Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
All Genders
Healthy Volunteers
NCT07325448

Assessing MB-Spirit for Psychological Well-being

Led by Sara W Lazar · Updated on 2026-03-20

44

Participants Needed

2

Research Sites

33 weeks

Total Duration

On this page

Sponsors

S

Sara W Lazar

Lead Sponsor

H

Harvard Medical School (HMS and HSDM)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to learn if a new behavioral intervention, MB-Spirit, can improve well-being in stressed adults. The main questions it aims to answer are: 1. Can MB-Spirit improve well-being? 2. What brain changes accompany participation in MB-Spirit? Participants will: 1. Be enrolled in an online course that meets for two hours every week for 8-weeks. 2. Complete questionnaires before and after the course. 3. Complete an MRI scan of their brain before and after the course. Participants will be randomized to either take the course right away, or be put on a wait-list. Those on the wait-list will undergo the testing at 2 timepoints before they start the program.

CONDITIONS

Official Title

Assessing MB-Spirit for Psychological Well-being

Who Can Participate

Age: 18Years - 50Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Understands English
  • Able to attend all 8 classes
  • Able to travel to Boston for MRI scans
Not Eligible

You will not qualify if you...

  • Claustrophobia
  • Pregnancy
  • Head trauma
  • Metallic implants or devices contraindicating MRI
  • Left-handed
  • Conditions that alter cerebral blood flow or metabolism (e.g., stroke)
  • Current use of psychotropic medications
  • Lifetime history of suicidality, homicidality, or self-destructive acts
  • Schizophrenia or psychosis

AI-Screening

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Trial Site Locations

Total: 2 locations

1

149 13th St

Boston, Massachusetts, United States, 02129

Actively Recruiting

2

Charlestown Navy Yard Campus

Boston, Massachusetts, United States, 02129

Not Yet Recruiting

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Research Team

S

Sara Lazar, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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