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Randomized Controlled Trial
. 2023 Sep 5;6(9):e2333846.
doi: 10.1001/jamanetworkopen.2023.33846.

Reattribution to Mind-Brain Processes and Recovery From Chronic Back Pain: A Secondary Analysis of a Randomized Clinical Trial

Affiliations
Randomized Controlled Trial

Reattribution to Mind-Brain Processes and Recovery From Chronic Back Pain: A Secondary Analysis of a Randomized Clinical Trial

Yoni K Ashar et al. JAMA Netw Open. .

Abstract

Importance: In primary chronic back pain (CBP), the belief that pain indicates tissue damage is both inaccurate and unhelpful. Reattributing pain to mind or brain processes may support recovery.

Objectives: To test whether the reattribution of pain to mind or brain processes was associated with pain relief in pain reprocessing therapy (PRT) and to validate natural language-based tools for measuring patients' symptom attributions.

Design, setting, and participants: This secondary analysis of clinical trial data analyzed natural language data from patients with primary CBP randomized to PRT, placebo injection control, or usual care control groups and treated in a US university research setting. Eligible participants were adults aged 21 to 70 years with CBP recruited from the community. Enrollment extended from 2017 to 2018, with the current analyses conducted from 2020 to 2022.

Interventions: PRT included cognitive, behavioral, and somatic techniques to support reattributing pain to nondangerous, reversible mind or brain causes. Subcutaneous placebo injection and usual care were hypothesized not to affect pain attributions.

Main outcomes and measures: At pretreatment and posttreatment, participants listed their top 3 perceived causes of pain in their own words (eg, football injury, bad posture, stress); pain intensity was measured as last-week average pain (0 to 10 rating, with 0 indicating no pain and 10 indicating greatest pain). The number of attributions categorized by masked coders as reflecting mind or brain processes were summed to yield mind-brain attribution scores (range, 0-3). An automated scoring algorithm was developed and benchmarked against human coder-derived scores. A data-driven natural language processing (NLP) algorithm identified the dimensional structure of pain attributions.

Results: We enrolled 151 adults (81 female [54%], 134 White [89%], mean [SD] age, 41.1 [15.6] years) reporting moderate severity CBP (mean [SD] intensity, 4.10 [1.26]; mean [SD] duration, 10.0 [8.9] years). At pretreatment, 41 attributions (10%) were categorized as mind- or brain-related across intervention conditions. PRT led to significant increases in mind- or brain-related attributions, with 71 posttreatment attributions (51%) in the PRT condition categorized as mind- or brain-related, as compared with 22 (8%) in control conditions (mind-brain attribution scores: PRT vs placebo, g = 1.95 [95% CI, 1.45-2.47]; PRT vs usual care, g = 2.06 [95% CI, 1.57-2.60]). Consistent with hypothesized PRT mechanisms, increases in mind-brain attribution score were associated with reductions in pain intensity at posttreatment (standardized β = -0.25; t127 = -2.06; P = .04) and mediated the effects of PRT vs control on 1-year follow-up pain intensity (β = -0.35 [95% CI, -0.07 to -0.63]; P = .05). The automated word-counting algorithm and human coder-derived scores achieved moderate and substantial agreement at pretreatment and posttreatment (Cohen κ = 0.42 and 0.68, respectively). The data-driven NLP algorithm identified a principal dimension of mind and brain vs biomechanical attributions, converging with hypothesis-driven analyses.

Conclusions and relevance: In this secondary analysis of a randomized trial, PRT increased attribution of primary CBP to mind- or brain-related causes. Increased mind-brain attribution was associated with reductions in pain intensity.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr Ashar reported receiving consulting fees from Lin Health, personal fees for clinical training from Pain Reprocessing Therapy Center and Mental Health Partners of Boulder County during the conduct of the study. Dr Lumley reported personal fees from Cognifisense, Inc outside the submitted work. Dr Perlis reported personal fees from Psy Therapeutics, Genomind, Burrage Capital, Circular Genomics, and Vault Health outside the submitted work. Dr Liston reported receiving consulting fees from Compass Pathways PLC, Delix Therapeutics, and Brainify.AI outside the submitted work. Dr Wager service on the advisory board for Curable Health Scientific and personal fees from Flomenhaft Law Firm outside the submitted work.

Figures

Figure 1.
Figure 1.. Study Flow Diagram
Figure 2.
Figure 2.. Pain Attribution Category Prevalence
Pain attributions were assigned to categories by coders masked to treatment condition and time point. Attribution category prevalence rates for each condition at each time point are shown, with each participant contributing 3 attributions. Substantial increases in psychological and brain attributions (psychological, brain, and stress categories) were observed in the PRT condition, with relatively little attribution changes in placebo or usual care. Numeric values for attribution counts are shown in eTable 1 in Supplement 2. Definitions and exemplars for each category are presented in the Table.
Figure 3.
Figure 3.. Effects of Pain Reprocessing Therapy (PRT) on Patients’ Attributions Regarding the Underlying Causes of Chronic Back Pain
Mind-brain attribution scores were computed by counting how many of the 3 attributions provided by participants were categorized as psychological, stress, or brain by coders masked to treatment condition and time point (range: 0-3, with higher scores indicating more mind or brain attributions). A, PRT produced large pre-to-posttreatment increases in mind-brain attribution scores relative to placebo and usual care. B, Within the PRT condition, pre-to-posttreatment increases in mind and brain attributions were significantly associated with decreases in pain intensity.
Figure 4.
Figure 4.. Scaling Analysis of Posttreatment Attributions Identifying Semantic Connections Underlying Free-Text Attributions
The first dimension ranged from primarily biomechanical words to primarily mind- or brain-related words. The location of each participant’s posttreatment attributions in the first dimension is shown, with 95% CIs around each condition’s mean location (top). Participants randomized to PRT vs placebo and usual care were significantly further toward the mind and brain end of the first dimension, and scores further toward the mind and brain end of the first dimension were associated with greater pain reduction.

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