Clinical Trial

Remote Mindfulness Training Following Early Life Adversity 2

Study acronym: ReMind 2
Completed
View on ClinicalTrials.gov →
Summary
This pilot study aims to evaluate the effects of a 10-week online Mindfulness-Based Stress Reduction (MBSR) intervention on stress and inflammatory outcomes in a sample of emerging adults with a history of early life adversity. 15 participants (ages 18-29) with a history of childhood trauma will receive online, group-based MBSR sessions over 10 weeks. At pre- and post-intervention, participants will complete laboratory assessments, including self-report questionnaires and blood sample collection to assess markers of inflammation. Data assessing subjective and physiological stress in daily life will be collected for one week at pre- and post-intervention. This preliminary data will be used to test effects of online MBSR on health-relevant outcomes among young adults with a history of childhood trauma.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2025-07-22; most recent amendment 2026-01-06.
Status change: Active, Not Recruiting → Completed 2026-01-06
Status change: Recruiting → Active, Not Recruiting 2025-09-08
Trial Details
NCT Number NCT07085052
Lead Sponsor University of Pittsburgh
Conditions Stress, Mindfulness, Early Life Adversity
Enrollment 15 participants
Start Date 2025-07-15
Primary Completion 2025-12-16 (estimated)
Study Completion 2025-12-16 (estimated)
Updated on ClinicalTrials.gov 2026-01-08