NCT03248934已完成不适用
Delineating the Concurrent Validity and Diagnostic Accuracy of a Patient Performed Examination for Patients With Intra-Articular Hip Pain: A Proof of Concept Study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 80
- 试验地点
- 2
- 主要终点
- Sensitivity
研究概览
简要总结
The primary objective of this study is evaluate the diagnostic accuracy of a patient self-administered clinical examination of the hip compared with a traditional clinical examination (i.e. index test).
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age: 18-80 years
- •Seeking care for hip related pain and/or clicking, catching, giving way or stiffness
- •Able to sign or verbalize study consent
- •No other medical conditions (e.g. gynecological or urinary pathology) that may affect study results
- •English speaking
排除标准
- •Patients with primary lumbar spine, sacro-iliac or other non-hip related pain as determined with clinical examination
- •Previous hip surgery
- •Previous hip injury that would normally exclude from examination as standard practice
- •Unable to sign or verbalize consent
- •Other non-musculoskeletal pathology that may affect study results (e.g. gynecological or urinary pathology)
- •Non-English speaking
结局指标
主要结局
Sensitivity
时间窗: End of clinician examination, 20 minutes
As measured by a questionnaire evaluating the diagnostic test's ability to identify a positive finding when the targeted diagnosis is actually present (i.e. true positive).
次要结局
- Diagnostic accuracy measure of positive likelihood ratio(End of clinician examination, 20 minutes)
- Specificity(End of clinician examination, 20 minutes)
- Diagnostic accuracy measure of negative likelihood ratio(End of clinician examination, 20 minutes)
- Diagnostic accuracy measure of post-test probabilities(End of clinician examination, 20 minutes)
研究者
研究点 (2)
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