Actively Recruiting
Mind-body Resilience Program for Cardiac Arrest Survivors and Their Caregivers: Recovering Together After Cardiac Arrest
Led by Massachusetts General Hospital · Updated on 2025-10-23
84
Participants Needed
1
Research Sites
141 weeks
Total Duration
On this page
Sponsors
M
Massachusetts General Hospital
Lead Sponsor
N
National Center for Complementary and Integrative Health (NCCIH)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this study is to pilot two resilience interventions for cardiac arrest survivors and their informal caregivers, Recovering Together after Cardiac Arrest 1 and Recovering Together after Cardiac Arrest 2 . The data the investigators gather in this study will be used to further refine the interventions.
CONDITIONS
Official Title
Mind-body Resilience Program for Cardiac Arrest Survivors and Their Caregivers: Recovering Together After Cardiac Arrest
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult cardiac arrest survivors with a new diagnosis of cardiac arrest and an identified primary caregiver
- Survivor scores greater than 5 on the Short Form of the Mini Mental State Exam indicating sufficient cognitive function
- Ability and willingness to participate in a hybrid in-person and live video intervention
- English-speaking adults aged 18 years or older
- At least one member of the survivor-caregiver pair has clinically significant emotional distress (score over 7 on the Hospital Anxiety and Depression Scale subscales)
You will not qualify if you...
- Active psychosis, mania, substance dependence, or suicidal intent requiring higher care
- Psychiatric or neurological conditions that prevent meaningful participation
- Caregiver who is also a cardiac arrest survivor
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Massachusetts General Hospital
Boston, Massachusetts, United States, 02114
Actively Recruiting
Research Team
A
Alexander Presciutti, PhD
CONTACT
S
Sara Bogan, BA
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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