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Recruiting NCT06089083

NCT06089083 PROmOting Gynecologic Cancer Patients With Frailty to Achieve Functional Recovery

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Clinical Trial Summary
NCT ID NCT06089083
Status Recruiting
Phase
Sponsor University of California, San Francisco
Condition Malignant Female Reproductive System Neoplasm
Study Type OBSERVATIONAL
Enrollment 500 participants
Start Date 2023-10-18
Primary Completion 2027-11-30

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Physical function assessmentSelf-reported Assessments and QuestionnairesSurgery (Standard of Care, Non-Interventional)

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 500 participants in total. It began in 2023-10-18 with a primary completion date of 2027-11-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study seeks to understand how frailty, a term that describes people who are more vulnerable stressors such as a new medical problem, affects the outcomes and quality of life in adult patients with gynecologic cancer.

Eligibility Criteria

Inclusion Criteria: * Age 18 years or greater * Undergoing evaluation for a newly diagnosed gynecologic malignancy * Ability of individual or legal guardian/representative to understand a written informed consent document, and the willingness to sign it Exclusion Criteria: * Contraindication to any study-related procedure or assessment * Does not speak a language for which the consent form and study materials are available

Contact & Investigator

Central Contact

Janet Titzler

✉ janet.titzler@ucsf.edu

📞 415-353-9600

Principal Investigator

Stephanie Cham, MD

PRINCIPAL INVESTIGATOR

University of California, San Francisco

Frequently Asked Questions

Who can join the NCT06089083 clinical trial?

This trial is open to female participants only, aged 18 Years or older, studying Malignant Female Reproductive System Neoplasm. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06089083 currently recruiting?

Yes, NCT06089083 is actively recruiting participants. Contact the research team at janet.titzler@ucsf.edu for enrollment information.

Where is the NCT06089083 trial being conducted?

This trial is being conducted at San Francisco, United States, Boston, United States.

Who is sponsoring the NCT06089083 clinical trial?

NCT06089083 is sponsored by University of California, San Francisco. The principal investigator is Stephanie Cham, MD at University of California, San Francisco. The trial plans to enroll 500 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology