MHealth Intervention of HIV and STDs Partner Notification for MSM
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ClinicalTrials.gov Identifier: NCT04349748 |
Recruitment Status :
Not yet recruiting
First Posted : April 16, 2020
Last Update Posted : May 27, 2020
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Condition or disease | Intervention/treatment | Phase |
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HIV/AIDS Sexually Transmitted Diseases Prevention | Behavioral: Health education, and regular HIV and STDs testing prompting service Behavioral: Health status inquiry through app (partner notification) | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 6172 participants |
Allocation: | Randomized |
Intervention Model: | Crossover Assignment |
Intervention Model Description: | This study is not a conventional crossover design,we use a pragmatic stepped-wedge cluster-randomised design.The study lasts for 2.5 years, which is divided to five continuous observation periods (every six months).The sixteen districts are assigned to four arms randomly.Four arms began recruiting participants at the same time,and at the first observation period,all groups were given health education and regular HIV and STDs testing prompting service,the two services above are given continuously for five observation periods.At the second observation period,the first group is given permission to query health status (partner notification) through app,but the other three groups do not.At every observation period after that (the third to fifth observation period),the three groups will be given permission to query health status one by one.Once a group is given the permission,it is retained until the end of study. |
Masking: | Single (Outcomes Assessor) |
Masking Description: | Because partner notification is a kind of behavioral intervention, participants know what intervention they receive. However, we take efforts to reduce the bias caused by the non-blind design. At the beginning of the research, participants, care providers, and researchers who participate in participants management will not know the randomized scheme. The partner notification will be opened to participants sequentially by the predetermined computer program, and does not need care providers and researchers to implement the intervention manually. The care providers and researchers do not know the implementation of partner notification unless the participants tell them whether they can use the function on their own initiative. Even the care providers know that, the operation and results of the HIV and STDs testing will not be affected. At last, the outcomes assessors do not know the randomized scheme in data analysis. |
Primary Purpose: | Prevention |
Official Title: | The Effect of Providing mHealth Intervention of Partner Notification to Protect MSM From HIV and Sexually Transmitted Diseases Infection: a Pragmatic Stepped Wedge Cluster Randomized Controlled Trial |
Estimated Study Start Date : | July 1, 2020 |
Estimated Primary Completion Date : | December 31, 2022 |
Estimated Study Completion Date : | June 30, 2023 |

Arm | Intervention/treatment |
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Experimental: Group 1
The group is given health education, regular HIV and STDs testing prompting service in the whole study, and permission to query health status (partner notification) through app from the second observation period. HIV and STDs testing and questionnaire are given to the participants when they receive the testing service.
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Behavioral: Health education, and regular HIV and STDs testing prompting service
Health education through app for once a week, and regular HIV and STDs testing prompting service (every month through app) are given to the participants at the beginning of the study and last for the whole five observation periods. Behavioral: Health status inquiry through app (partner notification) The permission to query health status through app (partner notification) is given to participants (participants can query their potential sexual partner's status of HIV, syphilis, hepatitis B, and hepatitis C respectively through app) at the specific observation period,and the permission is retained until the end of study. |
Experimental: Group 2
The group is given health education, regular HIV and STDs testing prompting service in the whole study, and permission to query health status (partner notification) through app from the third observation period. HIV and STDs testing and questionnaire are given to the participants when they receive the testing service.
|
Behavioral: Health education, and regular HIV and STDs testing prompting service
Health education through app for once a week, and regular HIV and STDs testing prompting service (every month through app) are given to the participants at the beginning of the study and last for the whole five observation periods. Behavioral: Health status inquiry through app (partner notification) The permission to query health status through app (partner notification) is given to participants (participants can query their potential sexual partner's status of HIV, syphilis, hepatitis B, and hepatitis C respectively through app) at the specific observation period,and the permission is retained until the end of study. |
Experimental: Group 3
The group is given health education, regular HIV and STDs testing prompting service in the whole study, and permission to query health status (partner notification) through app from the fourth observation period. HIV and STDs testing and questionnaire are given to the participants when they receive the testing service.
|
Behavioral: Health education, and regular HIV and STDs testing prompting service
Health education through app for once a week, and regular HIV and STDs testing prompting service (every month through app) are given to the participants at the beginning of the study and last for the whole five observation periods. Behavioral: Health status inquiry through app (partner notification) The permission to query health status through app (partner notification) is given to participants (participants can query their potential sexual partner's status of HIV, syphilis, hepatitis B, and hepatitis C respectively through app) at the specific observation period,and the permission is retained until the end of study. |
Experimental: Group 4
The group is given health education, regular HIV and STDs testing prompting service in the whole study, and permission to query health status (partner notification) through app from the fifth observation period. HIV and STDs testing and questionnaire are given to the participants when they receive the testing service.
|
Behavioral: Health education, and regular HIV and STDs testing prompting service
Health education through app for once a week, and regular HIV and STDs testing prompting service (every month through app) are given to the participants at the beginning of the study and last for the whole five observation periods. Behavioral: Health status inquiry through app (partner notification) The permission to query health status through app (partner notification) is given to participants (participants can query their potential sexual partner's status of HIV, syphilis, hepatitis B, and hepatitis C respectively through app) at the specific observation period,and the permission is retained until the end of study. |
- HIV positive seroconversion rate (HIV incidence) [ Time Frame: through study completion, an average of six months ]The number of HIV positive seroconversions divided by the total number of person-years.
- Additional cost of the intervention [ Time Frame: through study completion, an average of six months ]The total cost and average cost for per participant of the integrated intervention model and each additional intervention/service based on the existing HIV prevention measures provided as before.
- Syphilis positive seroconversion rate (Syphilis incidence) [ Time Frame: through study completion, an average of six months ]The number of syphilis seroconversions divided by the total number of person-years.
- Hepatitis B positive seroconversion rate (Hepatitis B incidence) [ Time Frame: through study completion, an average of six months ]The number of hepatitis B seroconversions divided by the total number of person-years.
- Hepatitis C positive seroconversion rate (Hepatitis C incidence) [ Time Frame: through study completion, an average of six months ]The number of hepatitis C seroconversions divided by the total number of person-years.
- HIV and related diseases transmission among social networks [ Time Frame: through study completion, an average of 1 year ]Based on the partner notification information, we will construct the transmission networks of HIV and other STDs (syphilis, hepatitis B, and hepatitis C) among participants, and analyze the characteristics of these networks and factors associated with transmission of these diseases.
- Testing adherence [ Time Frame: through study completion, an average of 1 year ]The proportion of participants whose every adjacent testing interval is no more than 3 months as recommended by China CDC.
- Additional cost for finding per seroconversion [ Time Frame: through study completion, an average of six months ]The total additional cost of the integrated intervention model based on the existing HIV prevention measures provided as before divided by the total number of the HIV and STDs seroconversions.
- Frequency of utilization for each intervention/service [ Time Frame: through study completion, an average of six months ]The total frequency and average frequency for per participant of utilization for each intervention/service, such as health education, partner notification, HIV and STDs testing and so on.
- Satisfaction of the interventions and services [ Time Frame: through study completion, an average of six months ]This indicator is measured by the follow-up questionnaires as the degree of satisfaction for participants of HIV and STDs testing service, health education, partner notification and other app's functions.
- Knowledge of HIV and related STDs [ Time Frame: through study completion, an average of six months ]This indicator is measured by the baseline and follow-up questionnaires, and we use the score of knowledge questions in the questionnaires to represent participants' level of knowledge.
- Attitudes of HIV and STDs testing, safe sexual behaviors and partner notification [ Time Frame: through study completion, an average of six months ]The attitudes are collected by these questions in the baseline and follow-up questionnaires.
- Sexual behaviors [ Time Frame: through study completion, an average of six months ]They are measured by questionnaires, including questions about the number of different kinds of sexual partners, frequency of anal sex, condom use, and partner notification implementation.
- Substance use behaviors [ Time Frame: through study completion, an average of six months ]This indicator is measured by questionnaires about participants' usage about methamphetamine, heroin, ecstasy, and some other sex-promoting drugs.
- Psychological status [ Time Frame: through study completion, an average of six months ]SAS (self-rating anxiety) scale and SDS (self-rating depression) scale are used to measure participants' psychological status through questionnaires. The higher scores of the two scares mean the worse outcomes.
- Referral rate of HIV and related STDs [ Time Frame: through study completion, an average of six months ]The proportion of new HIV and STDs infections who have received treatment.

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Ages Eligible for Study: | 15 Years and older (Child, Adult, Older Adult) |
Sexes Eligible for Study: | Male |
Accepts Healthy Volunteers: | Yes |
Inclusion criteria:
- biologically male,
- had oral or anal sex with men at least once during their lifetime,
- 15 years of age or older,
- had no difficulty using a mobile phone,
- willing to provide their mobile phone numbers to serve as the unique identification numbers of the app's self-query and partner notification functions,
- willing to use the app's function modules,
- willing to complete the questionnaire for the research,
- willing to continuously receive HIV and STDs testing and consulting services provided by the CBO our research setting at,
- willing to complete the informed consent document.
Exclusion criteria:
1.had serious physical disabilities or mental diseases.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04349748
Contact: Zhongwei Jia, Prof. PhD | +86-10-82802457 | urchinjj@163.com | |
Contact: Xiangyu Yan, PhD | +86-18380205261 | yanxiangyu@bjmu.edu.cn |
Principal Investigator: | Zhongwei Jia, Prof. PhD | National Institute on Drug Dependence, Peking University,China |
Publications:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: | ZhongweiJia, Professor, Director of Center for Drug Abuse Control and Prevention, National Institute on Drug Dependence, China |
ClinicalTrials.gov Identifier: | NCT04349748 |
Other Study ID Numbers: |
NIDD-HIV |
First Posted: | April 16, 2020 Key Record Dates |
Last Update Posted: | May 27, 2020 |
Last Verified: | May 2020 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | Yes |
Plan Description: |
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Supporting Materials: |
Study Protocol Statistical Analysis Plan (SAP) Informed Consent Form (ICF) Clinical Study Report (CSR) Analytic Code |
Time Frame: | Two years after the end of the trial |
Access Criteria: | Data applicants should send email to PI. Real personal basic information (name, unit, title, etc.), detailed description of required data (required variables,etc.), and research plan should be included in the email. Our team will discuss the research proposal and reply as soon as possible |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
HIV/AIDS sexually transmitted disease (STD) men who have sex with men (MSM) |
partner notification mHealth application stepped wedge cluster randomized controlled trial |
Acquired Immunodeficiency Syndrome HIV Infections Sexually Transmitted Diseases Blood-Borne Infections Communicable Diseases Infections Sexually Transmitted Diseases, Viral Lentivirus Infections |
Retroviridae Infections RNA Virus Infections Virus Diseases Slow Virus Diseases Immunologic Deficiency Syndromes Immune System Diseases Disease Attributes Pathologic Processes |