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Breathwork for Chronic Musculoskeletal Pain

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Florida State University

Status

Completed

Conditions

Musculoskeletal Pain
Chronic Pain
Pain, Chronic
Pain

Treatments

Behavioral: Guided Resipiration Mindfulness Therapy (GRMT)

Study type

Interventional

Funder types

Other

Identifiers

NCT06455839
00005048

Details and patient eligibility

About

This project is a single-site, single-arm, clinical feasibility trial examining the impact of a single-session, 2-hour connected consciousness breathing with breath retention (CCBR) training for chronic musculoskeletal pain.

Full description

CCBR is a breathwork style that involves breathing with no pause between inhalation and exhalation (also known as circular breathing). This breathing pattern is maintained for a given period of time, ranging from 5 minutes to over 2 hours. In the proposed project, the CCBR training will begin with a 15-minute introduction to CCBR, followed by an hour and 15 minutes of therapist-guided CCBR practice. The final 30 minutes will be used to discuss participant experiences during the CCBR practice. CCBR training sessions will occur in-person and in a small group format (5 participants each).

Enrollment

10 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • having received a professional diagnosis of clinical levels of chronic pain
  • being able to not commit to another (new) treatment during the course of the study
  • understanding English instructions fluently
  • Being 18 and above

Exclusion criteria

  • having learned to practice breathwork any time in the past
  • being unable to perform most basic tasks due to pain or pain treatment.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

10 participants in 1 patient group

Guided Respiration Mindfulness Therapy
Experimental group
Treatment:
Behavioral: Guided Resipiration Mindfulness Therapy (GRMT)

Trial contacts and locations

1

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Central trial contact

Adam Hanley, PhD; Allison Davis, MS

Data sourced from clinicaltrials.gov

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