Clinical trial Recruiting at 1 site Interventional Ages 18 to 50

MB-Spirit program to improve psychological and spiritual well-being in stressed adults.

Official title: Assessing MB-Spirit: A Novel Intervention for Promoting Spiritual Development and Psychological Well-being

Run by Massachusetts General Hospital · NCT07325448 · Data updated 2026-11-12

This program will test whether an 8-week online MB-Spirit course helps adults with high stress improve spiritual well-being and psychological health and whether their brain scans change after the course.

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Quick facts

Study typeInterventional
Ages18 Years to 50 Years
SexAll
Enrollment44 (estimated)
SponsorMassachusetts General Hospital
Academic / other
Locations2 sites (Boston, Massachusetts and 1 other locations)
StatusRecruiting
StartedMarch 15, 2026
Main results expectedNovember 2026
Study endsNovember 2026
Registry record updatedJune 11, 2026
Trial IDNCT07325448 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are English-speaking adults with high stress who can attend eight weekly two-hour online sessions, travel to Boston for MRI scans, and who do not use psychotropic medications or have excluded medical or psychiatric conditions.

Probably not a fit

People with current psychotropic medication use, a history of psychosis or suicidality, significant neurological conditions, pregnancy, claustrophobia, MRI contraindications, left-handedness, or inability to travel to Boston are not eligible and are unlikely to benefit from this program.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Forty-four adults with high stress will be randomized 1:1, stratified by sex, to take an 8-week MB-Spirit course immediately or to a wait-list control. The course meets online for two hours each week and participants will complete questionnaires and a structured interview before and after the intervention while logging daily meditation practice in REDCap. Participants in the MB-Spirit arm will have pre- and post-intervention MRI scans including a high-resolution structural scan, resting-state fMRI, and guided meditation fMRI runs with in-scanner ratings of spiritual depth. Primary outcome is change in spiritual well-being, with secondary outcomes of mindfulness and character/virtue strengths and exploratory analyses of clinical symptoms.

Why it matters

Potential benefit: If successful, MB-Spirit could help stressed adults increase spiritual well-being, mindfulness, and related psychological functioning.

How similar studies have gone: Prior mindfulness-based programs have shown improvements in well-being and brain function, but MB-Spirit's explicit spiritual emphasis and its guided-meditation fMRI protocol are a novel combination.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Understands English
* Able to attend all 8 classes
* Able to travel to Boston for MRI scans

Exclusion Criteria:

* 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, homicidally, self-destructive acts, schizophrenia or psychosis.

Where it's running

  • 149 13th St
    Boston, Massachusetts, United States
    Recruiting
  • Charlestown Navy Yard Campus
    Boston, Massachusetts, United States
    Not yet recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.