Viewing Study NCT06275165



Ignite Creation Date: 2024-05-06 @ 8:10 PM
Last Modification Date: 2024-10-26 @ 3:21 PM
Study NCT ID: NCT06275165
Status: RECRUITING
Last Update Posted: 2024-03-29
First Post: 2024-02-17

Brief Title: The Effects of Acupressure on Improving Postoperative Gastrointestinal Symptom Distress in Esophageal Cancer Patients
Sponsor: CHEN CHIA-CHEN
Organization: Chang Gung Memorial Hospital

Study Overview

Official Title: The Effects of Acupressure on Improving Postoperative Gastrointestinal Symptom Distress in Esophageal Cancer Patients
Status: RECRUITING
Status Verified Date: 2024-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study is a quasi-experimental design clinical trial with the primary objective of comparing the health status of patients with esophageal cancer Participants were divided into an experimental group and a control group Patients in the experimental group received routine care and acupressure for 5 consecutive days starting from the day after entering the ward after esophageal cancer surgery in the control group participants received routine care and Participants were assessed on the Gastrointestinal Symptom Distress Scale at the end of the intervention The aim of this study was to verify the effectiveness of acupressure in improving of gastrointestinal symptoms distress after esophageal cancer surgery
Detailed Description: Esophageal cancer is one of the common and highly fatal malignant tumors and its incidence rate is increasing every year and most of them are in the middle and advanced stages when diagnosed Surgery is the standard treatment for the eradication of esophageal cancer which can effectively reduce the mortality rate and improve the survival rate but the patients often experience gastrointestinal discomfort after surgery which impedes the intake of nutrients and the bodys recovery The purpose of this study was to investigate the effectiveness of acupressure in improving the postoperative gastrointestinal discomfort in patients with esophageal cancer An experimental study design was adopted and patients were assigned to the experimental group and the control group in a time-divided manner The experimental group was assigned to the experimental group and the control group in a time-separated manner The experimental group received regular care from the first day to the fifth day after the patients were transferred from the intensive care unit to the hospital ward after the surgery and they received acupressure at the Neiguan point of the upper limbs and the four acupoints of the foot Sanli of the lower limbs twice a day for 3 minutes each for a total of 12 minutes while the control group received regular care in the first day of the study In this study the gastrointestinal symptoms of the experimental group before and after acupressure were collected and compared with those of the control group in order to verify the effectiveness of acupressure in improving gastrointestinal symptoms during postoperative nutritional support for jejunostomy

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None