eSense-Cancer: Adapting an Online Intervention for Sexual Health Concerns to Gynecologic Cancer (NCT06619769)
🩺 Plain-English Summary (8th-Grade Level)
Sexual health is a vital component of gynecologic cancer treatment and survivorship. Unfortunately, most gynecologic cancer survivors lack sufficient information about the impact of cancer on sexual health and treatment opportunities. This research aims to assess how well an adapted online health intervention meets the sexual health needs of gynecologic cancer survivors and to test the efficacy of the new platform. If successful, eSense-Cancer may increase access to treatment for gynecologic cancer survivors, including those living in remote areas or facing other accessibility barriers. It may also fill healthcare gaps for survivors of varying ethnicity, sexual orientation, socioeconomic status, and gender.
Who can join: Review the eligibility criteria below.
Location: University of British Columbia — Vancouver, British Columbia
Age range: 19 Years
🧪 Interventions in This Study
- eSense-Cancer CBT: an online cognitive-behavioural therapy based intervention for sexual health concerns after gynecologic cancer (BEHAVIORAL)
- Navigator support for eSense-Cancer (BEHAVIORAL)
- Behavioral: eSense-Cancer MBT: an online cognitive-behavioural therapy based intervention for sexual health concerns after gynecologic cancer (BEHAVIORAL)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (1 Sites)
- University of British Columbia — Vancouver, British Columbia
📞 Contact the Study Coordinator
Phone: (604) 875-4111
Email: nisha.marshall@cw.bc.ca
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Gynecologic Cancers
- Pelvic Health Rehabilitation After Breast and Gynecologic Cancer — Edmonton, Alberta
- A Study to Assess Change in Disease Activity and Adverse Events in Adult Participants With Gynecologic Cancers Receiving Intravenous Infusion of IMGN151 as Monotherapy or in Combination With Other Therapies — Teaneck, New Jersey
- Communication About Sexual Health in Gynecologic Cancer — Philadelphia, Pennsylvania
- A Prospective Study of a Lifestyle Medicine Survivorship Program for Patients With Gynecologic Cancer — Orlando, Florida
- Virtual Mindful After Cancer (MAC) Intervention to Promote Sexual Health for Breast and Gynecologic Cancer Survivors — Corvallis, Oregon
Explore by condition: All Gynecologic Cancers clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.