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NCT07265973 · ClinicalTrials.gov registry record · NA
PREPARE: Perioperative REhabilitation Around Vaginal Prolapse RepAir Surgery for Recovery Enhancement
A NA study of Postoperative Physical Functioning, sponsored by University of New Mexi.
- Recruiting
- Registry status
- NA
- Development phase
- 92
- Enrollment target
- 1
- Study location
NCT07265973: Recruiting NA study of Postoperative Physical Functioning, sponsored by University of New Mexi.
NCT07265973 is a NA study of Postoperative Physical Functioning that is actively recruiting participants, run by University of New Mexi. The registered enrollment target is 92 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07265973, a NA study of Postoperative Physical Functioning, is actively recruiting participants, sponsored by University of New Mexi.
- RECRUITING
- Registry status
- NA
- Development phase
- 92 participants
- Enrollment target
- 1
- Study location
Study Summary
Pelvic organ prolapse is a common problem faced by millions of patients in the United States, leading to an estimated 200,000 surgeries per year. The majority of patients in the US undergoing vaginal suspension between the ages of 60-79. Deconditioning and decreased functional status after surgery can be more pronounced in elderly populations. It is important to explore ways to improve postoperative functioning for this vulnerable population. This research study is about how good your physical functioning is after surgery. The physical functioning we are studying consist of normal daily activities, such as walking up and down stairs. This study is for patients with pelvic organ prolapse who are getting vaginal surgery to correct the prolapse. By doing this study, we hope to learn more about ways to improve physical functioning after vaginal prolapse repair surgery. Patients will be chosen at random to participate in or not to participate in a home daily exercise program for 6 weeks. We have participants who do not participate in the home exercise program so that we can compare their physical functioning to the participants who do exercise at home. By doing this comparison, we can find out if the home exercise program helps postoperative physical functioning. If you are in the home exercise group, a possible benefit is to have better physical functioning after surgery. If you are not assigned to the exercise group, the benefit is being a part of a study that could potentially help other women and yourself in the future to have better physical functioning after surgery. Patients will be enrolled in teh study only if they are undergoing specific surgeries at the University of New Mexico to correct their pelvic organ prolapse.
Primary Outcome
Postoperative physical functioning will be assessed using a questionnaire. The specific questionnaire is the Patient Reported Outcomes Measurement Information Systems (PROMIS) Physical Function Short Form 20a.
Conditions Studied
Interventions
- OTHER Pelvic floor Home Exercise Program, this intervention is comprised of specific exercises that are easy to complete at home
Study Locations (1)
New Mexico
- University of New Mexico Hospital - Albuquerque
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 92 participants |
| Start Date | 2025-11-24 |
| Est. Completion | 2028-06-25 |
| Phase | NA |
What NCT07265973 shows while recruiting
NCT07265973 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 92 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower).
The record links to 1 condition, with Postoperative Physical Functioning appearing as the primary indexed condition, and to 1 intervention - of which Pelvic floor Home Exercise Program, this intervention is comprised of specific exercises that are easy to complete at home is the first listed.
NCT07265973 reports a single indexed study location in New Mexico.
Frequently Asked Questions
What is clinical trial NCT07265973 about?
NCT07265973 is a clinical study titled "PREPARE: Perioperative REhabilitation Around Vaginal Prolapse RepAir Surgery for Recovery Enhancement". Pelvic organ prolapse is a common problem faced by millions of patients in the United States, leading to an estimated 200,000 surgeries per year. The majority of patients in the US undergoing vaginal suspension between the ages of 60-79. Deconditioning and decreased functional status after surgery c...
What is the current status of trial NCT07265973?
This trial is currently recruiting. It is a NA study. The enrollment target is 92 participants. The study started on 2025-11-24. Estimated completion is 2028-06-25.
What conditions does trial NCT07265973 study?
This clinical trial studies the following conditions: Postoperative Physical Functioning.
What interventions are being tested in trial NCT07265973?
The interventions under investigation include: Pelvic floor Home Exercise Program, this intervention is comprised of specific exercises that are easy to complete at home (OTHER).
Who is sponsoring clinical trial NCT07265973?
This trial is sponsored by University of New Mexi, which has 76 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07265973 being conducted?
This trial has 1 study location across New Mexico. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT07265973's enrollment target sits among peer trials
92 938th of 2000 higher than 1,062 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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