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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 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. The trial reports 1 study location across 1 state.

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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.

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

FieldValue
Enrollment Target 92 participants
Start Date 2025-11-24
Est. Completion 2028-06-25
Phase NA

Sponsor

University of New Mexi

76 total trials

What the Registry Record Tells You About NCT07265973

The ClinicalTrials.gov registry entry for NCT07265973 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 92 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of New Mexi, which has 76 total studies on file at ClinicalTrials.gov.

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 1 study location spanning 1 distinct geographic area - top geographies include 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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

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