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More info
You can access this
clinical trial
if you have
Satisfaction, Postoperative Complications or Pelvic Floor Disorder
and you are
over 18
years old
-
The phase for this study is not defined.
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The purpose

The OPTIONs study is a randomized controlled, non-inferiority study to evaluate postoperative care using outpatient clinic visits versus telephone calls for women undergoing surgery for pelvic floor disorders. The primary outcome is patient satisfaction using the Surgical-Consumer Assessment of Healthcare Providers and Systems (S-CAHPS) questionnaire provided by the Agency for Healthcare Research and Quality (AHRQ). Secondary outcomes include safety and cost analysis for patients' direct and indirect medical costs. Women who speak and understand either English or Spanish and planning to undergo an elective surgery for a pelvic disorder will be recruited. Baseline demographics, satisfaction, and cost analysis questionnaires will be acquired pre-operatively. Randomization will be assigned at the time of discharge from the hospital. Patients will either have scheduled clinic visits at 1-2 weeks, 6 weeks, and 3 months or telephone calls by a registered nurse at these same intervals. Questionnaires will be completed at 3 months for satisfaction and cost analysis.

Provided treatments

  • Behavioral: Telephone follow-up
  • Behavioral: Outpatient Clinic Visits

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT02891187. The sponsor of the trial is University of New Mexico and it is looking for 120 volunteers for the current phase.
Official trial title:
Outpatient Visits Versus Telephone Interviews for Postoperative Care: A Randomized Controlled Trial