Skip to main content
Clinical Trials/NCT06555653
NCT06555653
Completed
N/A

The Effect of Video-based Multimedia Information Before Amniocentesis on Pain, Anxiety and Pregnancy Outcomes

Başakşehir Çam & Sakura City Hospital1 site in 1 country160 target enrollmentDecember 1, 2023

Overview

Phase
N/A
Intervention
Not specified
Conditions
Amniocentesis
Sponsor
Başakşehir Çam & Sakura City Hospital
Enrollment
160
Locations
1
Primary Endpoint
To assess the effect of video based information on pain levels
Status
Completed
Last Updated
last year

Overview

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

Registry
clinicaltrials.gov
Start Date
December 1, 2023
End Date
June 20, 2024
Last Updated
last year
Study Type
Observational
Sex
Female

Investigators

Sponsor
Başakşehir Çam & Sakura City Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • All consecutive women aged 18-45 years scheduled for amniocentesis

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

To assess the effect of video based information on pain levels

Time Frame: 01.12.2023- 01.04.2024

Subjects were assigned to receive video-based MMI or traditional written information (controls). A standard amniocentesis procedure was performed on all patients by the same perinatology physicians. After amniocentesis a visual analog scale was used to evaluate pain.

To assess the effect of video based information on anxiety

Time Frame: 01.12.2023- 01.04.2024

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.

To assess the effect of video based information on pregnancy outcome

Time Frame: 01.12.2023- 01.04.2024

Subjects were assigned to receive video-based MMI or traditional written information (controls).The birth outcomes were compared between the two groups in terms of live birth, termination of pregnancy, and intrauterine death.

To assess the effect of video based information on ease of procedure

Time Frame: 01.12.2023- 01.04.2024

Subjects were assigned to receive video-based MMI or traditional written information (controls). 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,

Study Sites (1)

Loading locations...

Similar Trials