Fibromyalgia: Interventions for Pain and Mood Regulation
Primary Purpose
Fibromyalgia
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Cognitive-behavioral
Mindfulness-acceptance
Pain Education
Sponsored by
About this trial
This is an interventional treatment trial for Fibromyalgia
Eligibility Criteria
Inclusion Criteria:
- Pain in at least 11 of 18 tenderpoints
- Able to participate in study assessments and group-based meetings
- Willing to be randomized to treatment condition
Exclusion Criteria:
- Unable to understand written and spoken English
- Involved in pain-related litigation
- Currently involved in psychological treatment for pain and/or mood symptoms
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Active Comparator
Arm Label
Cognitive-Behavioral Therapy
Mindfulness-acceptance Therapy
Education
Arm Description
Group-based cognitive-behavioral manualized treatment
Group-based mindfulness-acceptance manualized treatment
Group-based manualized pain education
Outcomes
Primary Outcome Measures
Physical Functioning
Assessed via the SF-36 physical functioning subscale (Reference: Ware JE, Sherbourne CD. The MOS 36-Item Short-Form Health Survey (SF-36: I. conceptual framework and item selection. Med Care 1992; 30(6):473-83.
Bodily Pain
Assessed via the SF-36 Bodily Pain subscale (Reference: Ware JE, Sherbourne CD. The MOS 36-Item Short-Form Health Survey (SF-36): I. conceptual framework and item selection. Med Care 1992; 30(6):473-83.
Vitality
Assessed via the SF-36 Vitality subscale (Reference: Ware JE, Sherbourne CD. The MOS 36-Item Short-Form Health Survey (SF-36): I. conceptual framework and item selection. Med Care 1992; 30(6):473-83.
Depressive symptoms
Assessed via the Hamilton Depression Inventory (Reference: Reynolds WM, Kobak KA. Reliability and validity of the Hamilton Depression Inventory: A paper-and-pencil version of the Hamilton Depression Rating Scale Clinical Interview. Psychological Assessment 1995; 7(4): 472-83.
Social Functioning
Assessed via the SF-36 Social Functioning subscale (Reference: Ware JE, Sherbourne CD. The MOS 36-Item Short-Form Health Survey (SF-36): I. conceptual framework and item selection. Med Care 1992; 30(6):473-83.
Secondary Outcome Measures
Full Information
NCT ID
NCT02683278
First Posted
February 7, 2016
Last Updated
February 16, 2016
Sponsor
Arizona State University
1. Study Identification
Unique Protocol Identification Number
NCT02683278
Brief Title
Fibromyalgia: Interventions for Pain and Mood Regulation
Official Title
Fibromyalgia: Interventions for Pain and Mood Regulation
Study Type
Interventional
2. Study Status
Record Verification Date
February 2016
Overall Recruitment Status
Completed
Study Start Date
November 2008 (undefined)
Primary Completion Date
October 2014 (Actual)
Study Completion Date
October 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Arizona State University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study compares the impact of cognitive-behavioral therapy for pain (CBT-P), mindful awareness and acceptance treatment (M), and arthritis education as an active control condition (E) on mental and physical health outcomes among adults with chronic pain due to fibromyalgia (FM).
Detailed Description
Both cognitive-behavioral and mindful-acceptance based treatments impact pain and disability in people with chronic pain conditions like fibromyalgia. However, these treatments target different mechanisms. The focus of CBT is on helping individuals manage their thoughts and behaviors related to pain. In contrast, the focus of M is on improving individuals' ability be aware of and accept their experiences, and to develop their positive emotional resources.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibromyalgia
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
170 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Cognitive-Behavioral Therapy
Arm Type
Experimental
Arm Description
Group-based cognitive-behavioral manualized treatment
Arm Title
Mindfulness-acceptance Therapy
Arm Type
Experimental
Arm Description
Group-based mindfulness-acceptance manualized treatment
Arm Title
Education
Arm Type
Active Comparator
Arm Description
Group-based manualized pain education
Intervention Type
Behavioral
Intervention Name(s)
Cognitive-behavioral
Intervention Description
Seven sessions of group-based treatment targeting skills to improve dysfunctional pain-related thoughts and behaviors
Intervention Type
Behavioral
Intervention Name(s)
Mindfulness-acceptance
Intervention Description
Seven sessions of group-based treatment targeting skills to improve mindful awareness and acceptance of pain and stress, and increase positive emotional experiences
Intervention Type
Other
Intervention Name(s)
Pain Education
Intervention Description
Seven sessions of group-based education to provide information regarding managing a chronic pain condition, but with no exercises to promote skill development
Primary Outcome Measure Information:
Title
Physical Functioning
Description
Assessed via the SF-36 physical functioning subscale (Reference: Ware JE, Sherbourne CD. The MOS 36-Item Short-Form Health Survey (SF-36: I. conceptual framework and item selection. Med Care 1992; 30(6):473-83.
Time Frame
Change from baseline, 6-mo followup, and 12-mo followup
Title
Bodily Pain
Description
Assessed via the SF-36 Bodily Pain subscale (Reference: Ware JE, Sherbourne CD. The MOS 36-Item Short-Form Health Survey (SF-36): I. conceptual framework and item selection. Med Care 1992; 30(6):473-83.
Time Frame
Change from baseline, 6-mo followup, and 12-mo followup
Title
Vitality
Description
Assessed via the SF-36 Vitality subscale (Reference: Ware JE, Sherbourne CD. The MOS 36-Item Short-Form Health Survey (SF-36): I. conceptual framework and item selection. Med Care 1992; 30(6):473-83.
Time Frame
Change from baseline, 6-mo followup, and 12-mo followup
Title
Depressive symptoms
Description
Assessed via the Hamilton Depression Inventory (Reference: Reynolds WM, Kobak KA. Reliability and validity of the Hamilton Depression Inventory: A paper-and-pencil version of the Hamilton Depression Rating Scale Clinical Interview. Psychological Assessment 1995; 7(4): 472-83.
Time Frame
Change from baseline, 6-mo followup, 12-mo followup
Title
Social Functioning
Description
Assessed via the SF-36 Social Functioning subscale (Reference: Ware JE, Sherbourne CD. The MOS 36-Item Short-Form Health Survey (SF-36): I. conceptual framework and item selection. Med Care 1992; 30(6):473-83.
Time Frame
Change from baseline, 6-mo followup, and 12-mo followup
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Pain in at least 11 of 18 tenderpoints
Able to participate in study assessments and group-based meetings
Willing to be randomized to treatment condition
Exclusion Criteria:
Unable to understand written and spoken English
Involved in pain-related litigation
Currently involved in psychological treatment for pain and/or mood symptoms
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mary Davis, Ph.D.
Organizational Affiliation
Arizona State University
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
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Fibromyalgia: Interventions for Pain and Mood Regulation
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