Pain Research, Informatics, Multimorbidities, and Education (PRIME) Center, West Haven, CT, USA.
Yale School of Medicine, Yale University, New Haven, CT, USA.
J Behav Med. 2024 Dec;47(6):994-1001. doi: 10.1007/s10865-024-00511-4. Epub 2024 Aug 14.
This analysis was part of the Pain and Smoking Study (PASS), a randomized trial of a cognitive behavioral intervention (CBI) for Veterans with chronic pain who smoke. The objective of this study was to examine factors associated with participation in the walking component of the intervention. Demographics and clinical characteristics were obtained at baseline. Completion of two or more CBI counseling sessions was required to be included in analyses. Average daily step counts obtained via pedometer in the prior week were recorded in up to three telephone counseling sessions. Participants were then categorized as "sedentary" (≤ 4999 daily steps) or "not sedentary" (≥ 5000 daily steps). Multivariable logistic regression was used to model variance in activity categorization. Overall, 91.0% of participants were men, 70.5% were white, mean age was 58.4 years, mean BMI was 28.6, median pack years was 20.5, and 43.8% were depressed. Veterans reported moderate pain intensity (4.9/10) and pain interference (5.4/10). Pain locations included: lower extremity (67.4%), back (53.4%) and upper extremity (28.1%). Median daily steps were 2491 [IQR: 1720-3550] (sedentary) (n = 65), 7307 [IQR: 5952-8533] (not sedentary) (n = 24), and 3196 [IQR: 2237-5067] (overall) (n = 89). Veterans with older age (odds ratio (OR): 1.10, 95% confidence interval (CI): 1.04, 1.17) and presence of LE pain (OR: 5.98, 95% CI: 1.82, 19.65) had increased odds of being "sedentary." Integrated smoking cessation and chronic pain self-management interventions that include a walking component may need to consider the impact of age and pain location on participation.Trial registration: The trial is registered at www.ClinicalTrials.gov (NCT02971137). First posted on November 22, 2016.
本分析是一项针对患有慢性疼痛且吸烟的退伍军人的认知行为干预(CBI)的随机试验——疼痛和吸烟研究(PASS)的一部分。本研究的目的是探讨与干预步行部分参与相关的因素。在基线时获得人口统计学和临床特征。完成两次或更多次 CBI 咨询课程是进行分析的必要条件。在多达三次电话咨询中记录了前一周通过计步器获得的平均每日步数。然后将参与者分为“久坐”(≤4999 步/天)或“非久坐”(≥5000 步/天)。多变量逻辑回归用于对活动分类的方差建模。总体而言,91.0%的参与者为男性,70.5%为白人,平均年龄为 58.4 岁,平均 BMI 为 28.6,中位数吸烟年数为 20.5,43.8%患有抑郁症。退伍军人报告中度疼痛强度(4.9/10)和疼痛干扰(5.4/10)。疼痛部位包括:下肢(67.4%)、背部(53.4%)和上肢(28.1%)。中位数每日步数为 2491 [IQR:1720-3550](久坐)(n=65),7307 [IQR:5952-8533](非久坐)(n=24),3196 [IQR:2237-5067](总体)(n=89)。年龄较大的退伍军人(优势比(OR):1.10,95%置信区间(CI):1.04,1.17)和下肢疼痛(OR:5.98,95%CI:1.82,19.65)的退伍军人更有可能“久坐”。包含步行部分的综合戒烟和慢性疼痛自我管理干预措施可能需要考虑年龄和疼痛部位对参与的影响。
该试验在 www.ClinicalTrials.gov 上注册(NCT02971137)。首次于 2016 年 11 月 22 日发布。