跳至主要内容
临床试验/NCT04138810
NCT04138810已完成不适用

Assessment of Video-conference Technology for Post-operative Follow up in a Urogynecologic Population

University of Pennsylvania2 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2017年7月17日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
54
试验地点
2
主要终点
Patient Satisfaction Via the Patient Satisfaction Questionnaire -18

研究概览

简要总结

Postoperative follow up is necessary following any surgical procedure and has been conducted in the same manner since the field of surgery began. The study will determine feasibility and patient satisfaction of innovative postoperative virtual clinical encounters utilizing mobile video conference technology for women undergoing pelvic reconstructive surgery through a randomized controlled trial.

详细描述

This will be a prospective randomized control study comparing postoperative virtual clinical encounters versus traditional in-office postoperative visits in women undergoing pelvic reconstructive surgery. The postoperative experiences of both groups will be assessed via surveys. Virtual Clinical Encounter Group: - Receive video-conference call from office nurse 48-72 hours post discharge from hospital - Receive video-conference call from fellow and/or attending physician approximately 30 days (4-6 weeks) from surgery -- Complete telephone survey one day later - Have in-office postoperative visit with fellow and/or attending physician approximately 90 days (10-12 weeks) from surgery -- Fill out surveys after office visit Traditional Office Group: - Receive telephone call from office nurse 48-72 hours post discharge from hospital - Have in-office postoperative visit with fellow and/or attending physician approximately 30 days (4-6 weeks) from surgery -- Complete telephone survey one day later - Have in-office postoperative visit with fellow and/or attending physician approximately 90 days (10-12 weeks) from surgery -- Fill out surveys after office visit

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
Female
接受健康志愿者

入选标准

  • Undergoing surgery for pelvic organ prolapse
  • Age greater than 18
  • Access to a smartphone
  • Access to high speed internet access (via 4G or 3G on their smartphone or high speed Wi-Fi)
  • Signed up for MyPennMedicine web portal
  • Ability to download MyChart mobile application
  • Pennsylvania Hospital Subject: NJ or PA resident, HUP & Presbyterian Hospital Subject: PA resident

排除标准

  • Pregnancy
  • Inability to read, speak or understand English
  • Isolated midurethral sling procedure
  • Extraperitoneal vaginal colpopexy with Uphold mesh

结局指标

主要结局

Patient Satisfaction Via the Patient Satisfaction Questionnaire -18

时间窗: 30 days

PSQ-18 is a validated eighteen item patient satisfaction questionnaire that has been utilized across diverse healthcare settings. It measures satisfaction across the following domains: general satisfaction, technical quality of care, interpersonal manner of healthcare provider, communication, financial aspects of care, time spent with healthcare provider and accessibility/convenience of care. Total scores range from 18 to 90, with higher scores indicating higher patient satisfaction.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Daniel Lee

Principal Investigator

University of Pennsylvania

研究点 (2)

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