PREventing Pain After Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age22+
SponsorBrigham and Women's Hospital

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 opioid use six months following lumbar spine surgery. Finally, investigators will identify psychosocial and psychophysical phenotypes associated with response to this intervention.

Eligibility criteria

Qualifiers

scheduled to undergo fusion, discectomy, vertebroplasty, kyphoplasty, or foraminotomy

age 22 and older

able to communicate fluently in English

Disqualifiers

inability to complete study procedures due to delirium, dementia, psychosis, or other cognitive impairment

have a history of severe neurologic movement disorder

are pregnant or intent to become pregnant during study

have undergone previous spinal surgery

Trial design

Treatments tested in this trial

  • ACT intervention

Treatment groups

140 Participants
are divided into 2 treatment groups

Sponsors and collaborators