Viewing Study NCT06522503



Ignite Creation Date: 2024-10-26 @ 3:36 PM
Last Modification Date: 2024-10-26 @ 3:36 PM
Study NCT ID: NCT06522503
Status: ENROLLING_BY_INVITATION
Last Update Posted: None
First Post: 2024-07-12

Brief Title: Effect of Stress Ball on Perceived Stress Pain and Satisfaction in Cancer Patients
Sponsor: None
Organization: None

Study Overview

Official Title: The Effect of a Stress Ball on Perceived Stress Pain and Satisfaction in Cancer Patients A Distraction-Based Intervention
Status: ENROLLING_BY_INVITATION
Status Verified Date: 2024-07
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 objective of this study was to ascertain the impact of stress ball utilisation on perceived stress pain and satisfaction levels during port catheter intervention in cancer patients In this study which was conducted in a randomised controlled design a control group of cancer patients receiving chemotherapy n37 was assigned to receive standard care during port catheter needle insertion An intervention group n37 was also formed comprising patients who received stress ball application in addition to standard care The intervention group was provided with a stress ball in both hands five minutes prior to the insertion of the port catheter needle and instructed to squeeze the ball in their hands at regular intervals until the conclusion of the procedure Prior to the application the descriptive characteristics of both groups were ascertained and their perceived stress levels were assessed Subsequently the pain and perceived stress levels of both groups were documented Additionally the satisfaction levels of the intervention group regarding the stress ball application were evaluated
Detailed Description: None

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