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NCT05306665 · ClinicalTrials.gov registry record · NA

PREventing Pain After Surgery

A NA study of Spondylolisthesis and Spinal Stenosis, sponsored by Brigham and Women's Hospital.

Recruiting
Registry status
NA
Development phase
140
Enrollment target
1
Study location

NCT05306665 is a NA study of Spondylolisthesis and Spinal Stenosis that is actively recruiting participants, run by Brigham and Women's Hospital. The registered enrollment target is 140 participants, roughly in line with the 145-participant average among 18 other Spondylolisthesis trials with a reported enrollment target. The trial reports 1 study location across 1 state.

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The verdict

NCT05306665, a NA study of Spondylolisthesis and Spinal Stenosis, is actively recruiting participants, sponsored by Brigham and Women's Hospital.

RECRUITING
Registry status
NA
Development phase
140 participants
Enrollment target
1
Study location

Study Summary

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.

Interventions

  • BEHAVIORAL ACT intervention

Study Locations (1)

Massachusetts

  • Brigham and Women's Hospital - Chestnut Hill

Trial Details

FieldValue
Enrollment Target 140 participants
Start Date 2023-01-13
Est. Completion 2026-08-01
Phase NA

Sponsor

Brigham and Women's Hospital

937 total trials

What the Registry Record Tells You About NCT05306665

The ClinicalTrials.gov registry entry for NCT05306665 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 140 participants, a figure that helps gauge the scale of data the investigators plan to collect, roughly in line with the 145-participant average among 18 other Spondylolisthesis trials with a reported enrollment target. The listed sponsor is Brigham and Women's Hospital, which has 937 total studies on file at ClinicalTrials.gov.

The record links to 6 conditions, with Spondylolisthesis appearing as the primary indexed condition, and to 1 intervention - of which ACT intervention is the first listed.

NCT05306665 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.

Frequently Asked Questions

What is clinical trial NCT05306665 about?

NCT05306665 is a clinical study titled "PREventing Pain After Surgery". 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 preliminar...

What is the current status of trial NCT05306665?

This trial is currently recruiting. It is a NA study. The enrollment target is 140 participants. The study started on 2023-01-13. Estimated completion is 2026-08-01.

What conditions does trial NCT05306665 study?

This clinical trial studies the following conditions: Spondylolisthesis, Spinal Stenosis, Spondylosis, Pain, Back, Back Injuries.

What interventions are being tested in trial NCT05306665?

The interventions under investigation include: ACT intervention (BEHAVIORAL).

Who is sponsoring clinical trial NCT05306665?

This trial is sponsored by Brigham and Women's Hospital, which has 937 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05306665 being conducted?

This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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