[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT07692789":3,"trial-entities:NCT07692789":78,"trial-summary:NCT07692789":81},{"id":4,"nct_id":4,"org_study_id":5,"brief_title":6,"official_title":6,"overall_status":7,"completion_date":8,"status_verified_date":9,"last_update_date":10,"start_date":9,"sponsor_name":11,"lead_sponsor_class":12,"has_dmc":13,"brief_summary":14,"detailed_description":13,"conditions":15,"keywords":18,"study_type":19,"primary_purpose":20,"phases":21,"enrollment_info":23,"interventions":26,"primary_outcomes":32,"secondary_outcomes":37,"sex":44,"minimum_age":45,"maximum_age":13,"healthy_volunteers":46,"eligibility_criteria":47,"std_ages":51,"locations":54,"central_contacts":70,"overall_officials":75,"references":76,"see_also_links":77},"NCT07692789","STUDY20260760","Improving Uroflowmetry Interpretability: Evaluating the Impact of Patient Reminder Systems","RECRUITING","2027-12","2026-07","2026-07-31","Ohio State University","OTHER",null,"The purpose of this study is to evaluate the impact of pre-procedure patient reminder systems on patient satisfaction, preparedness, and anxiety among patients undergoing urodynamics studies. The rate of successful procedure completion will be compared between a prospective intervention group and a historical control group to determine whether the intervention improves procedural success and healthcare delivery.",[16,17],"Pelvic Organ Prolapse","Urinary Incontinence",[],"INTERVENTIONAL","SUPPORTIVE_CARE",[22],"NA",{"count":24,"type":25},162,"ESTIMATED",[27],{"type":12,"name":28,"description":29,"armGroupLabels":30},"Patient reminder system","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.",[31],"using patient reminder systems before scheduled urodynamics studies",[33],{"measure":34,"description":35,"timeFrame":36},"Percent decrease in urodynamics procedure completion failure rate in patients who received the reminder system before scheduled urodynamics procedures vs. patients who did not receive the reminder","Completion failure is defined as a uroflow less than 150 mL","From enrollment to the end of the urodynamics study (less than 1 week)",[38,41],{"measure":39,"description":40,"timeFrame":36},"Evaluate anxiety before and after a urodynamics (UDS) procedure after delivery of a patient reminder system.","Anxiety is measured by patient completion of ST-STAI before and after the UDS study.",{"measure":42,"description":43,"timeFrame":36},"Evaluate patient satisfaction and preparedness before and after a urodynamic study after delivery of a patient reminder system.","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.","FEMALE","18 Years",false,{"inclusion":48,"exclusion":49,"raw_text":50},[],[],"Inclusion Criteria\n\n1. Age 18 years or older\n2. Sex assigned at birth: Female.\n3. English-speaking\n4. Scheduled to undergo a urodynamics study at the OSU Upper Arlington Outpatient Clinic, OSU New Albany Outpatient Clinic, or OSU Eye and Ear Institute\n5. Ability to access a telephone\n6. Active MyChart account\n7. Ability to provide informed consent\n8. Documented post-residual volume of less than 150 mL\n9. Ability to be reached by telephone after three call attempts\n10. Negative point-of-care urinary tract infection on the day of the scheduled procedure (SOC)\n\nExclusion criteria:\n\n1. Under 18 years of age\n2. Patients with structural causes of urinary retention\u002Fincomplete bladder emptying (defined as a post-void residual \\>150ml) or a positive point-of-care urinary tract infection on the day of the procedure.\n3. Men are excluded as the population of interest is the female urogynecology population in both urology and obstetrics and gynecology.\n4. Patients without access to a telephone or an active MyChart account are excluded because the intervention relies on telephone calls and electronic messaging for delivery of pre-procedure education and reminders.\n5. Individuals who cannot be reached by telephone are excluded because they cannot receive the intervention.\n6. Non-English speaking individuals are excluded because they will not be able to receive the standardized phone call in English and will not be able to complete the informed consent.",[52,53],"ADULT","OLDER_ADULT",[55],{"facility":56,"status":7,"city":57,"state":58,"zip":59,"country":60,"contacts":61,"geoPoint":67},"Ohio State University Wexner Medical Center","Columbus","Ohio","43210","United States",[62],{"name":63,"role":64,"phone":65,"email":66},"Lisa Hickman, MD","CONTACT","614-814-8205","Lisa.Hickman@osumc.edu",{"lat":68,"lon":69},39.96118,-82.99879,[71,72],{"name":63,"role":64,"phone":65,"email":66},{"name":73,"role":64,"email":74},"Ashka Shah","Ashka.Shah@osumc.edu",[],[],[],{"nct_id":4,"conditions":79,"biomarkers":80},[16,17],[],{"nct_id":4,"found":82,"summary":83,"prompt_version":93},true,{"design":84,"status":85,"heading":86,"summary":87,"follow_up":88,"word_count":89,"commitments":90,"compensation":91,"drugs_mentioned":92},"This interventional study plans to enroll 162 women. It compares a group receiving a patient reminder system to a historical control group.","completed","Evaluating Patient Reminders for Urodynamics Studies","This study is looking at whether a patient reminder system can help improve how well urodynamics procedures (tests that check how your bladder and urethra are working) are completed. If you are a woman aged 18 or older, speak English, have a MyChart account, can use a phone, and are scheduled for a urodynamics study at one of the listed OSU clinics, you might be able to join. The researchers want to see if the reminder system reduces the number of failed procedures and also if it makes patients feel more satisfied, prepared, and less anxious. The study will compare patients who receive the reminder system to those who did not.","Your participation would involve the period from enrollment until the end of your urodynamics study, which is less than one week.",111,"You would receive a patient reminder system before your scheduled urodynamics study. The primary outcome is measured from enrollment to the end of the urodynamics study, which is less than one week.","Not stated in the trial record.",[28],"v2"]