Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Malignant Female Reproductive System Neoplasm
  • Stage I Cervical Cancer AJCC v8
  • Stage I Uterine Corpus Cancer AJCC v8
  • Stage I Vaginal Cancer AJCC v8
  • Stage IIB Vaginal Cancer AJCC v8
  • Stage IB Vulvar Cancer AJCC v8
  • Stage IB1 Cervical Cancer AJCC v8
  • Stage II Cervical Cancer AJCC v8
  • Stage III Vaginal Cancer AJCC v8
  • Stage III Cervical Cancer AJCC v8
  • Stage IIIB Vulvar Cancer AJCC v8
  • Stage IIIC Uterine Corpus Cancer AJCC v8
  • Stage II Vulvar Cancer AJCC v8
  • Stage I Vulvar Cancer AJCC v8
  • Stage IA Cervical Cancer AJCC v8
  • Stage IA Uterine Corpus Cancer AJCC v8
  • Stage IIIA Cervical Cancer AJCC v8
  • Stage IVA Vaginal Cancer AJCC v8
  • Stage IA Vaginal Cancer AJCC v8
  • Stage IIIA Vulvar Cancer AJCC v8
  • Stage IIIB Cervical Cancer AJCC v8
  • Stage IIA2 Cervical Cancer AJCC v8
  • Stage IVA Uterine Corpus Cancer AJCC v8
  • Stage IIIB Uterine Corpus Cancer AJCC v8
  • Stage IB Uterine Corpus Cancer AJCC v8
  • Stage IA Vulvar Cancer AJCC v8
  • Stage IB Cervical Cancer AJCC v8
  • Stage IIA1 Cervical Cancer AJCC v8
  • Stage IIA Vaginal Cancer AJCC v8
  • Stage IIB Cervical Cancer AJCC v8
  • Stage III Uterine Corpus Cancer AJCC v8
  • Stage II Vaginal Cancer AJCC v8
  • Stage IIA Cervical Cancer AJCC v8
  • Stage IB Vaginal Cancer AJCC v8
  • Stage IA1 Cervical Cancer AJCC v8
  • Stage IB2 Cervical Cancer AJCC v8
  • Stage IIIC2 Uterine Corpus Cancer AJCC v8
  • Stage IVA Cervical Cancer AJCC v8
  • Stage II Uterine Corpus Cancer AJCC v8
  • Stage IIIC1 Uterine Corpus Cancer AJCC v8
  • Stage IA2 Cervical Cancer AJCC v8
  • Stage IIIA Uterine Corpus Cancer AJCC v8
  • Stage IVA Vulvar Cancer AJCC v8
  • Stage IIIC Vulvar Cancer AJCC v8
  • Stage III Vulvar Cancer AJCC v8
Type
Interventional
Phase
Not Applicable
Design
Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Supportive Care

Participation Requirements

Age
Younger than 125 years
Gender
Only males

Description

PRIMARY OBJECTIVE: I. To determine the feasibility of a sexual health counseling intervention before and after pelvic radiation for women with gynecologic cancers. SECONDARY OBJECTIVE: I. To preliminarily evaluate the efficacy of a sexual health counseling intervention on patient reported outcomes i...

PRIMARY OBJECTIVE: I. To determine the feasibility of a sexual health counseling intervention before and after pelvic radiation for women with gynecologic cancers. SECONDARY OBJECTIVE: I. To preliminarily evaluate the efficacy of a sexual health counseling intervention on patient reported outcomes in quality of life, sexual function, and genitourinary symptoms. OUTLINE: Patients receive sexual health counseling prior to starting and at the completion of radiation. After completion of study, patients are followed up at 1 and 6 months after radiation.

Tracking Information

NCT #
NCT04269837
Collaborators
National Cancer Institute (NCI)
Investigators
Principal Investigator: Allison M Quick, MD Ohio State University Comprehensive Cancer Center