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NCT03890471 · ClinicalTrials.gov registry record · NA
Telephone Intervention to Increase Patient Preparedness and Satisfaction Trial (TIPPS): A Randomized Control Trial
A NA study of Stress Urinary Incontinence and Prolapse, sponsored by University of Texas at Austin.
- Completed
- Registry status
- NA
- Development phase
- 150
- Enrollment target
- 2
- Study locations
NCT03890471 is a NA study of Stress Urinary Incontinence and Prolapse that has completed, run by University of Texas at Austin. The registered enrollment target is 150 participants, roughly in line with the 158-participant average among 35 other Stress Urinary Incontinence trials with a reported enrollment target. The trial reports 2 study locations across 1 state.
The verdict
NCT03890471, a NA study of Stress Urinary Incontinence and Prolapse, has completed, sponsored by University of Texas at Austin.
- COMPLETED
- Registry status
- NA
- Development phase
- 150 participants
- Enrollment target
- 2
- Study locations
Study Summary
Surgical preparedness improves patient satisfaction and perioperative outcomes. In urogynecology, interventions to increase preoperative patient preparedness have not been adequately studied. Our objective is to evaluate the ability of preoperative provider-initiated telephone calls to increase patient preparedness for surgery. The investigators will conduct a randomized control trial comparing surgical preparedness between provider-initiated telephone call three days before surgery plus usual preoperative counseling versus usual preoperative counseling alone among women planning to undergo pelvic reconstructive surgery as measured by the Preoperative Patient Questionnaire (PPQ) and the Modified Preparedness for Colorectal Cancer Surgery Questionnaire (Modified PCSQ). Surgical satisfaction, perioperative outcomes, and medical costs will be also be compared between the two groups. Our hypothesis is that preoperative telephone calls will result in improved surgical preparedness. This novel approach in preoperative counseling has the potential to positively impact perioperative patient care. The investigators will also conduct an ancillary qualitative study of sexually active women undergoing pelvic reconstructive surgery who are enrolled in the randomized control trial. This work will aim to describe the patient experience, concerns, and the quality of the first sexual encounter following surgery. This ancillary study will lay the foundation for future investigations into how to better counsel patients and discuss sexual activity after surgical repair.
Conditions Studied
Interventions
- BEHAVIORAL Preoperative telephone call three days before surgery
Study Locations (2)
Texas
- Seton Midtown Medical Tower - Austin
- Pelvic Floor Integrated Practice Unit at the University of Texas Health Austin - Austin
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 150 participants |
| Start Date | 2019-06-05 |
| Est. Completion | 2020-05-11 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03890471
The ClinicalTrials.gov registry entry for NCT03890471 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 150 participants, a figure that helps gauge the scale of data the investigators plan to collect, roughly in line with the 158-participant average among 35 other Stress Urinary Incontinence trials with a reported enrollment target. The listed sponsor is University of Texas at Austin, which has 257 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Stress Urinary Incontinence appearing as the primary indexed condition, and to 1 intervention - of which Preoperative telephone call three days before surgery is the first listed.
NCT03890471 reports 2 study locations spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT03890471 about?
NCT03890471 is a clinical study titled "Telephone Intervention to Increase Patient Preparedness and Satisfaction Trial (TIPPS): A Randomized Control Trial". Surgical preparedness improves patient satisfaction and perioperative outcomes. In urogynecology, interventions to increase preoperative patient preparedness have not been adequately studied. Our objective is to evaluate the ability of preoperative provider-initiated telephone calls to increase pati...
What is the current status of trial NCT03890471?
This trial is currently completed. It is a NA study. The enrollment target is 150 participants. The study started on 2019-06-05. Estimated completion is 2020-05-11.
What conditions does trial NCT03890471 study?
This clinical trial studies the following conditions: Stress Urinary Incontinence, Prolapse.
What interventions are being tested in trial NCT03890471?
The interventions under investigation include: Preoperative telephone call three days before surgery (BEHAVIORAL).
Who is sponsoring clinical trial NCT03890471?
This trial is sponsored by University of Texas at Austin, which has 257 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03890471 being conducted?
This trial has 2 study locations across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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