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Study of Opioid Use After Lumbar and Cervical Spine Surgery (SOULCS)

Primary Purpose

Low Back Pain, Opiate Addiction, Neck Pain

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Educational Video
Sponsored by
Brooke Army Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Low Back Pain focused on measuring patient education, low back pain, post-surgical pain, chronic opioid use, Neck Pain

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Currently scheduled for a pre-operative appointment with an orthopaedic spine surgeon or neurosurgeon specifically for a lumbar surgery.
  2. Surgery is taking place for a condition that has been ongoing for 6 months or longer (chronic)
  3. Between the age of 18 - 65 years
  4. Read and speak English well enough to understand the education, provide informed consent and follow study instructions

Exclusion Criteria:

a. Known aversion or allergy that would prevent the patient from taking any opioid based pain medication

Sites / Locations

  • Brooke Army Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Educational Video

Usual Care

Arm Description

Evidence-based video: Best Advice for People Taking Opioid Medication

Usual care education provided at time of pre-operative appointment.

Outcomes

Primary Outcome Measures

Number of Opioid Medication Prescriptions
Number of prescriptions within 12 months after surgery

Secondary Outcome Measures

Modified Oswestry Disability Index (ODI) or Neck Disability Index (NDI)
The ODI and NDI are 10-item scales with higher numbers indicating greater disability. Each item has 6 possible questions (0-5), which are then summed and multiplied to provide a % score out of 100%. The ODI focused on low back pain and the NDI on neck pain. As values are on the same scale, they were entered as one outcome since we included both neck and low back pain patients. Patients undergoing cervical spine surgery filled out the NDI (Neck Disability Index) and patients undergoing lumbar spine surgery filled out the ODI (Oswestry Disability Index)
Numeric Pain Rating Scale (NPRS)
A 0-10 numeric pain rating scale ('0' indicating no pain, and '10' worst imaginable pain) will be used to assess pain intensity.

Full Information

First Posted
February 2, 2016
Last Updated
July 13, 2022
Sponsor
Brooke Army Medical Center
Collaborators
Baylor University
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1. Study Identification

Unique Protocol Identification Number
NCT02674711
Brief Title
Study of Opioid Use After Lumbar and Cervical Spine Surgery
Acronym
SOULCS
Official Title
The Effect of a Brief Pre-operative Pain Medication Educational Video on Post-operative Prescription Opioid Medication Use in Patients Undergoing Spine Surgery. A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Completed
Study Start Date
August 2015 (Actual)
Primary Completion Date
February 28, 2017 (Actual)
Study Completion Date
June 1, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Brooke Army Medical Center
Collaborators
Baylor University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this project is to assess the impact of an educational video on the use of prescription opioid medication during a 6-month period following spine surgery. Subjects will be recruited from the pool of patients coming in for the pre-operative appointment prior to spine surgery. Patients that consent and enroll will be randomized to receive either a brief educational video at this appointment or usual care. Patients will be followed after surgery weekly for the first month, and then again at 6 months to determine their prescription opioid medication utilization patterns. Prescription data will also be pulled from electronic medical records.
Detailed Description
After consenting, meeting inclusion criteria, and enrollment, all participants will complete several standard self-report questionnaires related to medical history, social demographic, and psychosocial variables that are related to low back pain, and often used in clinics that manage patients with low back pain. They will then be randomized to either receive the education, or only usual care (which is the typical information the surgeon provides the patient verbally during the pre-operative appointment). All patients will receive the usual care education from their surgeon. Education Group: The educational video is a white board style patient-centric video. The content of the education focus on providing a historical perspective for opioid prescription from the time when the risk of dependence was highly underestimated. The video discusses the current evidence for the effect of opioid medications in non-cancer on-acute pain. It also discusses some of the dangers of long-term opioid usage. All Subjects: All subjects will receive the usual care education that is typically given by their surgeon. That will be left up to the discretion of each surgeon. All patients will proceed with the surgical procedure as planned. Each week during the 1-month period after the surgery, patients will be contacted, and then again at 6 months to ask history of prescription opioid utilization.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Low Back Pain, Opiate Addiction, Neck Pain
Keywords
patient education, low back pain, post-surgical pain, chronic opioid use, Neck Pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Educational Video
Arm Type
Experimental
Arm Description
Evidence-based video: Best Advice for People Taking Opioid Medication
Arm Title
Usual Care
Arm Type
No Intervention
Arm Description
Usual care education provided at time of pre-operative appointment.
Intervention Type
Behavioral
Intervention Name(s)
Educational Video
Other Intervention Name(s)
Best Advice for People Taking Opioid Medication
Intervention Description
The content of the education focus on providing a historical perspective for opioid prescription from the time when the risk of dependence was highly underestimated. The video discusses the current evidence for the effect of opioid medications in non-cancer non-acute pain. It also discusses some of the dangers of long-term opioid usage. The video is 11 and ½ minutes long.
Primary Outcome Measure Information:
Title
Number of Opioid Medication Prescriptions
Description
Number of prescriptions within 12 months after surgery
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Modified Oswestry Disability Index (ODI) or Neck Disability Index (NDI)
Description
The ODI and NDI are 10-item scales with higher numbers indicating greater disability. Each item has 6 possible questions (0-5), which are then summed and multiplied to provide a % score out of 100%. The ODI focused on low back pain and the NDI on neck pain. As values are on the same scale, they were entered as one outcome since we included both neck and low back pain patients. Patients undergoing cervical spine surgery filled out the NDI (Neck Disability Index) and patients undergoing lumbar spine surgery filled out the ODI (Oswestry Disability Index)
Time Frame
6 months
Title
Numeric Pain Rating Scale (NPRS)
Description
A 0-10 numeric pain rating scale ('0' indicating no pain, and '10' worst imaginable pain) will be used to assess pain intensity.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Currently scheduled for a pre-operative appointment with an orthopaedic spine surgeon or neurosurgeon specifically for a lumbar surgery. Surgery is taking place for a condition that has been ongoing for 6 months or longer (chronic) Between the age of 18 - 65 years Read and speak English well enough to understand the education, provide informed consent and follow study instructions Exclusion Criteria: a. Known aversion or allergy that would prevent the patient from taking any opioid based pain medication
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniel Rhon, DPT, DSc
Organizational Affiliation
Brooke Army Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Brooke Army Medical Center
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78234
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Any data sharing must first go through a Data Sharing Agreement approved by the Defense Health Agency.
IPD Sharing Time Frame
Available for 1 year
IPD Sharing Access Criteria
US Defense Health Agency data sharing agreement application approved
IPD Sharing URL
https://www.health.mil/Military-Health-Topics/Privacy-and-Civil-Liberties/Submit-a-Data-Sharing-Application
Citations:
PubMed Identifier
22786449
Citation
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Results Reference
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PubMed Identifier
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Citation
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Results Reference
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PubMed Identifier
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Citation
Devin CJ, Lee DS, Armaghani SJ, Bible J, Shau DN, Martin PR, Ehrenfeld JM. Approach to pain management in chronic opioid users undergoing orthopaedic surgery. J Am Acad Orthop Surg. 2014 Oct;22(10):614-22. doi: 10.5435/JAAOS-22-10-614.
Results Reference
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PubMed Identifier
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Citation
Walid MS, Hyer L, Ajjan M, Barth AC, Robinson JS Jr. Prevalence of opioid dependence in spine surgery patients and correlation with length of stay. J Opioid Manag. 2007 May-Jun;3(3):127-8, 130-2. doi: 10.5055/jom.2007.0050.
Results Reference
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PubMed Identifier
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Martell BA, O'Connor PG, Kerns RD, Becker WC, Morales KH, Kosten TR, Fiellin DA. Systematic review: opioid treatment for chronic back pain: prevalence, efficacy, and association with addiction. Ann Intern Med. 2007 Jan 16;146(2):116-27. doi: 10.7326/0003-4819-146-2-200701160-00006.
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Deshpande A, Furlan A, Mailis-Gagnon A, Atlas S, Turk D. Opioids for chronic low-back pain. Cochrane Database Syst Rev. 2007 Jul 18;(3):CD004959. doi: 10.1002/14651858.CD004959.pub3.
Results Reference
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Citation
Lee D, Armaghani S, Archer KR, Bible J, Shau D, Kay H, Zhang C, McGirt MJ, Devin C. Preoperative Opioid Use as a Predictor of Adverse Postoperative Self-Reported Outcomes in Patients Undergoing Spine Surgery. J Bone Joint Surg Am. 2014 Jun 4;96(11):e89. doi: 10.2106/JBJS.M.00865. Epub 2014 Jun 4.
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Citation
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Results Reference
result

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Study of Opioid Use After Lumbar and Cervical Spine Surgery

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