Ignite Creation Date:
2024-10-26 @ 3:41 PM
Last Modification Date:
2024-10-26 @ 3:41 PM
Study NCT ID:
NCT06625892
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-10-02
Brief Title:
Factors and Effects of Multidimensional Intervention on Kinesiophobia in Cardiac Surgery Patients
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Investigating the Related Factors and Outcome of Kinesiophobia and the Effects of Multidimensional Interventions in Cardiac Surgery Patients
Status:
RECRUITING
Status Verified Date:
2024-10
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 primary objective of this two-year research project is to investigate the status of activity fear its related factors and prognosis in cardiac surgery patients in the first year Subsequently the study aims to develop a comprehensive intervention strategy combining exercise with cognitive-behavioral approaches tailored for cardiac surgery patients and assess the effectiveness of this intervention on activity fear prognosis and quality of life in the second year
Detailed Description:
The study uses a convenient sampling method focusing on patients undergoing cardiac surgery in the cardiac surgery ward of the Central Medical Center The first-year research adopts a descriptive correlational and repeated-measures design while the second-year research employs an experimental design Participants are randomly assigned to either the experimental or control group The experimental group undergoes a 12-week multidimensional interventions while the control group receives no intervention Data are collected through structured questionnaires Data collection occurs at discharge two weeks post-discharge six weeks 12 weeks and 24 weeks
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