首页> 外文期刊>Trials >The STRATOB study: design of a randomized controlled clinical trial of Cognitive Behavioral Therapy and Brief Strategic Therapy with telecare in patients with obesity and binge-eating disorder referred to residential nutritional rehabilitation
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The STRATOB study: design of a randomized controlled clinical trial of Cognitive Behavioral Therapy and Brief Strategic Therapy with telecare in patients with obesity and binge-eating disorder referred to residential nutritional rehabilitation

机译:STRATOB研究:肥胖和暴饮暴食患者的认知行为疗法和简短策略疗法与远程护理的随机对照临床试验设计,该研究被称为居民营养康复

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Background Overweight and obesity are linked with Binge Eating Disorder (BED). Effective interventions to significantly reduce weight, maintain weight loss and manage associated pathologies like BED are tipically combined treatment options (dietetic, nutritional, physical, behavioral, cognitive-behavioral, pharmacological, surgical). Significant difficulties with regard to availability, costs, treatment adherence and long-term efficacy are present. Particularly Cognitive Behavioral Therapy (CBT) is the therapeutic approach indicated both in in-patient and in out-patient settings for BED. In recent years systemic and systemic-strategic psychotherapies have been implemented to treat patients with obesity and BED involved in familiar problems. Particularly a brief protocol for the systemic-strategic treatment of BED, using overall the strategic dialogue, has been recently developed. Moreover telemedicine, a new promising low cost method, has been used for obesity with BED in out-patient settings in order to avoid relapse after the in-patient step of treatment and to keep on a continuity of care with the involvement of the same clinical in-patient team. Methods The comparison between CBT and Brief Strategic Therapy (BST) will be assessed in a two-arm randomized controlled clinical trial. Due to the novelty of the application of BST in BED treatment (no other RCTs including BST have been carried out), a pilot study will be carried out before conducting a large scale randomized controlled clinical trial (RCT). Both CBT and BST group will follow an in-hospital treatment (diet, physical activity, dietitian counseling, 8 psychological sessions) plus 8 out-patient telephone-based sessions of psychological support and monitoring with the same in-patient psychotherapists. Primary outcome measure of the randomized trial will be the change in the Global Index of the Outcome Questionnaire (OQ-45.2). Secondary outcome measures will be the percentage of BED patients remitted considering the number of weekly binge episodes and the weight loss. Data will be collected at baseline, at discharge from the hospital (c.a. 1 month after) and after 6-12-24 months from the end of the in-hospital treatment. Data at follow-up time points will be collected through tele-sessions. Discussion The STRATOB (Systemic and STRATegic psychotherapy for OBesity), a comprehensive two-phase stepped down program enhanced by telepsychology for the medium-term treatment of obese people with BED seeking intervention for weight loss, will shed light about the comparison of the effectiveness of the BST with the gold standard CBT and about the continuity of care at home using a low-level of telecare (mobile phones). Trial registration ClinicalTrials.gov Identifier: NCT01096251
机译:背景超重和肥胖与暴食症(BED)有关。有效的干预措施可以显着减轻体重,保持体重减轻并管理相关的疾病(如BED),是最终的综合治疗选择(饮食,营养,身体,行为,认知行为,药理,外科)。在可用性,成本,治疗依从性和长期疗效方面存在重大困难。特别是认知行为疗法(CBT)是在住院和门诊就诊BED的治疗方法。近年来,已经实施了全身性和系统性策略性心理治疗,以治疗肥胖和患有常见问题的BED患者。特别是,最近已开发出使用总体战略对话进行BED系统策略治疗的简短协议。此外,远程医疗是一种新的有前途的低成本方法,已被用于门诊患者的BED肥胖症,以避免在住院治疗后复发,并在同一临床试验的参与下保持护理的连续性住院团队。方法将在两臂随机对照临床试验中评估CBT与简要策略疗法(BST)之间的比较。由于BST在BED治疗中的新颖性(尚未进行包括BST的其他RCT),因此在进行大规模随机对照临床试验(RCT)之前将进行先导研究。 CBT和BST组将接受住院治疗(饮食,体育锻炼,营养师咨询,8次心理治疗),以及8次基于电话的心理支持和监护,并由同一名住院心理治疗师进行监测。随机试验的主要结局指标是结果问卷全球指数(OQ-45.2)的变化。次要结果衡量指标是考虑到每周暴饮暴食发作的次数和体重减轻后,BED患者的缓解百分比。数据将在基线,医院出院时(约1个月后)以及住院治疗结束后6-12-24个月后收集。后续时间点的数据将通过远程会议收集。讨论STRATOB(针对肥胖症的全身性和STRATegic心理治疗)是一项综合的两阶段逐步降低计划,通过远程心理增强功能,可对寻求减肥干预的BED肥胖患者进行中期治疗,这将为人们比较具有黄金标准CBT的BST,以及使用低水平远程护理(移动电话)在家中护理的连续性。试验注册ClinicalTrials.gov标识符:NCT01096251

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