20
Participants
Start Date
March 28, 2022
Primary Completion Date
November 26, 2022
Study Completion Date
November 26, 2022
Control Arm
Participants randomized to this arm will only receive educational pamphlets with resources for sexual dysfunction and will not participate in physical therapy. Participants will be contacted at 3 months and 6 months to fill out two questionnaires about sexual function and quality of life. After 6months, if participants desire a referral to physical therapy, investigators will provide a referral.
Physical Therapy Arm
Participants will receive a referral to begin a pelvic physical therapy regimen. Participants will complete the sexual function and quality of life questionnaires after completion of the physical therapy regimen and again 3 months after. There will be a brief exit interview.
European Organization for the Research and Treatment of Cancer Quality of Life Questionnaire (EORTC-QLQ-C30)
Questionnaire designed to measure cancer patients' physical, psychological and social functions
Female Sexual Function Index (FSFI)
19-item self-report inventory designed to assess female sexual function.
Exit Interview
11-item questionnaire for participants to give feedback to investigators about teir experience with the intervention.
Wake Forest Baptist Comprehensive Cancer Center, Winston-Salem
Wake Forest University Health Sciences
OTHER