The Better, Harder, Faster, Stronger Study
Recruiting now
Conditions studied: Frailty at Older Adults, Ovarian Cancer, Endometrial Cancer, Cognitive Dysfunction, Neoadjuvant Chemotherapy
In brief
The purpose of this study is to evaluate changes in the electronic Frailty Index (eFI) score following 3-4 cycles of neoadjuvant chemotherapy (NACT) in participants with advanced ovarian and endometrial cancer.
Key facts
- Study ID
- NCT07220512
- Run by
- Wake Forest University Health Sciences
- People needed
- 35
- Starts
- 2025-07-28
- Expected to finish
- 2027-05-01
- Last updated by the study team
- 2026-07-15
Who can join
Age: 55 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Ability to understand and willingness to sign an IRB-approved informed consent.
- Age > 55 years at the time of enrollment.
- Newly diagnosed suspected ovarian/primary peritoneal/fallopian tube carcinoma of any histological subtype, FIGO Stage II-IV, per enrolling investigator, or newly diagnosed suspected endometrial carcinoma of any histologic subtype, FIGO Stage II-IV, per enrolling investigator.
- Planned for 3 or 4 cycles of NACT, with interval cytoreductive surgery planned thereafter.
- Ability to read, understand, and write the English language.
- As determined by the enrolling investigator, ability of the participant to understand and comply with study procedures for the entire length of the study.
You may not qualify if…
- History of brain metastases.
- History of poorly controlled psychiatric conditions, defined as hospitalization within the prior 3 months for psychiatric disorders, traumatic brain injury, cerebrovascular event, or dementia, per the enrolling investigator.
- Use of anti-amyloid agents, cholinesterase inhibitors, or Memantine for Alzheimers/cognitive impairment, at the time of enrollment.
- Vision impairment that would impede completion of study assessments, per enrolling investigator.
Where it is running
- Wake Forest Baptist Comprehensive Cancer Center — Winston-Salem, North Carolina, United States (enrolling)
Full record on ClinicalTrials.gov
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