Ignite Creation Date:
2024-10-26 @ 3:35 PM
Last Modification Date:
2024-10-26 @ 3:35 PM
Study NCT ID:
NCT06517394
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-07-18
Brief Title:
Open Pilot Trial of a Mind-body Program for Cardiac Arrest Survivors and Their Caregivers
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Open Pilot Trial of a Dyadic Mind-body Program for Cardiac Arrest Survivors and Their Caregivers Recovering Together After Cardiac Arrest
Status:
NOT_YET_RECRUITING
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 purpose of this study is to pilot a mind-body intervention for cardiac arrest survivors and their informal caregivers Recovering Together after Cardiac Arrest The data the investigators gather in this study will be used to further refine our intervention
Detailed Description:
The goal of this study is to refine our proposed intervention Recovering Together after Cardiac Arrest RT-CA through an open pilot The investigators will deliver an open pilot of the intervention N5 dyads 10 participants total to evaluate initial feasibility and acceptability using exit interviews and pre-post assessments
The open pilot will take place at Massachusetts General Hospital intensive care units and step-down units Study clinicians will deliver 6 30 minute sessions of the intervention at bedside or on Zoomtelephone depending on participant preference and access All participants will complete measures at baseline and after completion of program 6 weeks At the completion of the program participants will engage in an exit interview where they will provide feedback of the intervention
The open pilot will take place at Massachusetts General Hospital intensive care units and step-down units Study clinicians will deliver 6 30 minute sessions of the intervention at bedside or on Zoomtelephone depending on participant preference and access All participants will complete measures at baseline and after completion of program 6 weeks At the completion of the program participants will engage in an exit interview where they will provide feedback of the intervention
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