers

NCT06172439

SBU-MDONMEZ-001

Details and patient eligibility

About

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.

Full 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.

Enrollment: 102 patients

Sex: Female

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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102 participants in 2 patient groups

experimental group

Experimental group

Description:

Women in the intervention group will receive acupressure for 12 minutes.

Treatment:

Other: acupressure

control group

No Intervention group

Description:

Women in the control group will not receive acupressure and will continue with routine care.