Viewing Study NCT06552104



Ignite Creation Date: 2024-10-26 @ 3:37 PM
Last Modification Date: 2024-10-26 @ 3:37 PM
Study NCT ID: NCT06552104
Status: COMPLETED
Last Update Posted: None
First Post: 2024-08-01

Brief Title: The Effects of Acupressure Applied to the Primiparous During Episiotomy
Sponsor: None
Organization: None

Study Overview

Official Title: The Effects of Acupressure Applied to the Primiparous During Episiotomy Repair on Pain and Anxiety Levels
Status: COMPLETED
Status Verified Date: 2024-09
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: This study was conducted to determine the effects of acupressure applied during episiotomy repair on pain and anxiety levels of the primiparous

The study was conducted as a randomized controlled trial with 126 pregnant women 63 women in the acupressure group and 63 women in the control who applied to a maternity hospital between June and December 2023 Acupressure was applied to the acupressure group twice during internal suturing and skin suturing by the researcher during the episiotomy repair Visual Analog Scale VAS was used a total of four times before and after the intervention to assess the pain scores of the participants while the Spielberger Manual for State-Trait Anxiety Inventory STAI was used after the second intervention to determine the anxiety levels of the participants
Detailed Description: Introduction This study was conducted to determine the effects of acupressure applied during episiotomy repair on pain and anxiety levels of the primiparous

Methods The study was conducted as a randomized controlled trial with 126 pregnant women 63 women in the acupressure group and 63 women in the control who applied to a maternity hospital between June and December 2023 Acupressure was applied to the acupressure group twice during internal suturing and skin suturing by the researcher during the episiotomy repair Visual Analog Scale VAS was used a total of four times before and after the intervention to assess the pain scores of the participants while the Spielberger Manual for State-Trait Anxiety Inventory STAI was used after the second intervention to determine the anxiety levels of the participants

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