PREventing Pain After Surgery

Recruiting N/A Interventional Study
Pain, Back Spinal Stenosis Disc Herniation Spondylosis Spondylolisthesis Back Injuries
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
22 and older
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
140 (estimated)
Sponsor
Brigham and Women's Hospital · Other
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About This Trial
The present study aims to adapt and modify a brief presurgical Acceptance and Commitment Therapy (ACT) intervention aimed at preventing the transition to Chronic Post-Surgical Pain (CPSP) and reducing long-term opioid use. Investigators will then assess the acceptability, feasibility, and preliminary efficacy of the finalized intervention to prevent the transition to CPSP and reduce post-surgical …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * scheduled to undergo fusion, discectomy, vertebroplasty, kyphoplasty, or foraminotomy * age 22 and older * able to communicate fluently in English Exclusion Criteria: * inability to complete study procedures due to delirium, dementia, psychosis, or other cognitive impairment…
Contacts

Samantha M Meints, PhD

6177329014

smeints@bwh.harvard.edu

CONTACT

Marise Cornelius, MBA

mcornelius@bwh.harvard.edu

CONTACT