Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06949007

Yoga for Persistent Post-Surgical Pain (PPSP)

Led by Brigham and Women's Hospital · Updated on 2026-04-28

50

Participants Needed

1

Research Sites

173 weeks

Total Duration

On this page

Sponsors

B

Brigham and Women's Hospital

Lead Sponsor

N

National Center for Complementary and Integrative Health (NCCIH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The overall goal of this project is to complete a pilot feasibility randomized controlled trial (RCT) to inform a future fully-powered translational study evaluating yoga for management and resolution of persistent-post surgical pan (PPSP) and the role of biological, psychophysical, and psychosocial modulators in PPSP resolution.

CONDITIONS

Official Title

Yoga for Persistent Post-Surgical Pain (PPSP)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • History of torso surgeries such as thoracotomy, sternotomy, mastectomy, breast implant, open abdominal surgeries, or cesarean section
  • Completion of surgery alone or surgery with complementary pharmacological treatment
  • 18 years of age or older
  • Persistent post-surgical pain for at least 3 months with a pain severity of 4 or higher on the Brief Pain Inventory
  • Access to reliable transportation for study visits and yoga classes
  • Confirmed access to and proficiency with a smartphone, computer, or tablet
  • Fluent in English
Not Eligible

You will not qualify if you...

  • History of joint replacement, amputation, orthopedic (except thoracotomy and sternotomy), or other non-torso surgeries
  • Health conditions that make it difficult to follow the study protocol, including renal dialysis, cognitive impairment, serious neurological or psychiatric disorders, unstable cardiovascular disease, metastatic cancer, serious chronic medical conditions
  • Planned surgery during the intervention period
  • Chronic inflammatory systemic diseases such as rheumatoid arthritis
  • Active acute or chronic infections requiring antibiotics
  • Unmanaged hearing or visual impairments that affect participation in virtual classes
  • Substance use disorder
  • Pregnancy or intention to become pregnant within the next six months
  • Recent (last 3 months) or current participation in weekly mind-body movement therapies like yoga, tai chi, qigong, physical therapy, massage, or chiropractic care
  • Recent interventional pain management procedures (e.g., corticosteroid injection, trigger point injection, radiofrequency ablation) in the cervical or lumbar region within 4 weeks or scheduled during the study timeframe

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Mass General Brigham

Boston, Massachusetts, United States, 02215

Actively Recruiting

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Research Team

D

Dennis Munoz-Vergara, DVM, MS, MPH

CONTACT

P

Peter Wayne, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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