Improving Women's Function After Pelvic Radiation (NCT04544735) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Improving Women's Function After Pelvic Radiation
United States12 participantsStarted 2020-10-07
Plain-language summary
The purpose of the study is to develop and test an intervention combining physical therapy (PT) and coping skills training to improve women's sexual function after pelvic radiation.
Who can participate
Age range18 Years
SexFEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Cancer Survivors participating in the Intervention Development Interviews
Inclusion Criteria:
* Diagnosis of non-metastatic gynecologic (cervical, endometrial, vaginal, vulvar), anal, rectal, or bladder cancer
* Completed pelvic radiation treatment within the last 5 years
* 18 years of age or older
* Able to speak/read English
* Able to give meaningful informed consent
Exclusion Criteria:
* Major untreated or uncontrolled mental illness (e.g., schizophrenia)
* Unable to provide informed consent
Medical Providers Participating in Intervention Development Interviews
Eligibility Criteria:
* Oncology providers (e.g., radiation, medical, and surgical oncologists; nurses; advanced practice professionals) who provide care to women who receive pelvic radiation for gynecologic, anal, rectal or bladder cancers.
* Physical therapists with specialized certification in pelvic health or women's health physical therapy who provide care to patients in the outpatient setting.
Cancer Survivor User Testers
Inclusion Criteria:
* Diagnosis of non-metastatic gynecologic (cervical, endometrial, vaginal, vulvar), anal, rectal, or bladder cancer
* Completed pelvic radiation treatment in the past 2 to 24 months
* 18 years of age or older
* Able to speak/read English
* Able to give meaningful informed consent
Exclusion Criteria:
* Major untreated or uncontrolled mental illness (e.g., schizophrenia)
* Unable to provide informed consent
What they're measuring
1
Session Attendance
Timeframe: Following completion of the intervention, up to 12 months