Mindfulness Based Stress Reduction for Healthy Subjects

Phase-Based Progress Estimates
1
Effectiveness
1
Safety
Healthy SubjectsMindfulness Based Stress Reduction - Behavioral
Eligibility
18 - 64
All Sexes
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Study Summary

This trial is investigating whether mind-body awareness training (in the form of yoga or meditation) can help people learn to use a brain computer interface more effectively.

Treatment Effectiveness

Study Objectives

1 Primary · 1 Secondary · Reporting Duration: 6 months for each participant. The overall project will last for 5 years.

Year 5
BCI Learning over BCI sessions
Proportion of proficient subjects

Trial Safety

Side Effects for

Stress Management Education
2%sleep disruption
This histogram enumerates side effects from a completed 2013 Phase 4 trial (NCT01033851) in the Stress Management Education ARM group. Side effects include: sleep disruption with 2%.

Trial Design

2 Treatment Groups

Waitlist
1 of 2
Mindfulness Based Stress Reduction
1 of 2

Active Control

Experimental Treatment

300 Total Participants · 2 Treatment Groups

Primary Treatment: Mindfulness Based Stress Reduction · No Placebo Group · N/A

Mindfulness Based Stress Reduction
Behavioral
Experimental Group · 1 Intervention: Mindfulness Based Stress Reduction · Intervention Types: Behavioral
WaitlistNoIntervention Group · 1 Intervention: Waitlist · Intervention Types:
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Mindfulness Based Stress Reduction
2012
Completed Phase 4
~3160

Trial Logistics

Trial Timeline

Screening: ~3 weeks
Treatment: Varies
Reporting: 6 months for each participant. the overall project will last for 5 years.

Who is running the clinical trial?

Carnegie Mellon UniversityLead Sponsor
70 Previous Clinical Trials
536,153 Total Patients Enrolled
Bin He, Ph.DPrincipal InvestigatorCarnegie Mellon University

Eligibility Criteria

Age 18 - 64 · All Participants · 4 Total Inclusion Criteria

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