跳至主要内容
临床试验/NCT06975033
NCT06975033招募中不适用

The Impact of Discharge Educational Discharge Videos on Post-Operative Care Utilization After Holmium Laser Enucleation of the Prostate (HoLEP) Procedures

University of California, San Francisco3 个研究点 分布在 1 个国家目标入组 114 人开始时间: 2025年11月4日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
114
试验地点
3
主要终点
Number of Post-operative Healthcare Utilization Events

研究概览

简要总结

This will be a randomized interventional study. Patients scheduled to undergo a HoLEP at UCSF will be randomized into two groups after the procedure: one group will watch a scripted educational HoLEP video and the other group will not receive a video. We will monitor the post-operative care utilization after discharge. Secondary outcomes will include patient satisfaction.

研究设计

研究类型
Interventional
分配方式
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 —(Adult, Older Adult)
性别
Male
接受健康志愿者
否

入选标准

  • •Adults aged 18+
  • •Patients scheduled for a HoLEP procedure
  • •Patients willing to complete both baseline and follow up surveys
  • •Patients able to provide informed consent
  • •Patients are English-speaking and understand English

排除标准

  • •Patients under 18+
  • •Patients unable to consent
  • •Patients unable to complete surveys
  • •Patients without a prostate.
  • •Patients are non-English speakers

研究组 & 干预措施

Video

Experimental

Participants will watch video.

干预措施: Video (Other)

No Video

No Intervention

Participants will not watch video.

结局指标

主要结局

Number of Post-operative Healthcare Utilization Events

时间窗: up to 90 days (estimated time frame between initial surgery and first follow up visit)

Healthcare utilization will include MyChart messages, phone calls to clinic, unscheduled clinic visits, hospital readmissions, and emergency/urgent care visits.

Participant Satisfaction Score

时间窗: up to 90 days (estimated time frame between initial surgery and first follow up visit)

Measured using Likert scale survey ranging from 1 (strongly agree) to 5 (strongly disagree).

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor
主要研究者

David Bayne, MD, MPH

Principal Investigator - Physician

University of California, San Francisco

研究点 (3)

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