跳至主要内容
临床试验/NCT07382583
NCT07382583
招募中
不适用

Development of a Shared Decision Tool to Facilitate Uptake of the Levonorgestrel-releasing Intrauterine System for the Primary Prevention of Endometrial Cancer

M.D. Anderson Cancer Center2 个研究点 分布在 1 个国家目标入组 270 人开始时间: 2026年2月12日最近更新:

概览

阶段
不适用
状态
招募中
入组人数
270
试验地点
2
主要终点
Patient Utility Questionnaire

概览

简要总结

To develop an educational tool to help patients and healthcare professionals make informed decisions about endometrial cancer and available prevention options for it (such as the use of a levonorgestrel-releasing intrauterine system [LNG-IUS]).

详细描述

Primary Objectives

The overall goal of this study is to create a personalized decision support educational tool for the use of LNG-IUS as a primary prevention strategy for women at risk of EC. The decision support tool will not replace the consultation with a clinician. Rather, it will help prepare the participant to better understand their options and prepare them for conversations with clinicians when making a decision about use of LNG-IUS. The primary objectives will be accomplished in two phases:

Phase 1 Primary Objective:

1. To identify decisional needs, participant values, and experiences for preferences regarding LNG-IUS through a mixed-methods approach

Phase 2 Primary Objective:

1. To develop and field-test a novel web-based SDM tool in English and Spanish incorporating a personalized EC risk calculator and focused on LNG-IUS as a primary prevention strategy

研究设计

研究类型
Observational
观察模型
Other
时间视角
Other

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

  • Unaffected women
  • Must be at least 18 years old
  • Must read and speak English or Spanish
  • Must be premenopausal
  • Must not have a prior history of EC or complex atypical hyperplasia
  • Must provide written, informed consent
  • No physical, psychological, or cognitive impairments that would preclude participation in an interview as determined by the PI or study team member
  • Affected women
  • Must be at least 18 years old
  • Must read and speak English or Spanish

排除标准

  • 未提供

研究组 & 干预措施

Phase 2

Develop and pilot test a web-based shared medical decision tool

干预措施: Survey using a questionnaire (Other)

Phase 1

Identify decisional needs, patient values and experiences

干预措施: Survey using a questionnaire (Other)

结局指标

主要结局

Patient Utility Questionnaire

时间窗: Through study completion; an average of 1 year

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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