New nurse-led program to support women with early menopause after cancer
Official title: Improving Outcomes for Women Experiencing Premature or Early Menopause After Cancer: Development and Pilot Testing of a Novel Intervention
Run by Duke University · NCT06982677 · Data updated 2026-11-12
A nurse navigator–led program is being tested to see if it helps women who have early or premature menopause after cancer feel more knowledgeable, confident, and better at managing symptoms.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 44 Years |
| Sex | Women only |
| Enrollment | 117 (estimated) |
| Sponsor | Duke University Academic / other |
| Locations | 1 site (Durham, North Carolina) |
| Status | Recruiting |
| Started | January 20, 2026 |
| Main results expected | May 2027 |
| Study ends | May 2027 |
| Registry record updated | May 14, 2026 |
| Trial ID | NCT06982677 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are women aged 18–44 who completed most cancer treatment (not including endocrine therapy) and have been amenorrheic for 12+ months.
✕Probably not a fit
Patients who are not experiencing or seeking help with menopause-related symptoms or who do not engage with virtual sessions may see limited benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This project develops and tests a nurse navigator–delivered intervention for women who experience premature or early menopause following cancer treatment. It follows a two-phase approach: first refining the program with input from survivors and clinicians, then piloting a randomized trial to assess feasibility and acceptability. Participants are randomized to receive the nurse navigator program or an educational control via video sessions and complete assessments at baseline and about 10 weeks later. The study emphasizes personalized education, decision support, self-efficacy, and cognitive-behavioral strategies for symptom management.
Why it matters
Potential benefit: If successful, the program could improve knowledge, decision-making, confidence, and symptom management for patients facing early menopause after cancer.
How similar studies have gone: Previous work on nurse-led, patient-activation–based interventions suggests potential benefits for symptom management, though this exact approach is novel in this specific population.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * female (biological sex); * 18 to 44 years old; * completed cancer treatment (other than endocrine therapy) \>12 months prior to enrollment; * have not had a period for more than 12 months (amenorrhea); * able to speak and read English. Exclusion Criteria: * diagnosis of metastatic cancer; * visual or hearing impairment that would interfere with participation in study; * cognitive impairment or severe mental illness that would interfere with participation in study.
Where it's running
-
Duke Cancer Institute
Durham, North Carolina, United States Recruiting
Study contacts
- Principal investigator: Rebecca Shelby, PhD — Duke University
- Study coordinator: Smrithi Divakaran, MPH
- Email: smrithi.divakaran@duke.edu
- Phone: 919-681-7695
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.