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Health Promotion and Management for Hepatitis B Carriers

National Taiwan University logo

National Taiwan University

Status

Unknown

Conditions

Chronic Hepatitis B

Treatments

Behavioral: standardized exercise program and dietary counseling

Study type

Interventional

Funder types

Other

Identifiers

NCT01065363
200906036R

Details and patient eligibility

About

The investigators propose a project of preventive medicine with concern of local context in Taiwan. The target population includes all staff and faculty members, students, and alumni of a university in Northern Taiwan, with chronic hepatitis B infection. The intervention of this project includes standardized lectures, sports courses, nutrition courses, and an information platform. The investigators will evaluate the efficacy after the intervention, like the reduction of hepatitis B viral load and the associated anthropometric parameters. The results of this project will be initially served as a pilot study for this cohort, and applicated as a promising basis for health promotion.

Enrollment

160 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participants were recruited from students, alumni, faculty and staff members with chronic HBV infection (positive HBsAg serostatus ≥6 months) in a university of northern Taiwan from August 1, 2009 to July 01, 2010. Only participants aged 18 and older were included.

Exclusion criteria

  • Excluded were:

    • (a) those who had been diagnosed as chronic liver diseases like chronic hepatitis C infection (Anti-HCV (+)), autoimmune hepatitis, Wilson disease, alcoholic liver diseases, drug-related hepatitis, decompensated liver diseases, cirrhosis, or malignant hepatic tumors;
  • (b) those who had undergone liver transplantation or major operations for liver except cholecystectomy;

  • (c) men who consumed more than 30 gram of alcohol per week or women who consumed more than 20 gram of alcohol per week;

  • (d) women who were pregnant;

  • (e) those who had current medications for any types of chronic diseases except for hyperglycemia, elevated blood pressure, or dyslipidemia within six months.

Trial design

Primary purpose

Prevention

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

160 participants in 1 patient group

Lifestyle conseling
Experimental group
Treatment:
Behavioral: standardized exercise program and dietary counseling

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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