Randomized Controlled Trials (RCTs) are rigorous clinical studies crucial for reliable decision-making, but their credibility can be compromised by bias. The Cochrane Risk of Bias tool (RoB 2) assesses this risk, yet manual assessments are time-consuming and labor-intensive. Previous approaches have employed Large Language Models (LLMs) to automate this process. However, they typically focus on manually crafted prompts and a restricted set of simple questions, limiting their accuracy and generalizability. Inspired by the human bias assessment process, we propose RoBGuard, a novel framework for enhancing LLMs to assess the risk of bias in RCTs. Specifically, RoBGuard integrates medical knowledge-enhanced question reformulation, multimodal document parsing, and multi-expert collaboration to ensure both completeness and accuracy. Additionally, to address the lack of suitable datasets, we introduce two new datasets: RoB-Item and RoB-Domain. Experimental results demonstrate RoBGuard’s effectiveness on the RoB-Item dataset, outperforming existing methods.

With the Generative Pre-trained Transformer 3.5 (GPT-3.5) exhibiting remarkable reasoning and comprehension abilities in Natural Language Processing (NLP), most Question Answering (QA) research has primarily centered around general QA tasks based on GPT, neglecting the specific challenges posed by Complex Table QA. In this paper, we propose to incorporate GPT-3.5 to address such challenges, in which complex tables are reconstructed into tuples and specific prompt designs are employed for dialogues. Specifically, we encode each cell’s hierarchical structure, position information, and content as a tuple. By enhancing the prompt template with an explanatory description of the meaning of each tuple and the logical reasoning process of the task, we effectively improve the hierarchical structure awareness capability of GPT-3.5 to better parse the complex tables. Extensive experiments and results on Complex Table QA datasets, i.e., the open-domain dataset HiTAB and the aviation domain dataset AIT-QA show that our approach significantly outperforms previous work on both datasets, leading to state-of-the-art (SOTA) performance.