Helping gynecologic cancer patients discuss sexual health with their doctors
Promoting Effective Clinical Communication About Sexual Health After Gynecologic Cancer: A Randomized Controlled Trial of a Patient-Focused Intervention
This study tests if an educational video and workbook can help gynecologic cancer patients talk more openly about sexual health with their doctors and improve their overall well-being.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 200 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | Fox Chase Cancer Center Academic / other |
| Locations | 1 site (Philadelphia, Pennsylvania) |
| Trial ID | NCT06904339 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to determine if an educational video and workbook can enhance communication between gynecologic cancer patients and their healthcare providers regarding sexual health concerns. Participants will be divided into two groups: one receiving the educational program along with a resource booklet, and the other receiving only the resource booklet. The study will assess whether those who engage with the educational materials discuss sexual health issues more openly and experience improvements in sexual function, anxiety, and depression. Data will be collected through surveys and audio recordings of clinic visits.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older diagnosed with any stage of gynecologic cancer who are currently receiving treatment or have completed treatment within the last 10 years.
Not a fit: Patients who are unable to speak English or have significant cognitive or psychiatric issues may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could empower gynecologic cancer patients to address sexual health issues more effectively, leading to improved quality of life.
How similar studies have performed: While the specific approach of this study may be novel, similar educational interventions have shown promise in improving patient-provider communication in other healthcare contexts.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * At least 18 years old * Diagnosed with any stage (I-IV) gynecologic cancer * Receiving treatment for gynecologic cancer or completed active treatment less than 10 years ago * Attending visits in follow-up care at Fox Chase Cancer Center * Score of at least 3 on a sexual concerns screener question Exclusion Criteria: * Not able to speak English * Not willing to have clinic visit audio recorded * Eastern Cooperative Oncology Group (ECOG) score \> 2 * Overt cognitive dysfunction or psychiatric disturbance
Where this trial is running
Philadelphia, Pennsylvania
- Fox Chase Cancer Center — Philadelphia, Pennsylvania, United States (Recruiting)
Study contacts
- Study coordinator: Jennifer B Reese, PhD
- Email: jennifer.reese@fccc.edu
- Phone: 215-214-3223
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.