This research is studying whether a Zoom-based behavioral intervention may have an impact as a treatment for Veterans with Chronic Low Back Pain (CLBP). The study will examine: * The acceptability of the Brief Pain Reprocessing Therapy (BPRT) intervention * The feasibility of the BPRT intervention * The safety of the BPRT intervention
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Acceptability of and satisfaction with treatment base on the mean scores on the Treatment Evaluation Inventory (TEI-SF) assessed at T5 (approximately day 35)
Timeframe: Approximately day 35 (post treatment)
Feasibility will be accessed by participant adherence
Timeframe: Up to approximately day 35 (post treatment)
Feasibility will be accessed by feedback from the Qualitative Interviews
Timeframe: Approximately day 35 (post treatment)
Safety will be assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS 29) pain intensity
Timeframe: Baseline, up to day 35 post treatment
Safety will be assessed by the PROMIS Depression scale
Timeframe: Baseline, up to day 35 post treatment
Safety will be assessed by the PROMIS Anxiety scale
Timeframe: Baseline, up to day 35 post treatment
Safety will be assessed by the Patient Global Impression of Change (PGIC)
Timeframe: Baseline, up to day 35 post treatment
Safety assessed by the number of Adverse events and Serious adverse events T6 (Day 60) - T9 (Day 210)
Timeframe: T6 (Day 60) - T9 (Day 210)