Abdominal pain that is relieved by defecation
Conditions
Interventions
For the intervention group, the subjects will receive the survey and useful information for the abdominal symptoms during the experiment biweekly (total 3 times)
For the control group, the subject w
Sponsors
Chitose Laboratory Corp.
Kirin Holdings Company, Limited
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (1) Subjects whose age is between 20 and 49 years old (2) Subjects who are currently having abdominal symptoms (3) Subjects who do not have infectious diseases of the respiratory tract (4) Subjects who can answer the online survey using their own digital device (5) Subjects who agree to participate in the surveys relating to their own health as well as the follow-up survey (total 4 surveys) (6) Subjects who agree to learn about their unknown health status including being judged by doctors (7) Subjects who agree to participate in the study
Exclusion criteria
Exclusion criteria: (1) Subjects who had irritable bowel syndrome (2) Subjects who are currently seeing a doctor due to the abdominal symptoms
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Validation of the effective behavioral change approaches for medical treatments | — |
Countries
Japan
Contacts
Public ContactYuki Kawaharada
Chitose Laboratory Corp. Tech & Biz Development Div.
Outcome results
None listed