Viewing Study NCT06555653



Ignite Creation Date: 2024-10-26 @ 3:37 PM
Last Modification Date: 2024-10-26 @ 3:37 PM
Study NCT ID: NCT06555653
Status: COMPLETED
Last Update Posted: None
First Post: 2024-08-02

Brief Title: The Effect of Video-based Multimedia Information Before Amniocentesis on Pain Anxiety and Pregnancy Outcomes
Sponsor: None
Organization: None

Study Overview

Official Title: The Effect of Video-based Multimedia Information Before Amniocentesis on Pain Anxiety and Pregnancy Outcomes
Status: COMPLETED
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this clinical trial is to assess the effect of video-based multimedia information before amniocentesis on pain anxiety and pregnancy outcomes
Detailed Description: Amniocentesis is the most commonly used invasive prenatal diagnostic test This study aimed to investigate the effect of video-based multimedia information MMI on the anxiety and pain levels of patients undergoing amniocentesis

All consecutive women aged 18-45 years scheduled for amniocentesis were included in this prospective randomized controlled study Subjects were assigned to receive video-based MMI or traditional written information controls Anxiety levels were assessed at the first admission using the State and Trait Anxiety Inventory-State STAI-S After MMI and written information STAI-S was repeated before the procedure A standard amniocentesis procedure was performed on all patients by the same perinatology physicians After amniocentesis a Likert scale was used to evaluate the ease of the procedure and patient satisfaction and a visual analog scale was used to evaluate pain Pregnancy results and amniocentesis results were noted

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None