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

Recruiting now

Conditions studied: Levonorgestrel, Intrauterine Systems, Prevention, Endometrial Cancer

In brief

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 \[LNG-IUS\]).

Key facts

Study ID

NCT07382583

Run by

M.D. Anderson Cancer Center

People needed

270

Starts

2026-02-12

Expected to finish

2030-02-01

Last updated by the study team

2026-02-25

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• 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
• Must 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
• Healthcare Providers
• Physicians or advanced practice providers (physician assistants, nurse practitioners) from Family Medicine, Obstetrics \& Gynecology, Internal Medicine, or Endocrinology
• Must be at least 18 years old
• Must read and speak English or Spanish
• Must provide written, informed consent for qualitative interviews

You may not qualify if…

• N/A

Where it is running

• The Harris Health System (LBJ) — Houston, Texas, United States (enrolling)
• MD Anderson Cancer Center — Houston, Texas, United States (enrolling)

Full record on ClinicalTrials.gov

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