Postpartum Pelvic Floor Rehabilitation and Information Provided by the Health Care Providers (PPFR)
Opinion Survey on Postpartum Pelvic Floor Rehabilitation According to the Quality of Information Provided by the Health Care Providers
研究概览
详细说明
Postpartum Pelvic Floor Rehabilitation is an important central stage of the postpartum period. It allows, if it is well done, to reduce complications related to childbirth, (pelvic floor disorders: urinary, sexual or anal disorders ) and to increase quality of life of women in postpartum period.
But, what about the woman's opinion and experience of PPFR? Previous studies have evaluated the effectiveness of PPFR but not the woman's experience.
It is interesting to evaluate the experience of PPFR according to the information given by the health care providers. There is to improve medical practice and to give the right information in at the right time to the women
研究类型
注册 (预期的)
联系人和位置
学习联系方式
- 姓名:Agnès Dorion
- 电话号码:+33 251446380
- 邮箱:agnes.dorion@chd-vendee.fr
学习地点
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La Roche sur Yon、法国、85000
- 招聘中
- Departmental Hospital Center of Vendee
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接触:
- Guillaume DUCARME
- 邮箱:guillaume.ducarme@chd-vendee.fr
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首席研究员:
- Guillaume Ducarme, Dr
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-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
研究人群
描述
Inclusion Criteria:
- All women undergoing postpartum pelvic floor rehabilitation at the Departmental Hospital Center of Vendee
Exclusion Criteria:
- Refusal to participate in the study
- Patient did not complete all her PPFR sessions at the Departmental Hospital Center of Vendee
- Patient unable to understand the protocol, read the information note and answer the questionnaires
- Patient under tutelage, curatorship, mandate of future protection, family habilitation
学习计划
研究是如何设计的?
设计细节
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
---|---|---|
Overall experience of the PPFR according to information given by the health care providers
大体时间:through study completion, an average of 5 weeks
|
Self-evaluation of the overall experience of postpartum pelvic floor rehabilitation
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through study completion, an average of 5 weeks
|
合作者和调查者
调查人员
- 首席研究员:Guillaume DUCARME, Dr、Departmental Hospital Center of Vendee
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (预期的)
研究完成 (预期的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- CHD21_0027
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.
功能恢复的临床试验
-
Swansea University完全的
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Scripps Translational Science Institute完全的