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

NCT ID: NCT05042661

Last Updated: 2026-01-06

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-02-01
• Study Completion Date: 2023-02-13

Brief Summary

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

Detailed 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.

Conditions

Acupuncture-like Transcutaneous Electrical Nerve Stimulation; Irritable Bowel Syndrome

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

acupuncture-like transcutaneous electrical nerve stimulation

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

Group Type: EXPERIMENTAL

acupuncture-like transcutaneous electrical nerve stimulation

Intervention Type: DEVICE

The intervention group performed Al-TENS therapy 3 times a week for at least 20 minutes each time for 4 consecutive weeks. The second, fourth, and eighth week after the intervention.

Control group:conventional therapy

The control group will receive routine care.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

acupuncture-like transcutaneous electrical nerve stimulation

The intervention group performed Al-TENS therapy 3 times a week for at least 20 minutes each time for 4 consecutive weeks. The second, fourth, and eighth week after the intervention.

Intervention Type: DEVICE

Eligibility Criteria

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.

• Minimum Eligible Age: 20 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

National Taipei University of Nursing and Health Sciences

OTHER

Sponsor Role: lead

Responsible Party

Tsu Ying Fang

Principal investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Tsu Ying Fang

New Taipei City, , Taiwan

Countries

Taiwan

Other Identifiers

TFang

Identifier Type: -

Identifier Source: org_study_id