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Feasibility Study of Continuous Intervention with Designated Treatment Application for NASH (Non-Alcoholic Steatohepatitis) Patients

Feasibility Study of Continuous Intervention with Designated Treatment Application for NASH (Non-Alcoholic Steatohepatitis) Patients - Continuous Intervention of Application for NASH patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000025912
Enrollment
10
Registered
2017-01-31
Start date
2016-09-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Non-Alcoholic Steatohepatitis

Interventions

Intervention and aid application for improvement of non-alcoholic steatohepatitis

Sponsors

Department of Gastroenterology, The University of Tokyo
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: patients diagnosed as non-alcoholic steatohepatitis by clinical examinations including imageinspection and who agree to participate in the study after enough explanation about the study.

Exclusion criteria

Exclusion criteria: exclusion criteria 1. a patient does not agree 2. a patient who the attending physician think is does not seem able to use a smartphone. 3. pregnant patients. 4. patients with comorbid hepatitis (e.g., viral hepatitis, autoimmune hepatitis)

Design outcomes

Primary

MeasureTime frame
The use or achievement rate of program provided by application

Countries

Japan

Contacts

Public ContactMasaya Sato

The University of Tokyo Department of Clinical Laboratory Medicine , Department of Gastroenterology

satoma-tky@umin.ac.jp+81-3-3815-5411

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026