Chronic Musculoskeletal Disease Clinical Trial
Official title:
Neural Mechanisms of Acceptance and Commitment Therapy for Chronic Pain: A Network-Based fMRI Approach
Verified date | August 2020 |
Source | University of New Hampshire |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Acceptance and Commitment Therapy (ACT) has been recognized as an effective,
non-pharmacologic treatment for a variety of CP conditions. However, little is known about
the neurologic mechanisms underlying ACT. The investigators conducted an ACT intervention in
women (n=9) with chronic musculoskeletal pain. Functional magnetic resonance imaging (fMRI)
data were collected pre- and post-ACT, and changes in functional connectivity (FC) were
measured using Network-Based Statistics (NBS). Behavioral outcomes were measured using
validated assessments such as the Acceptance & Action Questionnaire (AAQ-II), the Chronic
Pain Acceptance Questionnaire (CPAQ), the Center for Epidemiologic Studies Depression Scale
(CES-D), and the NIH Toolbox Neuro-QoLTM (Quality of Life in Neurological Disorders) scales.
Results suggest that, following the four-week ACT intervention, participants exhibited
reductions in brain activation within and between key networks including self-reflection
(default mode, DMN), emotion (salience, SN), and cognitive control (frontal parietal, FPN).
These changes in connectivity strength were correlated with changes in behavioral outcomes
including decreased depression and pain interference, and increased participation in social
roles. This study is one of the first to demonstrate that improved function across the DMN,
SN, and FPN may drive the positive outcomes associated with ACT. This study contributes to
the emerging evidence supporting the use of neurophysiological indices to characterize
treatment effects of alternative and complementary mind-body therapies.
Status | Completed |
Enrollment | 9 |
Est. completion date | June 15, 2020 |
Est. primary completion date | April 30, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - greater than or equal to 18 years of age - Chronic musculoskeletal pain duration for greater than or equal to 3 months - Pain interference greater than or equal to 4 on Brief Pain Inventory (BPI; 0-10 scale) - No known contraindication to participate - Access to regular transportation - No plans to move or become pregnant in the next 3 months - MRI safe - Personal cell phone with the ability to receive text messages and access web-based material (e.g. short surveys) Exclusion Criteria: - Unstable medical condition, including a movement disorder, such as restless leg syndrome or Parkinson's disease, a neurological disorder such as Alzheimer's disease, history of stroke or brain lesion, a psychiatric disorder such as schizophrenia or bipolar disorder - Significant cognitive impairment - Pregnancy(a test must be conducted on each scan day) - A recent history of: cancer, malignancy, accident or trauma, palliative care, acupuncture, chiropractic care, cognitive-based psychotherapy, other form of alternative care to treat pain condition - Metal in the body of any sort - implants, pacemaker, pins, screws |
Country | Name | City | State |
---|---|---|---|
United States | Communication Science and Disorders Research Laboratory, University of New Hampshier | Durham | New Hampshire |
Lead Sponsor | Collaborator |
---|---|
University of New Hampshire | University of Texas at Austin |
United States,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Change in self-reported measures of pain acceptance from pre-to post-ACT | Chronic Pain Acceptance Questionnaire (CPAQ) | Measured by comparison of pre-treatment (baseline) and 4-week post-treatment (within 1 week after treatment completion) assessment data | |
Other | Change in self-reported measures of pain interference from pre-to post-ACT | NIH Patient-Reported Outcome Measurement Information System (PROMIS) scale | Measured by comparison of pre-treatment (baseline) and 4-week post-treatment (within 1 week after treatment completion) assessment data | |
Other | Change in self-reported measures of acceptance and action from pre-to post-ACT | Acceptance & Action Questionnaire (AAQ-II) | Measured by comparison of pre-treatment (baseline) and 4-week post-treatment (within 1 week after treatment completion) assessment data | |
Primary | Change in Network Based Statistic (NBS) from pre-to post-ACT | Derived from fMRI data, the NBS the Network Based Statistic (NBS) is used to examine changes in functional connectivity from pre-to post ACT. | Measured by comparison of pre-treatment (baseline) and 4-weeks post-treatment (within 1 week after treatment completion) fMRI scan data | |
Secondary | Change in self-reported measures of depression from pre-to post-ACT | Depression Scale, as measured by the Center for Epidemiologic Studies Scale (CES-D) | Measured by comparison of pre-treatment (baseline) and 4-week post-treatment (within 1 week after treatment completion) assessment data | |
Secondary | Change in self-reported measures of satisfaction with social role from pre-to post-ACT | NIH Toolbox Neuro-QoLTM (Quality of Life in Neurological Disorders) scale | Measured by comparison of pre-treatment (baseline) and 4-week post-treatment (within 1 week after treatment completion) assessment data |
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