The Effects of Acupressure on Improving Postoperative Gastrointestinal Symptom Distress in Esophageal Cancer Patients

NCT ID: NCT06275165

Last Updated: 2025-08-07

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 48 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-03-27
• Study Completion Date: 2025-07-18

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 body's 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.

Conditions

Esophageal Cancer; Gastrointestinal Dysfunction

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: SINGLE

Study Groups

acupressure

Participants received routine care and acupressure.

Group Type: EXPERIMENTAL

acupressure

Intervention Type: OTHER

In the experimental group, routine nursing care and acupressure (Neiguan and Zusanli points) were performed from the 1st to the 5th day after the postoperative transfer from the ward to the hospital room. Twice a day, 3 minutes each time, 12 minutes in total.

no intervision

received routine care

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

acupressure

In the experimental group, routine nursing care and acupressure (Neiguan and Zusanli points) were performed from the 1st to the 5th day after the postoperative transfer from the ward to the hospital room. Twice a day, 3 minutes each time, 12 minutes in total.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Hospitalized men and women who agree to participate in this study
• Patients diagnosed with esophageal cancer based on pathological tissue section results
• Nutritional support through jejunostomy in post esophagectomy patients
• A sufficient level of education to understand study procedures and be able to communicate with site personnel

Exclusion Criteria

• Pregnant or lactating women
• Diagnosed and treated for peripheral vascular disease within 3 months prior to surgery.
• Those with unstable vital signs and septicemia infection after surgery.
• Those who are suffering from blood diseases with abnormal coagulation function, or Currently taking anticoagulant drugs.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

CHEN, CHIA-CHEN

OTHER

Sponsor Role: lead

Responsible Party

CHEN, CHIA-CHEN

Principal Investigator

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Chia-Chen Chen

Role: PRINCIPAL_INVESTIGATOR

Chang Gung Memorail Hospital

Locations

Chang Gung Memotial Hospital

Taoyuan District, , Taiwan

Countries

Taiwan

Other Identifiers

202301754B0

Identifier Type: -

Identifier Source: org_study_id