San Francisco Department of Veterans Affairs (VA) Healthcare System.
Department of Psychiatry, University of California, San Francisco.
Clin J Pain. 2024 Nov 1;40(11):655-664. doi: 10.1097/AJP.0000000000001243.
This study compared clinical pain outcomes between patients in a pain treatment program that was conducted in-person, compared with a virtual program.
In-person (N=127) and virtual (N=101) pain treatment programs were compared based on patient-reported, practitioner-collected, and medical record data. The patients were measured at baseline and post-treatment (week 12 for In-Person and week 8 for Virtual patients). We employed the last observation carried forward (LOCF) to handle missing data.
Both the In-Person and Virtual groups were similar in regard to all baseline outcomes, except the In-person group having significantly more co-morbidities at baseline, with particularly more cases of mental, behavioral, or neurodevelopmental diseases. Both groups demonstrated significant improvements in the pain-related measurements of pain interference and pain catastrophizing thoughts, but neither group displayed a change in average pain across treatment. Further, both groups improved significantly on emotional well-being scores, but not on physical functioning scores. No significant differences existed between groups on outcomes, except for pain catastrophizing, which was higher in the Virtual group at both time points. The Virtual group had lower rates of dropouts compared with In-Person, while the In-Person group had a larger proportion reach a clinically meaningful change in pain-related outcomes, defined as a >30% improvement.
While some changes were unique to the In-Person program, overall, patients in the Virtual program achieved similar treatment outcomes, suggesting that it can successfully treat Veterans seeking pain management, with less need for in-person facilities for both patients and clinicians.
本研究比较了在面对面和虚拟疼痛治疗项目中患者的临床疼痛结果。
根据患者报告、医生收集和病历数据,比较了面对面(N=127)和虚拟(N=101)疼痛治疗计划。患者在基线和治疗后(面对面组为第 12 周,虚拟组为第 8 周)进行测量。我们采用最后观察值结转(LOCF)处理缺失数据。
面对面和虚拟组在所有基线结果方面都相似,除了面对面组在基线时合并症明显更多,特别是精神、行为或神经发育疾病的病例更多。两组在与疼痛相关的疼痛干扰和疼痛灾难化思维测量方面均显示出显著改善,但两组在治疗过程中平均疼痛均无变化。此外,两组在情绪健康评分方面均有显著改善,但在身体功能评分方面没有改善。除了疼痛灾难化,两组在结果上没有显著差异,而疼痛灾难化在两个时间点都更高。虚拟组的辍学率低于面对面组,而面对面组有更大比例的患者在疼痛相关结局方面达到临床有意义的改善,定义为疼痛改善>30%。
虽然一些变化是面对面计划独有的,但总体而言,虚拟计划中的患者取得了相似的治疗结果,这表明它可以成功治疗寻求疼痛管理的退伍军人,患者和临床医生对面对面设施的需求减少。