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Predictors of Pain Relief From Mindfulness-based Stress Reduction (MBSR) in Multiple Forms of Chronic Pain Patients

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University of Michigan

Status

Completed

Conditions

Chronic Pain Syndrome

Treatments

Behavioral: MBSR treatment

Study type

Interventional

Funder types

Other

Identifiers

NCT04981925
HUM00187535

Details and patient eligibility

About

The overall objective of this study is to better understand how Mindfulness-based Stress Reduction (MBSR) is the most helpful in terms of management of chronic pain symptoms.

The studies hypothesis is that an Interventional Response Phenotyping study (light phenotyping) can identify individuals with different underlying mechanisms for their pain who thus respond differentially to evidence-based interventions for chronic pain disorders.

Full description

Participants enrolled in this study will receive 8 weeks of MBSR therapy and complete surveys at various time points pre-treatment - post treatment.

Enrollment

381 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria for MBSR Study

  • Ages 18+
  • Any form of self-reported chronic pain (except cancer related pain)

Exclusion criteria for MBSR study

  • Unable to speak and write English
  • Visual or hearing difficulties that would preclude participation
  • Chronic pain from cancer.

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

381 participants in 1 patient group

MBSR treatment
Experimental group
Treatment:
Behavioral: MBSR treatment

Trial contacts and locations

1

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Central trial contact

Elizabeth Banner; Todd Favorite, Ph.D.

Data sourced from clinicaltrials.gov

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