Actively Recruiting
CCSH (Compassion-Centered Spiritual Health) for Teams
Led by Emory University · Updated on 2026-05-05
80
Participants Needed
2
Research Sites
61 weeks
Total Duration
On this page
Sponsors
E
Emory University
Lead Sponsor
N
National Center for Complementary and Integrative Health (NCCIH)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Emory Spiritual Health has developed a Compassion-Centered Spiritual Health group-based intervention, called CCSH Interventions for Teams, and are enrolling staff and providers into the groups in this randomized study design. The groups will meet once every other week for 60 minutes for 8 weeks (4 sessions total). The investigators will evaluate the feasibility and acceptability of this novel team-based intervention that includes mindfulness and compassion-based approaches with mixed-role oncology teams. Employees (n = 80; nurses, advanced practice providers (APPs), physicians, staff) working at an NCI- designated Comprehensive Cancer Center will be randomized by team (8-12 employees/group) to Compassion Centered Spiritual Health Team Intervention (CCSH-TI) or TAU (Treatment as Usual) group. The research objective is to evaluate the feasibility and acceptability of CCSH-TI, and to develop and validate a novel, low-burden ambulatory assessment "toolkit" to improve the measurement of psychological safety and burnout.
CONDITIONS
Official Title
CCSH (Compassion-Centered Spiritual Health) for Teams
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Full-time employees working in oncology teams at Winship Cancer Institute
- Employees working in intensive care at Emory University St. Joseph hospital
You will not qualify if you...
- Younger than 18 years old
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Emory Winship Cancer Institute
Atlanta, Georgia, United States, 30322
Actively Recruiting
2
Emory University St. Joseph hospital
Atlanta, Georgia, United States, 30342
Actively Recruiting
Research Team
J
Jennifer Mascaro, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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