A Study to Evaluate the Long-term Outcomes of a Comprehensive Pelvic Floor Rehabilitation Program

Overview

About this study

The purpose of this study is to evaluate long-term patient outcomes and satisfaction with our comprehensive pelvic floor rehabilitation program at 3-months, 6-months and 12-months following therapy completion.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

Patients referred for our pelvic floor rehabilitation program.
Patients with the following diagnosis will be offered participation in our study:
- urinary urgency or frequency;
- urinary incontinence (urgency, stress or mixed);
- defecatory dysfunction;
- fecal incontinence;
- pelvic pain;
- pelvic dysfunction (spasms, pain or weakness); or
- dyspareunia.

Exclusion Criteria:

Patients with implanted electrical devices.

Eligibility last updated 10/18/21. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location	Status	Contact
Rochester, Minn. Mayo Clinic principal investigator John Occhino, M.D., M.S.	Open for enrollment	Contact information: Darlene Vargas Maldonado M.D. VargasMaldonado.Darlene@mayo.edu

Mayo Clinic Location

Status

Contact

Rochester, Minn.

Mayo Clinic principal investigator

John Occhino, M.D., M.S.

Open for enrollment

Contact information:

Darlene Vargas Maldonado M.D.

VargasMaldonado.Darlene@mayo.edu

More information

Publications

Publications are currently not available

Clinical Trials