Actively Recruiting

Phase Not Applicable
Age: 18Years - 85Years
All Genders
ID07406997

Rehabilitation With Empowered STrategies to Optimize REcovery After Spine Surgery

Led by Vanderbilt University Medical Center · Updated on 2026-06-01

100

Participants Needed

4

Research Sites

26 weeks

Total Duration

On this page

Sponsors

V

Vanderbilt University Medical Center

Lead Sponsor

U

United States Department of Defense

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of a remotely delivered behavioral intervention called Empowered Relief in patients undergoing lumbar spine surgery. This phase II randomized controlled trial aims to determine if Empowered Relief, given early after back surgery, can improve postoperative outcomes compared to a remotely delivered education session. The study also investigates how changes in pain catastrophizing relate to recovery and whether preoperative pain catastrophizing influences treatment response. Participants will be randomly assigned before surgery to one of two groups: a single remotely delivered group session of Empowered Relief, which focuses on pain neuroscience education and coping skills, or a single remotely delivered group education session about managing pain and recovery after back surgery. Both sessions are conducted online by licensed healthcare professionals. Participants will complete surveys before surgery and again at 3 and 6 months after surgery to assess outcomes such as pain interference, physical function, disability, pain intensity, and opioid use. Outcome assessments are done by evaluators who do not know the group assignments. Overall, the study will help advance research on non-drug remote strategies to improve quality of life after spine surgery in civilian and military patients.

CONDITIONS

Brief Title

Rehabilitation With Empowered STrategies to Optimize REcovery

Who Can Participate

Age: 18Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Scheduled for lumbar degenerative condition surgery using laminectomy with or without fusion
  • English speaking
  • Aged between 18 and 85 years
Not Eligible

You will not qualify if you...

  • Surgery due to trauma, fracture, tumor, infection, or spinal deformity
  • Revision surgery
  • Lumbar spine surgery in the past 12 months
  • Involved in litigation or workers' compensation claim related to injury
  • Currently receiving cancer treatment
  • No reliable internet connection
  • Unable to provide stable telephone or physical address
  • Unable to participate in follow-up assessments for 6 months after surgery

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 screening and enrollment visit

Treatment

Duration - 1 session before surgery

Participants attend a single remotely delivered group session with either behavioral strategies or educational information to support recovery after spine surgery.

1 remote group session

Follow-up

Duration - 6 months after surgery

Participants complete outcome assessments conducted by evaluators blinded to group assignment to evaluate pain interference, physical function, disability, pain intensity, and opioid use after surgery.

2 visits at 3 months and 6 months post-surgery

Trial Site Locations

Total: 4 locations

1

Tripler Army Medical Center

Honolulu, Hawaii, United States, 96859

Not Yet Recruiting

2

Vanderbilt University Medical Center

Nashville, Tennessee, United States, 37203

Actively Recruiting

3

Brooke Army Medical Center

Fort Sam Houston, Texas, United States, 78234

Not Yet Recruiting

4

Madigan Army Medical Center

Joint Base Lewis McChord, Washington, United States, 98431

Not Yet Recruiting

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Research Team

K

Kristin Archer, PhD

A

Amanda Priest

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Frequently Asked Questions

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