ClinicalTrials.gg
Enrolling by invitationNCT07910162Updated Nov 9, 2026

Developing a Gynecologic Cancer Health Promotion Community Engagement Program

An observational study in Gynecologic Cancer Survivors, sponsored by Abramson Cancer Center at Penn Medicine. Enrolling by invitation at 1 site in United States. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-11-09.

Sponsored by Abramson Cancer Center at Penn Medicine · Observational

Updated Nov 9, 2026Interventions changedNewly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
100
Ages
18 Years and older
Sex
Female
01

Study summary

The goal of this observational study is to learn about the communication systems of gynecologic cancer survivors by conducting focus groups and disseminating a survey.

Gynecologic cancer survivors at Penn Medicine who have consented to being contacted for participation in research will be asked to join the study.

Read the detailed description

First, a mixed-methods study of gynecologic cancer survivors will be conducted to assess perceptions, barriers, and facilitators to discussing gynecologic cancers through the family and community and create a toolkit for communication.

Separately, a network-map will be created to integrate social-community-advocacy-provider map to disseminate information and facilitate community-based participatory research in gynecologic cancers, by leveraging extensive collaborative teams locally and nationally.

02

Conditions studied

  • Gynecologic Cancer Survivors

Keywords

  • ovarian cancer survivor
  • endometrial cancer survivor
  • cervical cancer survivor
03

In context

Lead sponsor

Abramson Cancer Center at Penn Medicine is the lead sponsor of 460 studies on the registry; 87 are open to participants now.

Of its 33 completed or terminated interventional studies of FDA-regulated products, 14 (42%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Gynecologic cancer survivors at Penn Medicine who have consented to being contacted for participation in research

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Gynecologic cancer survivors at Penn Medicine who have consented to being contacted for participation in research.
  2. Age > 18 years old.
  3. Diagnosis of cancer at least 6 months prior to recruitment date.

Exclusion criteria

Exclusion Criteria:

  1. Age \< 18 years old.
  2. Patients unable to provide consent due to mental incapacity or lack of cognitive ability to understand the information provided.
  3. Diagnosis date within 6 months of recruitment date.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
100 participants (estimated)
Patient registry
No

Groups and cohorts

  • Ovarian cancer survivors

    Patients who have been diagnosed with ovarian cancer and have received at least 1 prior line of therapy.

  • Endometrial cancer survivors

    Patients who have been diagnosed with endometrial cancer and have received at least 1 prior line of therapy.

  • Cervical cancer survivors

    Patients who have been diagnosed with cervical cancer and have received at least 1 prior line of therapy.

06

What researchers measure

Primary outcomes

  1. Themes Identified from Focus Groups and Surveys

    Thematic analysis of transcripts from semi-structured interviews to identify primary thematic categories regarding barriers and facilitators to discussing gynecologic cancer. Count/listing of identified primary qualitative themes will be performed.

    Time frame: From enrollment to June 2027.

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Yes — Only IPD used in the results publication

No publications or documents are linked to this record.

09

Timeline

2 registry updates since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Jun 2026 (actual). Primary completion is estimated for Jun 2027, 12 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 17, 2026
First posted
Nov 2, 2026
StartActual
Jun 1, 2026
Primary completionEst.
Jun 1, 2027
CompletionEst.
Jun 1, 2028
Last update
Nov 9, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Interventions
Arm changed Ovarian cancer surivors→Ovarian cancer survivors
Nov 9, 2026
Registered
First appeared on the registry
Nov 2, 2026
Show all 2 updates
  1. Nov 9, 2026
    Interventions Arm changed Ovarian cancer surivors→Ovarian cancer survivors
    + 1 other change: verification date
  2. Nov 2, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07910162
Responsible party
Emily Ko, MD (Principal Investigator, Abramson Cancer Center at Penn Medicine) — Principal investigator
First posted
Nov 2, 2026
Start date
Jun 1, 2026
Primary completion
Jun 1, 2027 (estimated)
Completion
Jun 1, 2028 (estimated)
Last update
Nov 9, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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