Under construction – not a live service
Sign in
Taking people in United StatesNo phase

Coping and sexual health study for women with bladder cancer

Compares an education program with usual care for women with bladder cancer.

Plain-language title generated from the registry record
Registry title: Gender Related Coping and Survivorship for Genitourinary Cancers

Key facts

Where
Baltimore and Washington D.C., United StatesSee the 2 sites

Where in United States

  • Johns Hopkins HospitalBaltimore, United StatesTaking people
  • Sibley Memorial HospitalWashington D.C., United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Johns Hopkins University
Trial code
NCT05649306
Record updated
29 October 2026
Original description
This research is being done to learn more about coping and survivorship of women with bladder cancer, specifically regarding psychosocial distress and sexual dysfunction. This study is a non-therapeutic study and will randomize participants to a standard of care group and education group. Patients in both groups will be asked to complete surveys regarding their mood and sexual function. Patients in the intervention group will be asked to complete attendance diaries regarding educational and support services utilized. Participants' clinical data will also be collected.Read full original descriptionShow less

Gender Related Coping and Survivorship for Genitourinary Cancers

This research is being done to learn more about coping and survivorship of women with bladder cancer, specifically regarding psychosocial distress and sexual dysfunction. This study is a non-therapeutic study and will randomize participants to a standard of care group and education group. Patients in both groups will be asked to complete surveys regarding their mood and sexual function. Patients in the intervention group will be asked to complete attendance diaries regarding educational and support services utilized. Participants' clinical data will also be collected.

Inclusion: Females with bladder cancer; Willing to answer surveys regarding their psychosocial health and sexual health.

Exclusion: Not undergoing either active treatment or active surveillance (i.e. patients on hospice care); Patients with cognitive impairments; Women who are pregnant.

ClinicalTrials.gov NCT05649306