Center for Care Delivery and Outcomes Research, Minneapolis Veterans Affairs Health Care System (VAHCS), Minneapolis, MN 55417, United States.
University of Minnesota Medical School, Minneapolis, MN 55455, United States.
Pain Med. 2024 Nov 1;25(Supplement_1):S68-S76. doi: 10.1093/pm/pnae056.
Although mindfulness-based interventions (MBIs) are widely used in clinical and nonclinical settings, there has been little systematic study of their potential risks. To address this gap, we examined differences in psychological and physical worsening among participants in the usual care and intervention conditions of a 3-group, randomized pragmatic trial (Learning to Apply Mindfulness to Pain [LAMP]) that tested the effectiveness of 2 approaches to delivering MBIs to patients with chronic pain.
The sample consisted of 374 male and 334 female patients with chronic pain enrolled in the LAMP trial who completed a 10-week follow-up survey, 61% of whom had a mental health diagnosis. Psychological and physical worsening was assessed by a checklist asking whether participants experienced specific symptoms since beginning the study. We used multivariable logistic regression models with imputed data to determine whether predicted probabilities of increased symptoms differed between usual care and the 2 MBIs.
Participants in usual care were more likely to report experiencing increased psychological and physical worsening than were those in the MBIs, including an increase in disturbing memories; sadness, anxiousness, and fatigue; isolation and loneliness; and feeling more upset than usual when something reminded them of the past.
MBIs do not appear to cause harm, in terms of increased symptoms, for this population of patients with chronic pain and high levels of mental health comorbidities.
Preregistration with an analysis plan at www.ClinicalTrials.gov: NCT04526158. Patient enrollment began December 4, 2020.
尽管基于正念的干预(MBIs)在临床和非临床环境中被广泛应用,但对其潜在风险的系统研究却很少。为了弥补这一空白,我们研究了在一项 3 组随机实用试验(学习将正念应用于疼痛[LAMP])中,接受常规护理和干预条件的参与者在心理和身体恶化方面的差异,该试验测试了两种向慢性疼痛患者提供 MBIs 的方法的有效性。
该样本包括参加 LAMP 试验的 374 名男性和 334 名女性慢性疼痛患者,他们完成了 10 周的随访调查,其中 61%的人有心理健康诊断。通过询问参与者自研究开始以来是否出现特定症状的清单来评估心理和身体恶化情况。我们使用带有插补数据的多变量逻辑回归模型来确定常规护理和 2 种 MBIs 之间是否存在症状增加的预测概率差异。
与接受 MBIs 的参与者相比,接受常规护理的参与者更有可能报告经历心理和身体恶化,包括干扰记忆增加;悲伤、焦虑和疲劳;孤立和孤独;以及当某事使他们想起过去时,感到比平时更不安。
对于患有慢性疼痛和心理健康共病率较高的这一人群来说,MBIs 似乎不会导致症状加重,从而造成伤害。
在 www.ClinicalTrials.gov 上进行预注册并附有分析计划:NCT04526158。患者招募于 2020 年 12 月 4 日开始。