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Pain Reprocessing Therapy vs Placebo and Usual Care for Chronic Back Pain
abstract
This abstract is available on the publisher's site.
Access this abstract nowImportance
Chronic back pain (CBP) is a leading cause of disability, and treatment is often ineffective. Approximately 85% of cases are primary CBP, for which peripheral etiology cannot be identified, and maintenance factors include fear, avoidance, and beliefs that pain indicates injury.
Objective
To test whether a psychological treatment (pain reprocessing therapy [PRT]) aiming to shift patients' beliefs about the causes and threat value of pain provides substantial and durable pain relief from primary CBP and to investigate treatment mechanisms.
Design, Setting, and Participants
This randomized clinical trial with longitudinal functional magnetic resonance imaging (fMRI) and 1-year follow-up assessment was conducted in a university research setting from November 2017 to August 2018, with 1-year follow-up completed by November 2019. Clinical and fMRI data were analyzed from January 2019 to August 2020. The study compared PRT with an open-label placebo treatment and with usual care in a community sample.
Interventions
Participants randomized to PRT participated in 1 telehealth session with a physician and 8 psychological treatment sessions over 4 weeks. Treatment aimed to help patients reconceptualize their pain as due to nondangerous brain activity rather than peripheral tissue injury, using a combination of cognitive, somatic, and exposure-based techniques. Participants randomized to placebo received an open-label subcutaneous saline injection in the back; participants randomized to usual care continued their routine, ongoing care.
Main Outcomes and Measures
One-week mean back pain intensity score (0 to 10) at posttreatment, pain beliefs, and fMRI measures of evoked pain and resting connectivity.
Results
At baseline, 151 adults (54% female; mean [SD] age, 41.1 [15.6] years) reported mean (SD) pain of low to moderate severity (mean [SD] pain intensity, 4.10 [1.26] of 10; mean [SD] disability, 23.34 [10.12] of 100) and mean (SD) pain duration of 10.0 (8.9) years. Large group differences in pain were observed at posttreatment, with a mean (SD) pain score of 1.18 (1.24) in the PRT group, 2.84 (1.64) in the placebo group, and 3.13 (1.45) in the usual care group. Hedges g was -1.14 for PRT vs placebo and -1.74 for PRT vs usual care (P < .001). Of 151 total participants, 33 of 50 participants (66%) randomized to PRT were pain-free or nearly pain-free at posttreatment (reporting a pain intensity score of 0 or 1 of 10), compared with 10 of 51 participants (20%) randomized to placebo and 5 of 50 participants (10%) randomized to usual care. Treatment effects were maintained at 1-year follow-up, with a mean (SD) pain score of 1.51 (1.59) in the PRT group, 2.79 (1.78) in the placebo group, and 3.00 (1.77) in the usual care group. Hedges g was -0.70 for PRT vs placebo (P = .001) and -1.05 for PRT vs usual care (P < .001) at 1-year follow-up. Longitudinal fMRI showed (1) reduced responses to evoked back pain in the anterior midcingulate and the anterior prefrontal cortex for PRT vs placebo; (2) reduced responses in the anterior insula for PRT vs usual care; (3) increased resting connectivity from the anterior prefrontal cortex and the anterior insula to the primary somatosensory cortex for PRT vs both control groups; and (4) increased connectivity from the anterior midcingulate to the precuneus for PRT vs usual care.
Conclusions and Relevance
Psychological treatment centered on changing patients' beliefs about the causes and threat value of pain may provide substantial and durable pain relief for people with CBP.
Additional Info
Disclosure statements are available on the authors' profiles:
Effect of Pain Reprocessing Therapy vs Placebo and Usual Care for Patients With Chronic Back Pain: A Randomized Clinical Trial
JAMA Psychiatry 2022 Jan 01;79(1)13-23, YK Ashar, A Gordon, H Schubiner, C Uipi, K Knight, Z Anderson, J Carlisle, L Polisky, S Geuter, TF Flood, PA Kragel, S Dimidjian, MA Lumley, TD WagerFrom MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
Although chronic low back pain (CLBP) is a major cause for disability, approximately 85% of patients do not have a clear pathologic cause of pain. MRIs typically reveal findings such as degenerative disc disease, bulging discs, facet arthropathy, and spinal stenosis; however, these findings are seen in a majority of individuals who are asymptomatic.1 In addition, medical treatment for CLBP is often ineffective. Randomized controlled trials (RCTs) have not shown surgery to be more effective than conservative forms for treatment2 and injections generally fare no better than placebo injections in meta-analyses of RCTs.3
The emergence of the neuroscience theories of predictive processing and clinical data suggest that the brain plays a major role in the precipitation, maintenance, and reinforcement of CLBP.4 This study was conducted to determine if a novel psychological intervention could alter central neural circuits and reduce pain. A total of 151 adults with CLBP were randomized to three arms: 1) a treatment as usual (TAU) arm; 2) an open-label placebo back injection arm; and 3) an arm treated with a single medical assessment followed by 8 individual psychotherapy sessions (over 4 weeks) of pain reprocessing therapy (PRT). The medical assessment determined that 43 of the 45 participants who entered the PRT treatment arm did not have a clear pathologic cause of pain, and these participants were educated on the major role of the brain in generating real physical pain. The PRT therapy is designed to demonstrate through a series of exercises that pain is not indicative of tissue damage and that it can be reversed by changing the mental perception of the pain and engaging in physical activities with less fear of the pain itself. In addition, fMRI scans were performed on all the participants before treatment and at a 1 month follow-up visit.
Of the 151 participants, the mean age was 41, the mean pain score was 4.1 of 10, mean disability score was 23 of 100, and the mean duration of pain was 10 years. After 1 month, 33 of the 50 participants (66%) assigned to the PRT arm (and 75% of the 44 who actually received PRT) were pain-free or nearly pain-free (pain scores of 0-1); compared with 10 of 51 (20%) of those assigned to the placebo injection arm and 5 of 50 (10%) assigned to the TAU arm. This result was highly significant, both statistically and clinically. Treatment outcomes were highly correlated with a changing attribution of pain from a peripheral injury to brain-generated pain in the absence of tissue damage. The results were largely maintained at a 1-year follow-up evaluation.
fMRI revealed several findings in the PRT treatment arm, including reduced anterior insula responses and increased connectivity of the prefrontal cortex and insula regions to the somatosensory and anterior midcingulate cortices. These findings are consistent with other studies showing neural circuitry involved in pain reduction.
This study demonstrated that it is possible to reverse CLBP in a majority of individuals when they are exposed to a different model for causation of pain and treatment is specifically directed towards achieving pain elimination, rather than pain management. Future studies that replicate these findings in more diverse populations with a larger set of therapists are needed. If replicated, this model could offer relief for millions with chronic functional pain syndromes. It should be noted that this model has also been used clinically with tension and migraine headaches, irritable bowel syndrome, pelvic pain syndromes, and chronic fatigue.
Primary care doctors can help their patients with CLBP by doing the following:
References