Chronic Musculoskeletal Disease Clinical Trial
Official title:
Neural Mechanisms of Acceptance and Commitment Therapy for Chronic Pain: A Network-Based fMRI Approach
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.
Over 100 million Americans suffer from chronic pain (CP), which causes more disability than
any other medical condition in the U.S. at a cost of $560-$635 billion per year. Opioid
analgesics are frequently used to treat CP. However, long term use of opioids can cause brain
changes such as opioid-induced hyperalgesia that, over time, increase pain sensation. Also,
opioids fail to treat complex psychological factors that worsen pain-related disability,
including beliefs and emotional responses to pain. Cognitive behavioral therapy (CBT) can be
efficacious for CP. However, CBT does not focus on important factors needed for long-term
functional improvement, including attainment of personal goals and the psychological
flexibility to choose responses to pain.
Acceptance and Commitment Therapy (ACT) is a mindfulness-based therapy that focuses on
enabling individuals to accept what is out of their control, and to commit to valued actions
that enrich their lives. ACT was developed in 1986 by Stephen C. Hayes who began to examine
how language and thought influence internal experiences. By emphasizing acceptance instead of
avoidance, ACT differs from many other forms of cognitive behavioral therapy. Although not
originally designed for CP, ACT has been shown to be efficacious in terms of clinical
outcomes, adherence to treatment, and retention, earning the status of a "well-established"
treatment for CP from the American Psychological Association. ACT aims to increase
psychological flexibility, and has been associated with improved health outcomes in many
randomized controlled clinical trials, including three systematic reviews specific to CP.
Psychological flexibility is defined as an individual's ability to "recognize and adapt to
various situational demands; shift mindsets or behavioral repertoires when these strategies
compromise personal or social functioning; maintain balance among important life domains; and
be aware, open, and committed to behaviors that are congruent with deeply held values." ACT
is a "third wave" behavioral treatment that has been shown to be efficacious for treating CP,
as well as co-morbid conditions and factors (e.g., goal selection) related to long-term
functional improvement. Additionally, patients who participate in ACT report greater
long-term satisfaction compared to CBT. ACT is transdiagnostic and associated with
improvements in physical functioning and pain-related disability, as well as decreases in
emotional distress regardless of perceived pain intensity.
Resting-state functional magnetic resonance imaging (rsfMRI) allows for data to be collected
while individuals with CP rest in the MRI scanner for a short period of time (<10 minutes).
Thus, data provides information about the natural state of brain function in CP without
having to apply any external sensory or cognitive stimulation. Analysis methods of rsfMRI
have focused on multiple regions in the brain, targeting inherent and altered measures of
connectivity between brain regions and within brain networks. Further, alterations in brain
structure and function have been demonstrated in multiple CP syndromes. Prior imaging
research has suggested that CP results in abnormal hyper-connectivity of brain networks
associated with self-reflection (default mode, DMN), emotion (salience, SN), and cognitive
control (frontal parietal, FPN) networks. While ACT has been successful in helping those with
CP create a more functional and personally meaningful life, a critical gap in the
understanding of the neural mechanisms underlying ACT remains.
Only two prior investigations have used fMRI to assess neural mechanisms of ACT-based
interventions for CP. The first investigated task fMRI activation using pressure evoked pain.
Participants with fibromyalgia showed increased activation in the ventrolateral prefrontal
cortex (vlPFC) and orbitofrontal cortex (OFC) post-ACT after 12 weeks of ACT. Additionally,
results showed pain-evoked changes in connectivity between the vlPFC and thalamus after ACT.
Researchers in the second investigation conducted an 8-week ACT intervention vs. health
education control (HEC) for participants with comorbid CP and opioid addiction. Focusing on
DMN and pain regions in the brain, participants receiving ACT exhibited decreased activation
during evoked pain in the middle frontal gyrus (MFG), inferior parietal lobule (IPL), insula,
anterior cingulate cortex (aCC), posterior cingulate cortex (pCC), and superior temporal
gyrus (STG) compared with HEC participants.
In the present study, ACT was delivered to nine women with CP. fMRI was used to identify
changes in brain networks underlying ACT-related behavioral outcomes in CP. Based on prior
work examining ACT in CP, the investigators hypothesize that: (1) ACT will reduce
connectivity strength within and between the DMN, SN, and FPN, and that (2) changes in
connectivity strength will correlate with changes in behavioral outcomes from pre- to
post-ACT.
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