Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT05752448

Survivorship Care for Women Living With Ovarian Cancer: (POSTCARE-O)

Led by Baylor College of Medicine · Updated on 2026-04-03

120

Participants Needed

3

Research Sites

184 weeks

Total Duration

On this page

Sponsors

B

Baylor College of Medicine

Lead Sponsor

C

Cancer Prevention Research Institute of Texas

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study will enroll 120 women living with ovarian cancer following completion of initial treatment. Our objective is to test an intervention designed to provide support during the survivorship transition for this population, who live with a high degree of morbidity related to the illness and its treatment as well as a high risk of recurrence. Study participants will be randomly assigned to receive survivorship care using the POSTCare-O process or usual care. The primary outcome is quality of life at 12 weeks after intervention.

CONDITIONS

Official Title

Survivorship Care for Women Living With Ovarian Cancer: (POSTCARE-O)

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women with stage 2 to 4 ovarian cancer
  • Treated with some combination of surgery, chemotherapy, biologics, or maintenance therapy
  • Within 6 months of completing initial ovarian cancer treatment (continued maintenance therapy allowed)
  • Able to provide consent in English or Spanish
Not Eligible

You will not qualify if you...

  • Admission to hospice care at the completion of ovarian cancer treatment

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Trial Site Locations

Total: 3 locations

1

UT Southwestern Parkland Health and Hospital System

Dallas, Texas, United States, 75235

Not Yet Recruiting

2

Dan L Duncan Comprehensive Cancer Center at the O'Quinn Medical Tower at Baylor St. Luke's Medical Center

Houston, Texas, United States, 77030

Actively Recruiting

3

Harris Health Smith Clinic

Houston, Texas, United States, 77054

Actively Recruiting

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Research Team

N

Nimrah Saleem, MPH

CONTACT

J

Judy Bettencourt, MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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