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Acupuncture-like Transcutaneous Electrical Nerve Stimulation on Bowel Symptom and Quality of Life in Patients With Irritable Bowel Syndrome

N

National Taipei University of Nursing and Health Sciences

Status

Terminated

Conditions

Irritable Bowel Syndrome
Acupuncture-like Transcutaneous Electrical Nerve Stimulation

Treatments

Device: acupuncture-like transcutaneous electrical nerve stimulation

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

To discuss the effects of improving the irritable bowel syndrome patients' quality of life and defecation after implementing acupuncture-like Transcutaneous Electrical nerve stimulation.

Full description

This experiment will use a clinical design that will collect cases in a local teaching hospital. The way of convenience sampling will gather from the irritable bowel syndrome patients. After a questionnaire, randomly to make invention and control groups. Invention and control groups are 4 weeks and 3 weeks respectively. Each time will be for 20 minutes acupuncture-like transcutaneous electrical nerve stimulation treatment. The Control group will still have normal nursing. There will be 72 patients in two groups. The measured timing will be in the second, fourth, and eighth weeks after the prediction and invention.

Enrollment

30 patients

Sex

All

Ages

20+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Those who are at least 20 years old (inclusive) and are willing to sign a written informed consent after explaining the purpose of the research.
  2. A patient with irritable bowel syndrome diagnosed by a doctor for at least 6 months (inclusive).
  3. Communicate in Mandarin or Hokkien.

Exclusion criteria

  1. Those who cannot take care of themselves in daily life.
  2. Those who have had severe abdominal and colorectal surgery.
  3. Those who have been diagnosed with inflammatory bowel disease or colorectal cancer.
  4. Those with a history of mental illness, such as schizophrenia and obsessive- compulsive disorder.
  5. Women who are pregnant, breastfeeding, and less than 12 months after delivery.
  6. Other serious diseases, such as acute myocardial infarction, endocrine disease, decompensated cirrhosis, stroke, and end-stage renal disease, etc.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

30 participants in 2 patient groups

acupuncture-like transcutaneous electrical nerve stimulation
Experimental group
Description:
1. The experimental group received acupuncture-like transcutaneous electrical nerve stimulation three times a week for 4 weeks. 2. Invention and control groups are 4 weeks and 3 weeks respectively. Each time will be for 20 minutes acupuncture-like transcutaneous electrical nerve stimulation treatment
Treatment:
Device: acupuncture-like transcutaneous electrical nerve stimulation
Control group:conventional therapy
No Intervention group
Description:
The control group will receive routine care.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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