跳至主要内容
临床试验/NCT03809468
NCT03809468已完成不适用

Patient Satisfaction With Initial Phone Call Versus Office Visit Following Minimally Invasive Hysterectomy, a Randomized Controlled Trial.

The Cleveland Clinic2 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2019年1月16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
68
试验地点
2
主要终点
patient satisfaction

研究概览

简要总结

Patients will be randomized to clinic or telephone follow up after outpatient TLH. surveys will document patient satisfaction.

详细描述

This is a randomized controlled trial looking at patient satisfaction with a 1-2 week postoperative visit versus phone call after minimally invasive hysterectomy. Patients will be screened, enrolled, consented, and randomized during the preoperative office encounter, which usually takes place 30 days prior to their scheduled surgery. Patients randomized to the study group (1-2 week postoperative phone call) will be given a time and date when to expect the postoperative phone call. Patients randomized to the control arm will receive a standard postoperative visit appointment 7-21 days after surgery. Patients in both arms will receive postoperative discharge instructions advising when to contact our office and when to present to the emergency room with certain complaints. The patients in the study arm will have instructions reinforcing that they will be contacted with a postoperative phone call instead of a visit initially; however, patients in both arms will have a postoperative visit 6-8 weeks following surgery.

After surgery, patients randomized to the study arm will receive the phone call at 7-14 days post-op. The physician performing the phone call will be a minimally invasive gynecology fellow in our practice. The provider will use a script to review all of the typical review of systems and pertinent postoperative functioning questions typically reviewed and documented in our postoperative visit. They will also review the surgical pathology at this time. This conversation will be documented in our electronic medical record.

Patients randomized to the control arm will undergo typical office visit at 7-21 days postop.

Patients in both arms will have postoperative office visits at 6-8 weeks postop, and will complete a survey at that time. The survey is a modified version of the SCAHPS survey to assess patient satisfaction with the surgical experience. There will also be some questions about the patients' attitudes towards the number and timing of postoperative visits.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

性别
Female
接受健康志愿者

入选标准

  • women undergoing minimally invasive hysterectomy

排除标准

  • patients without adequate phone or transportation access
  • patients with concern for underlying malignancy

结局指标

主要结局

patient satisfaction

时间窗: 6-8 weeks postop

patient satisfaction scores

次要结局

  • phone calls and visits (unplanned)(6-8 weeks postop)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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