来自研究问卷的负担 关于患者疲劳在定性充血性心力衰竭研究中的负担
Pupalan Iyngkaran1,2, Wania Usmani1, Zahra Bahmani2
1Department of Health and Education, Torrens University Australia, Melbourne, VIC 3000, Australia.
Journal of cardiovascular development and disease
|April 26, 2024
概括
临床试验中的定性研究,特别是充血性心力衰竭 (CHF),可能会给患者和研究人员带来负担. 建议采用较短,经过验证的问卷来收集主观数据,以提高效率和数据质量.
科学领域:
- 翻译性研究方法的研究方法.
- 临床实践中的混合方法研究.
背景情况:
- 定性研究和主观数据对于翻译研究中的假设生成至关重要.
- 仅依赖主观数据的临床试验可能缺乏黄金标准证据的严格性.
- 定性工具可能给患者和研究人员带来很大的负担,影响数据质量.
研究的目的:
- 讨论与主观数据收集和充血性心力衰竭 (CHF) 研究中的患者疲劳相关的挑战.
- 倡导在临床试验中的定性评估中使用更短,经过验证的仪器.
- 突出需要创新的解决方案来减轻研究中主观数据的负担.
主要方法:
- 讨论论文分析了主观数据收集在混合方法研究中的影响.
- 专注于充血性心力衰竭 (CHF) 患者群体与高基线发病率的背景.
- 考虑经过验证的,但又漫长的数据收集工具.
主要成果:
- 主观数据收集对于产生假设至关重要,但与患者和研究人员负担相关的挑战.
- 数据的数量和存储问题可能会导致噪音,并影响初级和二级分析的数据质量.
- 现有的经过验证的仪器可能会耗时,导致疲劳,特别是在像CHF患者这样的脆弱人群中.
结论:
- 在可行的情况下,应优先考虑对验证的定性问卷的更短版本进行临床试验.
- 应避免妥协数据收集要求;重点应放在高效,高质量的数据收集上.
- 投资开发和验证更短的工具或替代解决方案是必要的,以提高主观数据收集在研究中的效率.
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