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NCT05633901 · ClinicalTrials.gov registry record · NA
Impact of Preop Video on Patient Anxiety
A NA study of Prolapse; Female and Prolapse, Vaginal, sponsored by TriHealth.
- Active
- Registry status
- NA
- Development phase
- 160
- Enrollment target
- 2
- Study locations
NCT05633901: Active NA study of Prolapse; Female and Prolapse, Vaginal, sponsored by TriHealth.
NCT05633901 is a NA study of Prolapse; Female and Prolapse, Vaginal that is active but no longer recruiting, run by TriHealth. The registered enrollment target is 160 participants, above the 109-participant average among 3 other Prolapse; Female trials with a reported enrollment target (47% higher). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05633901, a NA study of Prolapse; Female and Prolapse, Vaginal, is active but no longer recruiting, sponsored by TriHealth.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 160 participants
- Enrollment target
- 2
- Study locations
Study Summary
To determine whether a pre-operative educational video has an impact on the anxiety of patients undergoing vaginal prolapse surgery
Primary Outcome
Surgical Anxiety Questionnaire is a validated, 17 question survey with scores ranging from 0 (least anxious) to 68 (most anxious)
Conditions Studied
Interventions
- OTHER Educational Video
- OTHER Standard Counseling
Study Locations (2)
Ohio
- Cincinnati Urogynecology Associates - Cincinnati
- Good Samaritan Hospital - Cincinnati
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 160 participants |
| Start Date | 2022-12-07 |
| Est. Completion | 2024-12 |
| Phase | NA |
What the registry record for NCT05633901 still lists
NCT05633901 is an interventional study that assigns participants to a tested intervention. The registered 160 participants enrollment target is mid-sized for trials with a published cap, above the 109-participant average among 3 other Prolapse; Female trials with a reported enrollment target (47% higher).
The record links to 3 conditions, with Prolapse; Female appearing as the primary indexed condition, and to 2 interventions - of which Educational Video is the first listed.
NCT05633901 reports a single indexed study location in Ohio.
Frequently Asked Questions
What is clinical trial NCT05633901 about?
NCT05633901 is a clinical study titled "Impact of Preop Video on Patient Anxiety". To determine whether a pre-operative educational video has an impact on the anxiety of patients undergoing vaginal prolapse surgery
What is the current status of trial NCT05633901?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 160 participants. The study started on 2022-12-07. Estimated completion is 2024-12.
What conditions does trial NCT05633901 study?
This clinical trial studies the following conditions: Prolapse; Female, Prolapse, Vaginal, Prolapse, Uterine.
What interventions are being tested in trial NCT05633901?
The interventions under investigation include: Educational Video (OTHER), Standard Counseling (OTHER).
Who is sponsoring clinical trial NCT05633901?
This trial is sponsored by TriHealth, which has 81 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05633901 being conducted?
This trial has 2 study locations across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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