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NCT02313701 · ClinicalTrials.gov registry record · NA
Effect of Standardized Consent for Urogynecological Procedures on Patient Satisfaction
A NA study, sponsored by Beth Israel Deaconess Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 64
- Enrollment target
NCT02313701 is a NA study that has completed, run by Beth Israel Deaconess Medical Center. The registered enrollment target is 64 participants.
The verdict
NCT02313701, a NA study, has completed, sponsored by Beth Israel Deaconess Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 64 participants
- Enrollment target
Study Summary
The investigators aim is to augment the current process for surgical consent for patients undergoing urogynecological procedures by incorporating visual media. We propose that visual media will be an effective and efficient addition to the standard of care in urogynecological consents and will improve patient understanding and satisfaction. Our randomized controlled trial will investigate the effect of standardizing the consent for three urogynecologic procedures (vaginal hysterectomy, robotic sacrocolpopexy, and sub-urethral sling) using visual media, on patients' understanding of, and satisfaction with, their procedure. Our primary outcome will be patient's knowledge score at the end of the pre-operative clinic visit, and secondary outcomes include patients' satisfaction, subjective understanding of their procedure, immediate pre-operative and post-operative knowledge, and number of post-operative encounters. Participants will be followed up to their post-operative clinic visit.
Interventions
- OTHER Standardized visual presentation
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 64 participants |
| Start Date | 2014-12 |
| Est. Completion | 2018-08 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02313701
The ClinicalTrials.gov registry entry for NCT02313701 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 64 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Beth Israel Deaconess Medical Center, which has 488 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Standardized visual presentation is the first listed.
NCT02313701 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02313701 about?
NCT02313701 is a clinical study titled "Effect of Standardized Consent for Urogynecological Procedures on Patient Satisfaction". The investigators aim is to augment the current process for surgical consent for patients undergoing urogynecological procedures by incorporating visual media. We propose that visual media will be an effective and efficient addition to the standard of care in urogynecological consents and will impro...
What is the current status of trial NCT02313701?
This trial is currently completed. It is a NA study. The enrollment target is 64 participants. The study started on 2014-12. Estimated completion is 2018-08.
What interventions are being tested in trial NCT02313701?
The interventions under investigation include: Standardized visual presentation (OTHER).
Who is sponsoring clinical trial NCT02313701?
This trial is sponsored by Beth Israel Deaconess Medical Center, which has 488 total clinical trials registered on ClinicalTrials.gov.
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