NCT01134588已完成不适用
Assessment of Quality of Life in Disorders of the Pelvic Floor
Centre Hospitalier Universitaire de Nīmes1 个研究点 分布在 1 个国家目标入组 129 人开始时间: 2010年5月1日最近更新:
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 129
- 试验地点
- 1
- 主要终点
- Presence / absence of a completely filled out questionnaire
研究概览
简要总结
The purpose of this study is to compare the touch-screen version of the PFDI-20, PFIQ-7, PISQ 12 and SF-36 french questionnaires to their paper versions. The investigators hypothesize that the percentage of completely filled questionnaires will be higher in the touch-screen version.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Health Services Research
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •the patient has pelvic organ prolapse
- •the patient requires a surgical intervention within the next 4 to 8 weeks
- •the patient understands and reads french
- •the patient is affiliated with a social security system
- •the patient has given consent
排除标准
- •the patient refuses to participate
- •the patient is under guardianship
研究组 & 干预措施
Reference group
Active Comparator
This group will fill out paper questionnaires.
干预措施: Paper questionnaire (Other)
Experimental group
Experimental
This group will fill out touch-screen questionnaires.
干预措施: Touch screen questionnaire (Other)
结局指标
主要结局
Presence / absence of a completely filled out questionnaire
时间窗: 6 months post-op
次要结局
未报告次要终点
研究者
研究点 (1)
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