Viewing Study NCT06449118



Ignite Creation Date: 2024-06-16 @ 11:51 AM
Last Modification Date: 2024-10-26 @ 3:31 PM
Study NCT ID: NCT06449118
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-06-07
First Post: 2024-05-27

Brief Title: Effectiveness of Mindfulness-based Stress Reduction Program
Sponsor: Muş Alparlan University
Organization: Muş Alparlan University

Study Overview

Official Title: The Effect of Mindfulness Based-stress Reduction Program Applied to Parents With Physically Disabled Children on Stress and Quality of Life A Single-Blind Randomized Controlled Trial
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Having a physically disabled child presents serious challenges for parents not only in the practice of daily living but also on a psychological and emotional level In addition to meeting the constant and complex needs of their children these parents must also maintain their own emotional balance and psychological well-being In the long term high stress levels can seriously compromise parents mental health and reduce their overall quality of life Therefore the development of effective stress management strategies and psychological support mechanisms for parents is critical not only for individual well-being but also for the health of family relationships Mindfulness practices in this context emerge as powerful tools with the potential to increase parents ability to cope with stress and improve emotional well-being Therefore this study aims to determine the effect of the mindfulness stress reduction program applied to parents of physically disabled children on stress and quality of life
Detailed Description: None

Study Oversight

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