RecruitingNot ApplicableNCT06381921

Objective Integrated Multimodal Electrophysiological Index for the Quantification of Visceral Pain

OIME - Objective Integrated Multimodal Electrophysiological Index for the Quantification of Visceral Pain

Sponsor

University of Connecticut

Enrollment

120 participants

Start Date

Sep 8, 2025

Study Type

INTERVENTIONAL

Conditions

Abdominal Pain

Summary

The objectives of the study are to 1) Conduct telemetric biosignals (EDA, ECG, and EMG) recording in healthy controls and IBS participants experiencing cutaneous and visceral pain; and 2) Validate the OIME index as a biomarker for quantifying pain in IBS participants and its capability to assess the treatment of IBS pain via an ambulatory trial.

Eligibility

Min Age: 18 YearsMax Age: 50 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a behavioral approach called IBS-PPSM intervention for people with abdominal pain. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 50 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALIBS-PPSM intervention

IBS-PPSM intervention includes 10 video modules focused on IBS knowledge and self-management skills plus one-on-one consultation with a nurse for personalized advice about self-monitoring, diet, sleep, and goal setting.