Operations and pelvic muscle training in the management of apical support loss (OPTIMAL) trial: Design and methods

DOI

10.1016/j.cct.2008.12.001

Document Type

Journal Article

Publication Date

3-1-2009

Publication Title

Contemporary Clinical Trials

Volume

30

Issue

2

First Page

178

Last Page

189

ISSN

15517144

Keywords

Behavioral therapy, Factorial design, Pelvic floor muscle training, Pelvic organ prolapse, Randomized surgical trial, Sacrospinous ligament fixation, Stress urinary incontinence, Uterine prolapse, Uterosacral ligament suspension, Vaginal prolapse

Abstract

The primary aims of this trial are: 1) to compare surgical outcomes following sacrospinous ligament fixation to uterosacral vaginal vault suspension in women undergoing vaginal surgery for apical or uterine pelvic organ prolapse and stress urinary incontinence and 2) to examine the effects of a structured perioperative program consisting of behavioral techniques and pelvic floor muscle training compared to usual care. This trial is performed through the Pelvic Floor Disorders Network (PFDN), which is funded by National Institute of Child Health and Human Development. Subjects will be enrolled from hospitals associated with seven PFDN clinical centers across the United States. A centralized biostatistical coordinating center will oversee data collection and analysis. Two approaches will be investigated simultaneously using a 2 × 2 randomized factorial design: a surgical intervention (sacrospinous ligament fixation versus uterosacral vaginal vault suspension) and a perioperative behavioral intervention (behavioral and pelvic floor muscle training versus usual care). Surgeons have standardized essential components of each surgical procedure and have met specific standards of expertise. Providers of the behavioral intervention have undergone standardized training. Anatomic, functional, and health-related quality of life outcomes will be assessed using validated measures by researchers blinded to all randomization assignments. Cost-effectiveness analysis will be performed using prospectively collected data on health care costs and resource utilization. The primary surgical endpoint is a composite outcome defined by anatomic recurrence, recurrence of bothersome vaginal prolapse symptoms and/or retreatment and will be assessed 2 years after the index surgery. Endpoints for the behavioral intervention include both short-term (6-month) improvement in urinary symptoms and long-term (2-year) improvement in anatomic outcomes and prolapse symptoms. This article describes the rationale and design of this randomized trial, focusing on several key design features of potential interest to researchers in the field of female pelvic floor disorders and others conducting randomized surgical trials. © 2008 Elsevier Inc. All rights reserved.

Open Access

Green Accepted

Link to Full Text

Share

COinS