跳至主要内容
临床试验/NCT07644819
NCT07644819尚未招募不适用

Reducing No-Shows in High-Risk Urology Patients Through Enhanced Preoperative Outreach

University of California, San Francisco1 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2026年8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
尚未招募
入组人数
68
试验地点
1

研究概览

简要总结

This study aims to evaluate the impact of reminder call intervention on no-shows for urologic procedures in patients identified to be high risk for no-showing. Patients scheduled to undergo a urologic procedure will be randomized into two groups: the intervention group, who receives a series of reminder calls and text messages about appointment details and patient questions prior to the procedure date; and the control group, who receives standard care only. Secondary outcomes include rates of patient re-scheduling and healthcare utilization.

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
All
接受健康志愿者

入选标准

  • Adults aged 18 years or older
  • Identified as high risk for no-show by the study predictive model
  • Scheduled to undergo a urologic procedure at UCSF/UCSF affiliated sites

排除标准

  • Younger than 18 years of age
  • Not scheduled for a urologic procedure

研究组 & 干预措施

Standard Care

No Intervention

Participants receive standard preoperative care, including procedure scheduling, preoperative anesthesia evaluation, and routine surgery center reminder calls.

Enhanced Preoperative Outreach

Experimental

Participants receive standard care plus reminder phone calls at 7 days, 3 days, 1 day, and the day of the procedure, text messaging access, assessment of barriers to attendance, and referral to social work when appropriate.

干预措施: Preoperative Outreach (Behavioral)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验