Viewing Study NCT06590389



Ignite Creation Date: 2024-10-26 @ 3:39 PM
Last Modification Date: 2024-10-26 @ 3:39 PM
Study NCT ID: NCT06590389
Status: COMPLETED
Last Update Posted: None
First Post: 2024-07-07

Brief Title: The Effect Of Mandala Activity On Postoperative Pain And Anxiety Levels In Gynecological Oncology Patients
Sponsor: None
Organization: None

Study Overview

Official Title: The Effect Of Mandala Activity On Postoperative Pain And Anxiety Levels In Gynecological Oncology Patients
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 designed as a randomised controlled 2-group pre-test post-test comparative experimental study to examine the effect of mandala activity on postoperative pain anxiety levels and analgesia use of gynaecological oncology patients
Detailed Description: This study was designed as a randomised controlled 2-group pre-test post-test comparative experimental study to examine the effect of mandala activity on postoperative pain anxiety levels and analgesia use of gynaecological oncology patients

The study was conducted with 42 patients who underwent open abdominal hysterectomy surgery in the Gynecological Oncology Surgery Clinic of a training and research hospital in Istanbul between 1 February 2023 and 1 August 2023 Patients in the intervention group n21 received mandala activity at least once a day during their postoperative hospitalisation days 0-2 Patients in the control group n21 did not receive any intervention Introductory Information Form Visual Analogue Scale VAS State-Trait Anxiety Inventory STAI-I Postoperative Patient Evaluation Form and Mandala Activity Booklet were used in the study

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