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A randomized clinical trial of an integrated behavioral self-management intervention Simultaneously Targeting Obesity and Pain: the STOP trial

机译:同时针对肥胖和疼痛的综合行为自我管理干预措施的随机临床试验:STOP试验

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Background Obesity often occurs co-morbid with chronic, non-cancer pain. While behavioral treatments have proved effective for pain management and weight loss independently, integrated interventions are lacking. The study Simultaneously Targeting Obesity and Pain (STOP) is a prospective, pragmatic, randomized controlled trial that aims to determine whether overweight/obese individuals with chronic pain who are randomized to receive an integrated treatment Simultaneously Targeting Obesity and Pain (STOP) will show more weight loss and greater reduction in pain intensity over a 6-month period and greater maintenance at 12?months than those who receive standard care behavioral weight loss or standard care behavioral pain management. We hypothesize that individuals randomized to receive the STOP treatment will demonstrate improved weight loss, pain reduction, and maintenance compared to standard care treatment approaches. Methods/Design Adults aged?≥?18 with a body mass index?≥?25 and who report persistent pain (≥4 out of 0–10 for?>?6?months) will be recruited for treatment at the Health Behavior Research Lab at the University of the Sciences. After baseline assessments and goal setting, participants will be randomized to receive one of three treatments. Participants will receive eleven treatment sessions delivered during 1?hour, weekly individual meetings with a clinic therapist. Follow-up will occur at 3, 6 and 12-month time points; assessments will include measures of weight and pain intensity (primary outcomes). A mixed-method approach to evaluating study outcomes will include individual interviews with participants about their treatment experience. These interviews will be led by a research staffer who was not involved in study intervention or assessment using a semi-structured discussion guide. Discussion This study fills an important gap in intervention research, evaluating best-practices for behavioral management of a highly prevalent co-morbidity that has sub-optimal outcomes with currently-implemented approaches. STOP’s pragmatic focus builds upon treatments already in use in clinical practice. Should STOP be found efficacious in achieving the dual outcomes of pain management and weight loss, such an approach could be integrated into practice with minimal additional cost or training. Trial registration Clinical Trials.gov NCT02100995 Date of Registration: March 2014
机译:背景肥胖症通常与慢性非癌性疼痛并存。尽管行为疗法已被证明可有效地独立治疗疼痛和减轻体重,但仍缺乏综合干预措施。同时针对肥胖和疼痛的研究(STOP)是一项前瞻性,实用,随机对照试验,旨在确定是否有超重/肥胖的慢性疼痛患者被随机分配接受同时针对肥胖和疼痛的综合治疗(STOP)是否会显示更多信息。与接受标准护理行为减肥或标准护理行为疼痛管理的患者相比,他们在6个月内的体重减轻和疼痛强度的减轻程度更大,并且在12个月时的维持率更高。我们假设与标准护理治疗方法相比,随机接受STOP治疗的个体将表现出改善的体重减轻,疼痛减轻和维持能力。方法/设计年龄≥18岁且体重指数≥25且报告持续疼痛(≥6个月≥0≥4≥6个月)的成年人将被招募到健康行为研究实验室进行治疗在科学大学。经过基线评估和目标设定后,参与者将被随机分配接受三种治疗方法之一。参加者将在每周1个小时与临床治疗师进行的个人会议中接受十一次治疗会议。随访将在3、6和12个月的时间点进行;评估将包括体重和疼痛强度(主要结果)的量度。评估研究结果的混合方法将包括对参与者的治疗经历进行个别访谈。这些访谈将由一名研究人员领导,该研究人员不参与使用半结构化讨论指南进行的研究干预或评估。讨论本研究填补了干预研究中的一个重要空白,评估了高度流行的合并症的行为管理的最佳实践,该合并症在当前实施的方法中未达到最佳效果。 STOP的务实重点建立在临床实践中已经使用的治疗方法之上。如果发现STOP可以有效实现疼痛控制和减肥的双重效果,则可以将这种方法以最少的额外成本或培训整合到实践中。试验注册Clinical Trials.gov NCT02100995注册日期:2014年3月

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