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NCT04204811Active, not recruiting

Prehabilitation Care for Women With Advanced Ovarian Cancer Receiving Neoadjuvant Chemotherapy

A Pilot Project to Evaluate Feasibility and Patient Experience of Prehabilitation Care for Women With Advanced Ovarian Cancer Undergoing Neoadjuvant Chemotherapy

Source: ClinicalTrials.gov · Last updated 7 Jan 2026

Brief summary (registry, in English)

The purpose of this study is evaluate whether a prehabilitation program is feasible and useful for women with advanced ovarian cancer receiving chemotherapy in preparation for debulking surgery.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
22 (estimated)
First submitted
17 Dec 2019
Start date
16 Dec 2019
Primary completion date
16 Dec 2026
Lead sponsor
Memorial Sloan Kettering Cancer Center
NCT number
NCT04204811

What you commit to

  • Study type: Interventional
  • Planned participants: 22
  • From 16 Dec 2019 to the primary completion date, 16 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior treatment for ovarian cancer
  • Immediate surgery plan without neoadjuvant treatment
  • No intended surgical plan
  • Chemotherapy administration exclusively planned at MSKCC regional site

Age

  • Patient under age 18

Other

  • Second opinion visit only
  • Patient unwilling to sign consent

Who the study is looking for

  • Subjects must be diagnosed with Stage III or Stage IV ovarian carcinoma (which includes primary peritoneal carcinoma or fallopian rube carcinoma)
  • All subjects must be enrolled within 90 days of diagnosis
  • No prior treatment for ovarian carcinoma
  • All subjects have agreed to a treatment plan of neoadjuvant chemotherapy and subsequent planned interval debulking surgery with an MSKCC surgeon
  • Participants must be initiating treatment at Gynecologic Medical Oncology clinics at MSKCC Manhattan
  • Proficiency in English in the determination of the investigators of by patient self-report

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Memorial Sloan-Kettering Cancer Center
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.