Recruiting

Home Exercise Program

Sponsor:

University of New Mexico

Code:

NCT07265973

Conditions

Postoperative Physical Functioning

Eligibility Criteria

Sex: Female

Age: 18+

Healthy Volunteers: Accepted

Interventions

Pelvic floor Home Exercise Program, this intervention is comprised of specific exercises that are easy to complete at home

Study Details

Brief 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.

Conditions

Postoperative Physical Functioning

Study ID

NCT07265973

Start date

Nov 24, 2025

Status verified date

Aug, 2026

Completion date

Jun 25, 2028

Anticipated

Primary completion date

Jun 25, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: Female

Age: 18+

Healthy Volunteers: Accepted

Inclusion Criteria:

  • Subjects are ≥ 18 years of age
  • English or Spanish speaking
  • Stage 2, 3 or 4 uterovaginal or vaginal vault prolapse.
  • Patient scheduled to undergo transvaginal sacrospinous ligament suspension, uterosacral ligament suspension, or Manchester procedure at The University of New Mexico Hospital.

Exclusion Criteria:

  • Inability to speak English or Spanish
  • Currently enrolled in Pelvic floor physical therapy
  • Inability to perform the home exercises
  • Dementia
  • Inability to fill out questionnaires
  • Inability to access video via internet
  • Undergoing concomitant surgeries that involve: InterStim, bladder hydrodistension/fulguration, pelvic floor Botox, mesh excision/complications.

Study Design

Enrollment

56 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Other

Interventions and Outcome Measures

Arms

no intervention: Routine Perioperative Care

This arm consists of control subjects who are not assigned to an intervention

experimental: Home Exercise Program

This arm consists of subjects who are assigned to perform the home exercise intervention

Interventions

Pelvic floor Home Exercise Program, this intervention is comprised of specific exercises that are easy to complete at home

Many exercise regimens focus on strengthening your pelvic floor. The intervention for this study is a novel pelvic floor physical therapy program that focuses on relaxing, stretching, and protecting the pelvic floor.

Primary outcome measure

  • Postoperative physical functioning [ Time Frame: Physical functioning will be assessed at baseline when patint is enrolled. Physical functioning will also be assessed postoperatively at 1, 2, and 6 weeks after surgery. ]

Central Contacts and Locations

Central contacts

Karen Clinical Reseach Manager

505-272-7541kataylor@salud.unm.edu

Locations

University of New Mexico Hospital

Recruiting

Albuquerque, New Mexico, United States, 87106

More Information

Sponsor

University of New Mexico

Last update posted

Aug 6, 2026

Last verified

Aug, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of New Mexico on 2026-08-06.