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A clinical research on the brain-body physiological signal measurements of functional dyspepsia patients to develop prediction algorithm for pattern identification

A clinical research on the brain-body physiological signal measurements of functional dyspepsia patients to develop prediction algorithm for pattern identification

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0009275
Enrollment
100
Registered
2024-03-28
Start date
2024-04-10
Completion date
Unknown
Last updated
2026-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Kyung Hee University Oriental Medicine Hospital at Gangdong
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Adult men and women aged 19 to 65

Exclusion criteria

Exclusion criteria: (1) Individuals diagnosed with organic gastrointestinal disorders such as ulcers, cancer, or inflammatory bowel diseases through gastrointestinal endoscopy within the past 3 years prior to screening. (2) Individuals exhibiting alarm symptoms such as severe weight loss, bloody stools, dysphagia, persistent vomiting, or abdominal pain. (3) Individuals with significant neurological or psychiatric medical history such as major depressive disorder, anxiety disorder, schizophrenia, or those currently suffering from such conditions. (4) Individuals with serious organic conditions affecting physiological signals (e.g., congestive heart failure, angina, myocardial infarction, arrhythmias, valvular disease). (5) Individuals who have taken medications (e.g., anticoagulants, vasodilators, antihypertensives) that may affect physiological signals on the day of physiological signal measurement. (6) Individuals with conditions such as defects in the measurement site (forehead, finger, wrist, chest), skin diseases, or other factors making it difficult to measure physiological signals. (7) Individuals who have undergone gastrointestinal surgery within the past 6 months. (8) Pregnant women. (9) Students, researchers, or staff affiliated with the laboratory conducting the study, including undergraduate and graduate students. (10) Individuals deemed unsuitable for participation in the study by the principal investigator or study coordinator for any other reason.

Design outcomes

Primary

MeasureTime frame
Pulse signal

Secondary

MeasureTime frame
Brain activity signal;Electrocardiogram;Skin conductance response;Nepean Dyspepsia Index score;Questionnaire of Cold-Heat pattern identification;Questionnaire of Deficiency-Excess pattern identification;Phlegm pattern questionnaire;Food retention questionnaire;Questionnaire of spleen qi deficiency pattern;Questionnaire of stomach qi deficiency pattern;State-Trait Anxiety Inventory questionnaire;Beck Depression Inventory-II questionnaire;EuroQol five-dimentional (EQ-5D) questionnaire;Tongue diagnosis;Pulse diagnosis;Abdominal examination;Standard tool for pattern identification for functional dyspepsia

Countries

Korea, Republic of

Contacts

Public ContactHyun Ji Kang

Kyung Hee University

iamhyunji11@naver.com+82-2-961-9616

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 7, 2026