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N/A N=21 Other

Compassion-Based Resiliency Training (CBRT) Intervention on Racism-based Stress

Racism · Stress, Psychological

Enrolled (actual)
21
Serious AEs
4.8%
Results posted
Apr 2026
Primary outcome: Primary: Feasibility of Study — 19 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Contemplative-Based Resilience Training (CBRT) (Behavioral)
Age
Adult · 18+ yrs
Sex
All
Sponsor
Rockefeller University
Primary completion
Aug 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Feasibility of Study
19
PRIMARY
Acceptability of CBRT (Qualitative Interview Findings)
6; 17; 11; 5; 12
SECONDARY
Allostatic Load Composite Score (NHANES Clinically Relevant Scoring 0-11 )
2.11; 2 0.135
SECONDARY
Cortisol Awakening Response (CAR)
.100; -0.025 0.395
SECONDARY
Composite CTRA Gene Expression Score
6.20; 6.19 0.93
SECONDARY
Telomere Length

Summary

The primary aim of this study is to explore the feasibility, acceptability, and preliminary effectiveness of CBRT intervention among African Americans compared to a wait-list control group. The specific objectives include assessing feasibility, gathering participant feedback, evaluating CBRT's impact on psychological and biological outcomes, and exploring the mediating role of mindfulness. The study is a 1-group pretest-posttest design. 20 African American participants will be recruited from various sources and undergo baseline and follow-up assessments. The intervention involves a 10-week CBRT program focusing on mindfulness, compassion, self-awareness, and stress-reduction techniques. Measures include sociodemographics and psychological measures (race-based stress, depression, perceived stress, quality of life, social connectedness, sleep, and resilience) and biological measures ( allostatic load, saliva cortisol, telomere length, and gene expression. Data is collected at baseline and 10 weeks.

Eligibility Criteria

Inclusion Criteria

  • Self Identity as African American or Black
  • 18-50 years old
  • Fluent in English

Exclusion Criteria

  • History of significant pre-existing brain disease or injury (e.g., dementia, stroke, seizure disorder, and head injury with cognitive sequelae or loss of consciousness more than 30 minutes, seizure disorder)
  • Reported history of learning disability/mental retardation
  • Current Attention Deficit Hyperactive Disorder (ADHD), depression, bipolar disorder, post-traumatic stress disorder (PTSD), or psychotic disorder diagnosis
  • Current psychotropic medication (as these medications are known impacts on brain function) e.g. antipsychotics, antianxiety
  • Severe/chronic medical illness (e.g., reported HIV+ status, cardiovascular disease, liver disease/cirrhosis, chronic kidney disease, current/past cancer with radiation/chemotherapy treatment, etc.)
  • Current methadone/suboxone/buprenorphine (or similar) maintenance
  • Use of illicit substances other than cannabis within the past 90 days
  • Pregnant
  • Major life events in the last 30 days (hospitalization, marriage, death in the family of friends, disaster)
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT06146218). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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