Pilot study of feasibility, acceptability, and changes in clinical outcomes following a brief trauma-focused intervention for chronic pain.
case_series · Level IV
Where this comes from
- Record sourced from PubMed, PMID 42350064.
- Also identified by DOI 10.1136/rapm-2026-107849.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Trauma exposure is prevalent among individuals with chronic pain and is associated with poorer pain-related outcomes. Brief, scalable interventions that target overlapping trauma-pain processes are needed. This single-arm pilot study evaluated feasibility, acceptability, and changes in clinical outcomes following Stress, Trauma, and Emotional Processing for Pain (STEPP), a brief modified version of emotional awareness and expression therapy. Adults (N=42) with mixed-etiology chronic pain and trauma exposure were enrolled. STEPP was delivered remotely over three weekly 1-hour individual sessions. Participants completed questionnaires at baseline, post-treatment, and 1-month, and 3-month follow-up. Feasibility benchmarks (≥70%) were prespecified for recruitment, treatment, and follow-up completion. Acceptability was assessed using the Treatment Helpfulness Questionnaire (THQ; -5 to 5) and Credibility and Expectancy Questionnaire (content credibility and expected benefit; 3-27). Linear mixed models and Hedges' g effect sizes examined changes in pain intensity (0-10) and interference with functioning (0-100), post-traumatic stress disorder symptoms (PTSD; 0-80), pain catastrophizing (concerns about pain; 0-52), and kinesiophobia (fear of movement; 17-68). All feasibility benchmarks were met. 93% of eligible participants enrolled, 90% of enrolled participants initiated treatment, and 97% initiators completed treatment. Among completers, follow-up completion was 100% at post-treatment and 97% at 1 and 3 months. THQ ratings were high and met benchmarks (post M=4.0±1.2; 1-month M=3.9±1.2; 3-month M=3.8±1.3). Credibility ratings met benchmarks, whereas expectancy ratings did not. Significant improvements were observed from baseline to post-treatment: pain intensity (mean change=-0.64, SE=0.23, 95% CI -1.11 to -0.18), pain interference (-3.34, SE=0.84, 95% CI -5.00 to -1.68), PTSD (-5.60, SE=1.53, 95% CI -8.64 to -2.57), pain catastrophizing (-6.69, SE=1.34, 95% CI -9.34 to -4.03), and kinesiophobia (-5.78, SE=1.21, 95% CI -8.19 to -3.37); changes were maintained through 3 months. Effect sizes were small for pain intensity and moderate-to-large for all other outcomes. STEPP demonstrated feasibility and acceptability, with promising improvements in pain-related and trauma-related outcomes. Randomized controlled trials are needed to establish efficacy.