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Pelvic Physical Therapy for Sexual Dysfunction in Gynecologic Oncology Survivors

StatusCompleted
PhaseNot applicable
Started
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Record History

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  1. Results posted: Sep 29, 2026 Show 4 more changesShow less
    • Primary and study completion dates: Sep 14, 2022 to Apr 10, 2023
    • Eligibility criteria expanded, about 9 words
    • Secondary endpoints: details revised at 2 of 2 entries
    • Study description expanded, about 2 words
  2. Primary and study completion dates: Nov 26, 2022 to Sep 14, 2022
    • Secondary endpoints: details revised at 2 of 2 entries
    • Eligibility criteria shortened, about 2 words
    • Collaborators expanded, about 4 words
    v8
  3. Re-verified, no change to tracked fieldsv7
  4. Trial status: Active, Not Recruiting to Completed
    • Study completion date changed from estimate of Nov 2023 to Nov 26, 2022
    v6
  5. Trial status: Recruiting to Active, Not Recruiting
    • Primary completion date changed from estimate of Jun 2023 to Nov 26, 2022
    • Study completion date: Jun 2023 to Nov 2023
    • Site details revised
    v5
Show 3 earlier versionsHide 3 earlier versions
  1. Re-verified, no change to tracked fieldsv4
  2. Start date changed from estimate of Mar 2022 to Mar 28, 2022v3
  3. Trial status: Not Yet Recruiting to Recruiting
    • Primary endpoints revised (3)
    • Study sites: 0 to 1
    • Start date: Apr 2022 to Mar 2022
    v2
  1. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The purpose of this research study is to investigate the use of pelvic physical therapy for gynecologic cancer survivors who report sexual dysfunction. Physical therapy experts believe that a full 10-week regimen is necessary for true improvement of symptoms. Investigators aim to see if this tense regimen is feasible for survivors. Investigators also aim to see if patients have an improvement in their sexual function and quality of life.
Trial Details
NCT Number NCT05242770
Lead Sponsor Wake Forest University Health Sciences
Collaborators: National Cancer Institute (NCI)
Conditions
(from sponsor)		 Gynecologic Cancer, Sexual Dysfunction
Related terms Sexual Dysfunction, Physiological
Enrollment 20 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov