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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 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.

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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

Interventions

  • OTHER Educational Video
  • OTHER Standard Counseling

Study Locations (2)

Ohio

  • Cincinnati Urogynecology Associates - Cincinnati
  • Good Samaritan Hospital - Cincinnati

Trial Details

FieldValue
Enrollment Target 160 participants
Start Date 2022-12-07
Est. Completion 2024-12
Phase NA

Sponsor

TriHealth

81 total trials

What the Registry Record Tells You About NCT05633901

The ClinicalTrials.gov registry entry for NCT05633901 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 160 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 109-participant average among 3 other Prolapse; Female trials with a reported enrollment target (47% higher). The listed sponsor is TriHealth, which has 81 total studies on file at ClinicalTrials.gov.

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 2 study locations spanning 1 distinct geographic area - top geographies include 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.

Similar trials for Prolapse; Female

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.