TY - JOUR T1 - Comparing the effectiveness of a crowdsourced video and a social marketing video in promoting condom use among Chinese men who have sex with men: a study protocol JF - BMJ Open JO - BMJ Open DO - 10.1136/bmjopen-2015-010755 VL - 6 IS - 10 SP - e010755 AU - Chuncheng Liu AU - Jessica Mao AU - Terrence Wong AU - Weiming Tang AU - Lai Sze Tso AU - Songyuan Tang AU - Ye Zhang AU - Wei Zhang AU - Yilu Qin AU - Zihuang Chen AU - Wei Ma AU - Dianming Kang AU - Haochu Li AU - Meizhen Liao AU - Katie Mollan AU - Michael Hudgens AU - Barry Bayus AU - Shujie Huang AU - Bin Yang AU - Chongyi Wei AU - Joseph D Tucker Y1 - 2016/10/01 UR - http://bmjopen.bmj.com/content/6/10/e010755.abstract N2 - Introduction Crowdsourcing has been used to spur innovation and increase community engagement in public health programmes. Crowdsourcing is the process of giving individual tasks to a large group, often involving open contests and enabled through multisectoral partnerships. Here we describe one crowdsourced video intervention in which a video promoting condom use is produced through an open contest. The aim of this study is to determine whether a crowdsourced intervention is as effective as a social marketing intervention in promoting condom use among high-risk men who have sex with men (MSM) and transgender male-to-female (TG) in China.Method We evaluate videos developed by crowdsourcing and social marketing. The crowdsourcing contest involved an open call for videos. Entries were judged on capacity to promote condom use, to be shareable or ‘go viral’ and to give value to the individual. 1170 participants will be recruited for the randomised controlled trial. Participants need to be MSM age 16 and over who have had condomless anal sex in the last 3 months. Recruitment will be through an online banner ad on a popular MSM web page and other social media platforms. After completing an initial survey, participants will be randomly assigned to view either the social marketing video or the crowdsourcing video. Follow-up surveys will be completed at 3 weeks and 3 months after initial intervention to evaluate condomless sex and related secondary outcomes. Secondary outcomes include condom social norms, condom negotiation, condom self-efficacy, HIV/syphilis testing, frequency of sex acts and incremental cost.Ethics and dissemination Approval was obtained from the ethical review boards of the Guangdong Provincial Center for Skin Diseases and STI Control, UNC and UCSF. The results of this trial will be made available through publication in peer-reviewed journals.Trial registration number NCT02516930. ER -