15 research outputs found

    SurveyMan: Programming and Automatically Debugging Surveys

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    Surveys can be viewed as programs, complete with logic, control flow, and bugs. Word choice or the order in which questions are asked can unintentionally bias responses. Vague, confusing, or intrusive questions can cause respondents to abandon a survey. Surveys can also have runtime errors: inattentive respondents can taint results. This effect is especially problematic when deploying surveys in uncontrolled settings, such as on the web or via crowdsourcing platforms. Because the results of surveys drive business decisions and inform scientific conclusions, it is crucial to make sure they are correct. We present SurveyMan, a system for designing, deploying, and automatically debugging surveys. Survey authors write their surveys in a lightweight domain-specific language aimed at end users. SurveyMan statically analyzes the survey to provide feedback to survey authors before deployment. It then compiles the survey into JavaScript and deploys it either to the web or a crowdsourcing platform. SurveyMan's dynamic analyses automatically find survey bugs, and control for the quality of responses. We evaluate SurveyMan's algorithms analytically and empirically, demonstrating its effectiveness with case studies of social science surveys conducted via Amazon's Mechanical Turk.Comment: Submitted version; accepted to OOPSLA 201

    3 years of liraglutide versus placebo for type 2 diabetes risk reduction and weight management in individuals with prediabetes: a randomised, double-blind trial

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    Background: Liraglutide 3·0 mg was shown to reduce bodyweight and improve glucose metabolism after the 56-week period of this trial, one of four trials in the SCALE programme. In the 3-year assessment of the SCALE Obesity and Prediabetes trial we aimed to evaluate the proportion of individuals with prediabetes who were diagnosed with type 2 diabetes. Methods: In this randomised, double-blind, placebo-controlled trial, adults with prediabetes and a body-mass index of at least 30 kg/m2, or at least 27 kg/m2 with comorbidities, were randomised 2:1, using a telephone or web-based system, to once-daily subcutaneous liraglutide 3·0 mg or matched placebo, as an adjunct to a reduced-calorie diet and increased physical activity. Time to diabetes onset by 160 weeks was the primary outcome, evaluated in all randomised treated individuals with at least one post-baseline assessment. The trial was conducted at 191 clinical research sites in 27 countries and is registered with ClinicalTrials.gov, number NCT01272219. Findings: The study ran between June 1, 2011, and March 2, 2015. We randomly assigned 2254 patients to receive liraglutide (n=1505) or placebo (n=749). 1128 (50%) participants completed the study up to week 160, after withdrawal of 714 (47%) participants in the liraglutide group and 412 (55%) participants in the placebo group. By week 160, 26 (2%) of 1472 individuals in the liraglutide group versus 46 (6%) of 738 in the placebo group were diagnosed with diabetes while on treatment. The mean time from randomisation to diagnosis was 99 (SD 47) weeks for the 26 individuals in the liraglutide group versus 87 (47) weeks for the 46 individuals in the placebo group. Taking the different diagnosis frequencies between the treatment groups into account, the time to onset of diabetes over 160 weeks among all randomised individuals was 2·7 times longer with liraglutide than with placebo (95% CI 1·9 to 3·9, p<0·0001), corresponding with a hazard ratio of 0·21 (95% CI 0·13–0·34). Liraglutide induced greater weight loss than placebo at week 160 (–6·1 [SD 7·3] vs −1·9% [6·3]; estimated treatment difference −4·3%, 95% CI −4·9 to −3·7, p<0·0001). Serious adverse events were reported by 227 (15%) of 1501 randomised treated individuals in the liraglutide group versus 96 (13%) of 747 individuals in the placebo group. Interpretation: In this trial, we provide results for 3 years of treatment, with the limitation that withdrawn individuals were not followed up after discontinuation. Liraglutide 3·0 mg might provide health benefits in terms of reduced risk of diabetes in individuals with obesity and prediabetes. Funding: Novo Nordisk, Denmark

    Creating Conversational Characters Using Question Generation Tools

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    This article describes a new tool for extracting question-answer pairs from text articles, and reports three experiments which investigate how suitable this technique is for supplying knowledge to conversational characters. Experiment 1 demonstrates the feasibility of our method by creating characters for 14 distinct topics and evaluating them using hand-authored questions. Experiment 2 evaluates three of these characters using questions collected from naive participants, showing that the generated characters provide full or partial answers to about half of the questions asked. Experiment 3 adds automatically extracted knowledge to an existing, hand-authored character, demonstrating that augmented characters can answer questions about new topics but with some degradation of the ability to answer questions about topics that the original character was trained to answer. Overall, the results show that question generation is a promising method for creating or augmenting a question answering conversational character using an existing text
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