The Effect Of Acupressure Applıcatıon On Postoperative Pain Level İn Women With Abdominal Gynecologıcal Surgery: Randomized Controlled Study
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 102
- 试验地点
- 2
- 主要终点
- postoperative pain level
研究概览
简要总结
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.
详细描述
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •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
排除标准
- •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
结局指标
主要结局
postoperative pain level
时间窗: 7 month
Pain will be measured with the Short-Form McGill pain questionnaire (SF-MPQ) before and after the application
次要结局
未报告次要终点
研究者
Meliha Dönmez
master student
Saglik Bilimleri Universitesi