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临床试验/NCT06824857
NCT06824857已完成不适用

Effect of Postoperative Abdominal Massage on Bowel Movements in Patients With Subarachnoid Hemorrhage

Gazi University2 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2024年9月16日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
64
试验地点
2
主要终点
Time To Defecate

研究概览

简要总结

The study will be conducted as a randomized controlled trial to determine the effect of postoperative abdominal massage on bowel movements in patients who underwent surgery after subarachnoid hemorrhage and are hospitalized in the neurosurgery intensive care unit.

详细描述

The study will be conducted as a randomized controlled trial to determine the effect of postoperative abdominal massage on bowel movements in patients who underwent surgery after subarachnoid hemorrhage and are hospitalized in the neurosurgery intensive care unit. The sample of the study will consist of a total of 64 patients, 32 in the experimental group and 32 in the control group, hospitalized in the tertiary neurosurgery intensive care unit. Data collection tools are the "Descriptive Characteristics Form" and the "Patient Follow-up Form".The statistician will determine whether the patients who meet the sampling criteria will be assigned to the experimental or control group through randomization. The stratified randomization method will be used in the study. In this context, patients who meet the inclusion criteria from the start date of the study in the Neurosurgery Intensive Care Unit will be randomized by assigning them to the control group and abdominal massage groups, respectively. Patients will be assigned to the control and abdominal massage groups in this order until the sample size is reached. The CONSORT diagram will be used in the randomization of patients.

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 64 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •• 18 years of age or older
  • •Underwent neurovascular surgery
  • •Received general anesthesia
  • •Have no wounds, surgical intervention, or radiotherapy in the abdominal region
  • •Have no bowel obstruction, irritable bowel syndrome, inflammatory bowel disease, abdominal herniation, or bowel cancer
  • •Began oral feeding at the 6th hour post-surgery
  • •Stayed in the intensive care unit for 3 or more days
  • •Have a Glasgow Coma Scale (GCS) score of 9 or above
  • •Have no signs of acute abdomen
  • •Have no intra-abdominal infection
  • •No mechanical ventilation
  • •Mobilezed in the preoperative period
  • •Unable to mobilize after surgery
  • •Evaluated by the intensive care physician with no contraindications for abdominal massage
  • •Have a first-degree relative who has given consent

排除标准

  • •Patients with the following conditions will be excluded from the sample:
  • •Those with chronic constipation, fecal incontinence, or diarrhea
  • •Those fed with a fiber-enriched nutritional solution (e.g., Nutrison Protein Plus Multifibre®, Fresubin Original Fibre®, Isosource Fiber®, Jevity Plus®)
  • •Those fed via nasogastric enteral tube
  • •Those receiving parenteral nutrition
  • •Patients with a BMI > 40 (morbid obesity)

研究组 & 干预措施

Abdominal Massage Application Group

Experimental

After explaining the purpose of the study to the relatives of patients in the abdominal massage group, the "Introductory Characteristics Form" will be filled out. Abdominal massage will be performed according to the Checklist at the 6th hour after surgery and at the same times in the morning and evening for the first 3 days post-surgery. Before and 15 minutes after the abdominal massage application, bowel sounds will be auscultated, abdominal circumference will be measured with a measuring tape, and abdominal tension will be observed and recorded in the patient follow-up form.

干预措施: Abdominal Massage Application (Other)

Control Group

No Intervention

After explaining the purpose of the study to the relatives of patients in the control group, the "Introductory Characteristics Form" will be filled out. At the same times as the experimental group, bowel sounds will be auscultated in the control group without any intervention, abdominal circumference will be measured with a measuring tape, and abdominal tension will be observed

结局指标

主要结局

Time To Defecate

时间窗: From the 6th hour after surgery until the end of the 3rd day after surgery

Time of first defecation

Bowel Sounds

时间窗: From the 6th hour after surgery until the end of the 3rd day after surgery

Frequency of bowel sounds heard per minute

Abdominal Distension

时间窗: From the 6th hour after surgery until the end of the 3rd day after surgery

To be assessed by measuring the abdominal circumference with a tape measure

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Zühal Erdoğan

RN, PhD, Assistant Professor

Gazi University

研究点 (2)

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