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Effects of a Follow-up Based Nursing Care Protocol on Pelvic Organ Prolapse

StatusCompleted
PhaseNot applicable
Started
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Record History

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  1. Primary endpoint(s) modified Show 12 more changesShow less
    • Completed without a posted recruiting period
    • Interventions modified
    • Trial arms changed: 6 → 2
    • Enrollment target: estimated 102 to confirmed 106
    • Study completion date changed from estimate of Dec 31, 2025 to Jan 15, 2026
    • Start date changed from estimate of Mar 1, 2025 to Oct 1, 2023
    • Eligibility criteria expanded, about 6 words
    • Secondary endpoints: 5 to 3
    • Study description shortened, about 68 words
    • Site details revised
    • Publications: details revised at 10 of 10 entries
    • Study title expanded, about 4 words
  2. Primary completion date: Dec 15, 2024 to Oct 15, 2025
    • Start date: Nov 1, 2024 to Mar 1, 2025
    • Study completion date: Dec 15, 2024 to Dec 31, 2025
    v2
  3. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 goal of this clinical trial is to evaluate the effects of a follow-up-based nursing care protocol-implemented during the perioperative and post-discharge home care processes-on pelvic organ prolapse symptoms, quality of life, and sexual functions in women who underwent surgery for pelvic organ prolapse. The main questions it aims to answer are: Is the follow-up-based nursing care protocol effective in reducing pelvic organ prolapse symptoms and improving quality of life and sexual functions? What are the comparative outcomes between the intervention group (receiving video-supported education and structured follow-ups at 2 weeks, 6 weeks, 3 months, and 6 months) and the control group (receiving routine perioperative nursing care)? Researchers will compare the intervention and control groups to determine the impact of the nursing care protocol on patients' recovery, quality of life, and symptom scores over a 6-month period.
Trial Details
NCT Number NCT06631508
Lead Sponsor Saglik Bilimleri Universitesi
Conditions
(from sponsor)		 Pelvic Organ Prolapse
Related terms Pelvic Organ Prolapse
Enrollment 106 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov