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NCT07091565Enrolling by invitation

Supporting Sexual Recovery in Women With Bladder Cancer

SPARC: Supporting Sexual Recovery in Women With Bladder Cancer

Source: ClinicalTrials.gov · Last updated 3 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This study looks at how bladder cancer and removing the bladder can affect women's sexual well-being. Bladder cancer can be more serious in women, and treatment like bladder removal can impact how they feel about themselves and their relationships. Women who've gone through this say it's important to talk about and get support for their sexual recovery. The study has three main parts. First, it reviews what is already known. Next, it involves talking to women with bladder cancer and the doctors and nurses who care for them. Finally, the team will use what they learn to create a toolkit to help healthcare workers support women's sexual recovery. Women with bladder cancer are helping to design this study. Their input shapes the questions and tools. The final toolkit will include training for doctors and nurses and be shared online and through charities. The aim is to make this part of regular healthcare.

Status (registry)
Enrolling by invitation
Study type
Observational
Enrollment
60 (estimated)
First submitted
21 Jul 2025
Start date
1 Aug 2025
Primary completion date
Jun 2026
Lead sponsor
King's College London
NCT number
NCT07091565

What you commit to

  • Study type: Observational
  • Planned participants: 60
  • From 1 Aug 2025 to the primary completion date, Jun 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Criteria the registry did not label

  • Patient Inclusion
  • All women and other patients with a clitoris, vagina, neo-vagina or neo-clitoris
  • Have a diagnosis of BCa-any grade/stage and have had a cystectomy (bladder removal)
  • At least 6 months after cystectomy
  • \>/ 18 years old
  • Written informed consent.
    • HCP Inclusion
  • All those working directly within a bladder cancer speciality
  • Professional registration
  • Written informed consent
    • Patient Exclusion
  • Poor command of the English language to the extent that the researcher judges this to critically undermine the ability to achieve the objectives of the interview.
  • A judgement by the researcher or the individual's clinician, based on either clinical appraisal (capacity assessment) or review of the individual's medical notes, that the individual has a cognitive functioning impairment that would interfere with ability to understand and complete the interview.
  • Documentation in the accessible medical notes of a psychiatric condition that would hamper participation in interview.
  • A judgement by the researcher or the individual's clinician, based on either clinical appraisal or review of the individual's medical notes, that the individual is too ill to participate; or is ill enough that participation would produce an unreasonable burden on that individual.
  • Aged \<18 years.
    • HCP Exclusion:
    • -Those without professional registration

Age in the registry: 18 years to - · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
King's College London
Coordinator of this site? Confirm its status
LondonUnited KingdomUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.