Parents of children newly diagnosed with Autism Spectrum Disorders (ASD) are faced with the daunting task of choosing from numerous autism interventions. At the time this research project began, little was understood about how parents made decisions for their child following the diagnosis. A few groups and organisations, in Australia and overseas, have designed and disseminated resources in various formats to help parents with decision making, but none had been evaluated in a clinical trial that tested the effectiveness of the resource in facilitating this process. Based on a review of the literature, and with consideration for the gap in research on this topic, a mixed methodology project was designed. The project incorporated five studies aiming to: 1) develop an understanding of the information that parents of children with ASD currently use to make intervention decisions, and their information preferences; 2) develop an understanding of parents' decision making processes; 3) evaluate the quality of information most commonly accessed by parents, particularly web-based information; 4) determine how best to help parents understand what interventions are available and how they are classified; and 5) develop and conduct a pilot evaluation of the effectiveness of a decision aid. Study 1 was a cross sectional survey of Autism Advisors, and parents across Australia who were accessing the Helping Children With Autism (HCWA) funding package. The study aimed to obtain a better understanding of how parents made decisions about autism interventions, and which resources they accessed to obtain intervention information. Participants were Autism Advisors (n=13) and parents (n=113) attending initial consultations with an Autism Advisor. After determining that parents frequently accessed the Internet for ASD intervention information, it was considered important to investigate the quality of information parents were likely to be finding. Study 2 analysed the quality of health information in a sample of autism-related websites using a valid and reliable health information evaluation tool called DISCERN. This study found that websites were of variable quality and frequently lacked references to research evidence. Study 3 involved conducting focus groups and individual interviews with parents (n = 23) whose children were aged under 18 years and diagnosed with an ASD.iii The aim was to further investigate parents' decision making processes and further explore the various formats and sources of information used. This study revealed that parents engaged in both a pragmatic and emotional journey and gained confidence over time in relation to their decision making regarding interventions for their child. Study 4 involved developing a web-based decision aid informed by the results of the first three studies, and with consideration for the literature on shared decision making, health literacy and patient education.The resource aimed to assist parents to make better-informed decisions about autism interventions, with considera...