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

C

CHEN, CHIA-CHEN

Status

Completed

Conditions

Esophageal Cancer
Gastrointestinal Dysfunction

Treatments

Other: acupressure

Study type

Interventional

Funder types

Other

Identifiers

NCT06275165
202301754B0

Details and patient eligibility

About

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.

Full 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.

Enrollment

48 patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

48 participants in 2 patient groups

acupressure
Experimental group
Description:
Participants received routine care and acupressure.
Treatment:
Other: acupressure
no intervision
No Intervention group
Description:
received routine care

Trial contacts and locations

1

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Central trial contact

Chia-Chen Chen

Data sourced from clinicaltrials.gov

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