Evaluating a Chronic Pain Treatment Program
Primary Purpose
Chronic Musculoskeletal Pain
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Mind-body emotional awareness program
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Musculoskeletal Pain
Eligibility Criteria
Inclusion Criteria:
- Adults with chronic musculoskeletal pain, not accounted for by disease or tissue pathology, who are seeking or referred for this psychological treatment program
Exclusion Criteria:
- Autoimmune diseases
- Cancer pain
- Illiterate
- Cognitively impaired
- Too medically ill
Sites / Locations
- St. John Providence Health System
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Treatment group
Arm Description
This is the only group in the study. It consists of patients with chronic musculoskeletal pain who are receiving the treatment program
Outcomes
Primary Outcome Measures
Brief Pain Inventory
Secondary Outcome Measures
Center for Epidemiologic Studies--Depression Scale
Satisfaction with Life Scale
McGill Pain Questionnaire
Impact of Events Scale-Revised
Positive Affect Negative Affect Scale-Expanded Version
Full Information
NCT ID
NCT00861302
First Posted
March 12, 2009
Last Updated
June 18, 2012
Sponsor
Wayne State University
Collaborators
Blue Cross Blue Shield of Michigan Foundation
1. Study Identification
Unique Protocol Identification Number
NCT00861302
Brief Title
Evaluating a Chronic Pain Treatment Program
Official Title
Evaluating Outcomes and Response Profiles of a Psychological Treatment for People With Chronic Pain
Study Type
Interventional
2. Study Status
Record Verification Date
June 2012
Overall Recruitment Status
Completed
Study Start Date
September 2008 (undefined)
Primary Completion Date
November 2011 (Actual)
Study Completion Date
November 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Wayne State University
Collaborators
Blue Cross Blue Shield of Michigan Foundation
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This interventional study seeks to evaluate the overall outcomes of a novel, emotional awareness intervention for people with chronic musculoskeletal pain and determine which patients benefit the most from this intervention. The investigators also are evaluating the effects of brief emotional communication technique embedded in the pre-treatment assessment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Musculoskeletal Pain
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
72 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Treatment group
Arm Type
Experimental
Arm Description
This is the only group in the study. It consists of patients with chronic musculoskeletal pain who are receiving the treatment program
Intervention Type
Behavioral
Intervention Name(s)
Mind-body emotional awareness program
Intervention Description
This intervention, developed and offered by Dr. Howard Schubiner of St. John Providence Health System, consists of a single individual session with him, followed by four, classroom group sessions. The intervention includes expressive writing, mindfulness, and other techniques designed to enhance awareness and acceptance of the emotional factors underlying the chronic pain problem.
Primary Outcome Measure Information:
Title
Brief Pain Inventory
Time Frame
baseline, post-treatment, 3- and 6-month follow-ups
Secondary Outcome Measure Information:
Title
Center for Epidemiologic Studies--Depression Scale
Time Frame
baseline, post-treatment, 3- and 6-month follow-ups
Title
Satisfaction with Life Scale
Time Frame
baseline, post-treatment, 3- and 6-month follow-ups
Title
McGill Pain Questionnaire
Time Frame
baseline, post-treatment, 3- and 6-month follow-ups
Title
Impact of Events Scale-Revised
Time Frame
baseline, post-treatment, 3- and 6-month follow-ups
Title
Positive Affect Negative Affect Scale-Expanded Version
Time Frame
baseline, post-treatment, 3- and 6-month follow-ups
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adults with chronic musculoskeletal pain, not accounted for by disease or tissue pathology, who are seeking or referred for this psychological treatment program
Exclusion Criteria:
Autoimmune diseases
Cancer pain
Illiterate
Cognitively impaired
Too medically ill
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark A Lumley, Ph.D.
Organizational Affiliation
Wayne State University
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. John Providence Health System
City
Southfield
State/Province
Michigan
ZIP/Postal Code
48075
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
26800632
Citation
Burger AJ, Lumley MA, Carty JN, Latsch DV, Thakur ER, Hyde-Nolan ME, Hijazi AM, Schubiner H. The effects of a novel psychological attribution and emotional awareness and expression therapy for chronic musculoskeletal pain: A preliminary, uncontrolled trial. J Psychosom Res. 2016 Feb;81:1-8. doi: 10.1016/j.jpsychores.2015.12.003. Epub 2015 Dec 11.
Results Reference
derived
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Evaluating a Chronic Pain Treatment Program
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