Effect of Self- Administered Acupressure on Diarrhea Predominant Irritable Bowel Syndrome Patients' Health Outcomes: a Double Blind- Sham Controlled Randomized Clinical Trial

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Record identity and dates

Source

ClinicalTrials.gov

Source record ID

NCT05702255

Title field or adapter rule

{'original_value': "Effect of Self- Administered Acupressure on Diarrhea Predominant Irritable Bowel Syndrome Patients' Health Outcomes: a Double Blind- Sham Controlled Randomized Clinical Trial", 'source_field': 'protocolSection.identificationModule.officialTitle'}

Ingested At

2026-10-31T23:27:35.745344+00:00

Published At

2024-04-30T00:00:00+00:00

Record Updated At

2024-04-30

Source Retrieved At

2026-10-31T22:18:52.668840+00:00

Timestamp Basis

ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter

Date limitation

ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions

["Irritable Bowel Syndrome With Diarrhea"]

protocolSection.statusModule.lastUpdatePostDateStruct

{"date": "2024-04-30", "type": "ACTUAL"}

protocolSection.identificationModule.nctId

"NCT05702255"

protocolSection.identificationModule.officialTitle

"Effect of Self- Administered Acupressure on Diarrhea Predominant Irritable Bowel Syndrome Patients\u0027 Health Outcomes: a Double Blind- Sham Controlled Randomized Clinical Trial"

protocolSection.statusModule.overallStatus

"COMPLETED"

protocolSection.designModule.phases

["NA"]

protocolSection.statusModule.resultsFirstPostDateStruct

null

Study condition terms

• Irritable Bowel Syndrome With Diarrhea (protocolSection.conditionsModule.conditions)

Interventions recorded in this study

• {'armGroupLabels': ['Active acupoints group'], 'description': 'Participants will receive training (2 sessions, 2 days a part) by a training researcher. Patients will be taught on the acupoints location and the acupressure technique. Participants will be verified for the correct location of the acupoints, acupressure technique and strength. Participants will be instructed to use thumb or middle finger to self- press each acupoint using circular movements. The force of pressing must be sufficiently strong but still within a comfortable range. A lubricant will be uses to decrease friction between the acupoints and the finger. Follow up evaluation will be at the end of the week 2 and week 4 .The training researcher will make weekly calls to remind participants to perform acupressure and to answer questions', 'name': 'Active acupressure', 'type': 'OTHER'} (protocolSection.armsInterventionsModule.interventions[])
• {'armGroupLabels': ['Sham acupoints group'], 'description': 'The same protocol as the active acupressure group.', 'name': 'Sham acuptressure', 'type': 'OTHER'} (protocolSection.armsInterventionsModule.interventions[])

An intervention appearing in a study record does not establish an effect or an approved use.

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