Abstract
Access to information has been identified as a social determinant of health, influencing knowledge, attitudes, and behaviors that can shape health outcomes. Contraceptive information influences how individuals make decisions about accessing contraceptive care and method use, as well as broader reproductive health trajectories. The recent proliferation of contraceptive misinformation has led to increased research and media attention on this topic. Misinformation from all types of information sources must be understood and addressed by the sexual and reproductive health, rights, and justice field to enable people to make informed, autonomous decisions about contraception based on high-quality, high-integrity evidence. This Research Practice Support aims to guide researchers interested in studying contraceptive misinformation. First, we define key terms related to the information environment and ecosystem, including misinformation, disinformation, and other related concepts. Then, we provide actionable recommendations for each stage of the research process for studies focused on contraceptive misinformation, including study design and ethical considerations, data sources and collection, and dissemination. Scholars are encouraged to consider these recommendations to maximize the impact of their research focused on contraceptive misinformation.