Accessing the Clarity and Acceptability of Recruitment Materials for a Study on Thoracic Aortic Disease Surveillance: A Qualitative Feasibility Study.
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 30
- 试验地点
- 1
研究概览
简要总结
People who are invited to take part in health research are usually given written information, such as invitation letters, and information sheets. These documents are essential because they help people understand what the study involves and decide whether they want to take part. However, many studies have shown that research information is often too complex, too long, or written in technical language. This can make it difficult for people to fully understand the study and give informed consent.
This study aims to assess how clear, accessible, and acceptable draft research documents are for a proposed future doctoral study related to thoracic aortic disease. Thoracic aortic disease is a long-term condition that requires regular monitoring, and people in surveillance programmes may be invited to take part in research. It is therefore important that study information is clear, sensitive, and easy to understand.
In this study, staff and students from the University's School of Health Sciences will be asked to review draft recruitment materials. These materials include a study invitation, an information sheet, and interview guide. Participants will be asked to give feedback on how easy the documents are to read, whether the information is clear, whether the tone feels appropriate, and whether the amount of information feels reasonable.
The study will also use a standard readability tool to assess whether the documents are written at a level suitable for the public.
This research does not involve patients and is considered low risk. Its purpose is to improve research materials before they are used with patients, helping to support informed consent, reduce confusion, and improve ethical and inclusive research practice in future studies.
详细描述
BACKGROUND AND RATIONALE:
Recruitment materials such as information sheets, consent forms, and questionnaires help people decide whether they want to take part in research. These documents are important because they explain what the study involves and help people make an informed choice. If the information is too technical, too long, or given at the wrong time, people may feel confused, anxious, or decide not to take part.
People with thoracic aortic disease (TAD) attend regular hospital appointments for monitoring and imaging. During these visits, they may be invited to take part in research studies. These moments can be stressful, and patients may find it difficult to process complex research information.
This study will explore how recruitment materials are written, when they are given to patients, and how patients understand them in the context of thoracic aortic disease surveillance. The aim is to identify ways to make research information clearer, more appropriate, and easier to understand, so that people can make informed decisions about participation.
The findings will be used to improve recruitment materials and strategies for a future doctoral research study. This will help support ethical recruitment, reduce participant burden, and promote fair and inclusive participation in thoracic aortic disease research.
研究设计
- 研究类型
- Observational
- 观察模型
- Other
- 时间视角
- Cross Sectional
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Adults aged 18 years or older
- •Able to read and understand English
排除标准
- •Individuals under 18
- •Individuals unable to provide informed consent
- •Individuals unable to read or understand English
