Ohio State University Wexner Medical Center
Columbus, Ohio, 43210, United States
NCT Number: NCT07692789
The purpose of this study is to compare the rate of successful urodynamics procedure completion between a prospective intervention group and a historical control group after a pre-procedure patient reminder system to determine whether the intervention improves procedural success and healthcare delivery. The impact of the reminder system on patient satisfaction, preparedness, and anxiety will also be evaluated.
Trial opening soon.
Get Notified18 year and older
Female
Interventional
Not applicable
Columbus, Ohio, 43210, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Using patient reminder systems before scheduled urodynamics studies on patient satisfaction, preparedness, anxiety, and successful completion of the procedure to improve healthcare delivery by comparing a prospective intervention group with a historical control group.
Time frame: From enrollment to the end of the urodynamics study (less than 1 week)
Completion failure is defined as a uroflow less than 150 mL
Time frame: From enrollment to the end of the urodynamics study (less than 1 week)
Anxiety is measured by patient completion of ST-STAI before and after the UDS study.
Time frame: From enrollment to the end of the urodynamics study (less than 1 week)
Patient satisfaction and preparedness for the procedure will be assessed using Likert-style items via a survey issued to patients before and after the UDS study.
Contact information is provided by the study sponsor or research team.
Ohio State University
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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