Serious Game Interventions to Reduce Viral Hepatitis C Among PLWH-MSM

Sponsor
National Taiwan University Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05751889
Collaborator
(none)
1,320
2
34.3

Study Details

Study Description

Brief Summary

The study is aimed to provide high-risk, HIV-infection, men who have sex with men (MSM) with healthcare education regarding viral hepatitis C, through either serious game intervention or traditional online health education. After the education, each participants will be followed for 48 weeks and the change of risky sexual behaviors, acquisition of HCV and other STIs will be followed during the study periods.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Serious Game
  • Behavioral: Traditional Health Education
N/A

Detailed Description

High-risk MSM living with HIV were participated in our study will be assigned (by randomization) to either:

  1. Serious game intervention: 1 single session of serious game for the participants to play (estimation to take 25-40 minutes). Hepatitis C virus (HCV)-related healthcare informations, including the severity of illness, route of transmission, preventive strategies and treatment options, would be embedded in the game.

  2. Traditional online health education (reading materials): 1 single session of healthcare education regarding HCV (with similar contents) will be provided.

After the healthcare intervention, each participants will be followed for 48 weeks. Assessment of risky sexual practice (by questionnaire), test of plasma HCV RNA and serological test of syphilis (optional), and detection of sexually-transmitted bacterial pathogens (optional) will be performed at the enrollment and then every 12 weeks during the observation.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
1320 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Two groups will be assigned to either interventional (serious game intervention) or comparator (traditional health education).Two groups will be assigned to either interventional (serious game intervention) or comparator (traditional health education).
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Reducing the Risk of Viral Hepatitis C and Other Sexually Transmitted Infections Among People Living With HIV Who Are Men Who Have Sex With Men: Efficacy of Serious Game Interventions
Anticipated Study Start Date :
Feb 20, 2023
Anticipated Primary Completion Date :
Dec 31, 2025
Anticipated Study Completion Date :
Dec 31, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Serious Game Intervention

Provided with a single session serious game intervention regarding HCV and safe sexual practice.

Behavioral: Serious Game
Serious Game embedded with healthcare information regarding HCV and safe sexual practice.

Active Comparator: Traditional Health Education

Provided with a single session of traditional online healthcare education regarding HCV and safe sexual practice.

Behavioral: Traditional Health Education
Reading materials regarding HCV and safe sexual practice.

Outcome Measures

Primary Outcome Measures

  1. HCV incidence [48 weeks]

    The incidence rate of HCV acquisition between both arms. HCV RNA would be tested for each participants every 3 months during follow-up, and the incidence rate is calculated as following: new cases of HCV viremia / person-time of follow-up.

Secondary Outcome Measures

  1. STI incidence [48 weeks]

    The incidence of sexually-transmitted infection between both arms. Consultation and diagnosis of STI would be performed for each participants every 3 months during follow-up, and the incidence rate is calculated as following: new cases of STI / person-time of follow-up.

  2. The frequency of condom use and sexualized drug use [At weeks 12, 24 and 48 of observation]

    The frequency engaging in condomless sex and the use of sexualized drugs (within the past 3 months) will be assessed for each participant at the enrollment, week 12, 24 , and 48. We would compare the change these behaviors at week 12, 24 and 48 to the baseline to see if there are difference between the two arms.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • High-risk MSM living with HIV, defined as:
  1. Had prior HCV infection, and had cleared HCV through treatment or spontaneously

  2. Had any STI within the past 12 months

  3. Had any unexplained elevation of liver transaminase in the past 6 months

  4. Had at least 1 unprotected anal sex during the past 6 months

  • Being able to use mobile smartphone and understand study materials

  • Repeat entry of study is permitted, but the interval between health education intervention should >52 weeks.

Exclusion Criteria:
  • HCV RNA positive and yet clear virus (nor reaching SVR12).

  • Admission for any acute illness (including AIDS-defining conditions)

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • National Taiwan University Hospital

Investigators

  • Principal Investigator: Chien-Ching Hung, PhD, National Taiwan University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
National Taiwan University Hospital
ClinicalTrials.gov Identifier:
NCT05751889
Other Study ID Numbers:
  • 202212073RINC
First Posted:
Mar 2, 2023
Last Update Posted:
Mar 2, 2023
Last Verified:
Jan 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by National Taiwan University Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 2, 2023