Improving Uroflowmetry Interpretability: Evaluating the Impact of Patient Reminder Systems
2026年8月13日 更新者:Lisa Hickman、Ohio State University
The purpose of this study is to evaluate the impact of pre-procedure patient reminder systems on patient satisfaction, preparedness, and anxiety among patients undergoing urodynamics studies.
The rate of successful procedure completion will be compared between a prospective intervention group and a historical control group to determine whether the intervention improves procedural success and healthcare delivery.
研究概览
研究类型
介入性
注册 (估计的)
162
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习联系方式
- 姓名:Lisa Hickman, MD
- 电话号码:614-814-8205
- 邮箱:Lisa.Hickman@osumc.edu
研究联系人备份
- 姓名:Ashka Shah
- 邮箱:Ashka.Shah@osumc.edu
学习地点
-
-
Ohio
-
Columbus、Ohio、美国、43210
- 招聘中
- Ohio State University Wexner Medical Center
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接触:
- Lisa Hickman, MD
- 电话号码:614-814-8205
- 邮箱:Lisa.Hickman@osumc.edu
-
-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
不
描述
Inclusion Criteria
- Age 18 years or older
- Sex assigned at birth: Female.
- English-speaking
- Scheduled to undergo a urodynamics study at the OSU Upper Arlington Outpatient Clinic, OSU New Albany Outpatient Clinic, or OSU Eye and Ear Institute
- Ability to access a telephone
- Active MyChart account
- Ability to provide informed consent
- Documented post-residual volume of less than 150 mL
- Ability to be reached by telephone after three call attempts
- Negative point-of-care urinary tract infection on the day of the scheduled procedure (SOC)
Exclusion criteria:
- Under 18 years of age
- Patients with structural causes of urinary retention/incomplete bladder emptying (defined as a post-void residual >150ml) or a positive point-of-care urinary tract infection on the day of the procedure.
- Men are excluded as the population of interest is the female urogynecology population in both urology and obstetrics and gynecology.
- Patients without access to a telephone or an active MyChart account are excluded because the intervention relies on telephone calls and electronic messaging for delivery of pre-procedure education and reminders.
- Individuals who cannot be reached by telephone are excluded because they cannot receive the intervention.
- Non-English speaking individuals are excluded because they will not be able to receive the standardized phone call in English and will not be able to complete the informed consent.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:支持治疗
- 分配:非随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:using patient reminder systems before scheduled urodynamics studies
The study intervention will include all participating patients receiving a phone call from a study team member reading from a script before their scheduled appointment.
The phone call will involve consenting the patient for the study and a reminder to come in for the study with a comfortably full bladder, avoiding utilizing the lobby restroom before the appointment.
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Using patient reminder systems before scheduled urodynamics studies on patient satisfaction, preparedness, anxiety, and successful completion of the procedure to improve healthcare delivery by comparing a prospective intervention group with a historical control group.
|
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无干预:not using patient reminder systems before scheduled urodynamics studies
Participants for the historical control group will be identified through retrospective review of electronic medical records of patients who previously underwent scheduled urodynamics studies.
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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 |
|---|---|---|
|
Percent decrease in urodynamics procedure completion failure rate in patients who received the reminder system before scheduled urodynamics procedures vs. patients who did not receive the reminder
大体时间:From enrollment to the end of the urodynamics study (less than 1 week)
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Completion failure is defined as a uroflow less than 150 mL
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From enrollment to the end of the urodynamics study (less than 1 week)
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Evaluate anxiety before and after a urodynamics (UDS) procedure after delivery of a patient reminder system.
大体时间:From enrollment to the end of the urodynamics study (less than 1 week)
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Anxiety is measured by patient completion of ST-STAI before and after the UDS study.
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From enrollment to the end of the urodynamics study (less than 1 week)
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Evaluate patient satisfaction and preparedness before and after a urodynamic study after delivery of a patient reminder system.
大体时间:From enrollment to the end of the urodynamics study (less than 1 week)
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Patient satisfaction and preparedness for the procedure will be assessed using Likert-style items via a survey issued to patients before and after the UDS study.
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From enrollment to the end of the urodynamics study (less than 1 week)
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (估计的)
2026年8月1日
初级完成 (估计的)
2027年6月1日
研究完成 (估计的)
2027年12月1日
研究注册日期
首次提交
2026年7月2日
首先提交符合 QC 标准的
2026年7月2日
首次发布 (实际的)
2026年7月9日
研究记录更新
最后更新发布 (实际的)
2026年8月17日
上次提交的符合 QC 标准的更新
2026年8月13日
最后验证
2026年8月1日
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- STUDY20260760
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
不
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
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.