Feasibility Study of Continuous Intervention with Designated Treatment Application for NASH (Non-Alcoholic Steatohepatitis) Patients
Not Applicable
- Conditions
- on-Alcoholic Steatohepatitis
- Registration Number
- JPRN-UMIN000025912
- Lead Sponsor
- Department of Gastroenterology, The University of Tokyo
- Brief Summary
Since one patient was lost to follow-up, the comparison between pre- and post-intervention values was performed for 8 patients. A post-intervention weight reduction was observed in 7 patients, and this weight reduction was statistically significant (p=0.02).Normalization of the ALT level (<30 U/L) was observed in two patients.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 9
Inclusion Criteria
Not provided
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)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method