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Cognitive behavioral intervention via a smartphone app for non-professional caregivers with depressive symptoms: study protocol for a randomized controlled trial

机译:通过智能手机应用程序对非专业护理人员具有抑郁症状的认知行为干预:随机对照试验的研究方案

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Although major depression is a frequent disorder in non-professional caregivers and there are effective psychological interventions to prevent it, caregivers have difficulty accessing them. Interventions for depression applied through an app could improve accessibility; yet, to date, adherence to such interventions has been low. The objectives of this study are to (1) evaluate the efficacy of a cognitive behavioral depression prevention intervention administered through a smartphone app with and without telephone conference calls, (2) analyze the mediators of the change in the incidence of depression and depressive symptoms, and (3) assess adherence and satisfaction with the interventions. A randomized controlled clinical trial will be conducted. Caregivers with elevated symptoms will be randomly assigned to a cognitive behavioral intervention administered by a smartphone app (CBIA) group, a CBIA plus telephone conference calls (TCCs) group (CBIA + TCC), or an attention control group. Each condition will consist of approximately 58 participants. Both interventions will be administered in five modules through a smartphone app and the CBIA + TCC group will receive additional TCCs in group format (four sessions of 30?min each). Trained blind assessors will conduct pre-treatment, post-treatment and follow-up assessments at 1, 3, 6, and 12?months. This study will provide evidence of the efficacy of a cognitive behavioral intervention to prevent depression in caregivers with elevated depressive symptoms administered through a smartphone app and the impact of feedback applied through conference calls to increase program adherence and efficacy. If the results were favorable, it would mean that we have developed a more effective, accessible, and clinically useful preventive depression intervention than the currently available ones for many present and future caregivers. ClinicalTrials.gov: NCT03110991 . Registered 5 April 2017.
机译:虽然重大抑郁症是非专业护理人员的频繁紊乱,但有有效的心理干预措施,以防止它,看护人难以进入它们。通过应用程序应用的抑郁症的干预可以改善可访问性;然而,迄今为止,依从这种干预措施已经很低。本研究的目标是(1)评估通过智能手机应用程序管理的认知行为抑郁防止干预的疗效,而无电话会议电话,(2)分析抑郁症发病率发生率的变化的调解员, (3)与干预措施评估依从性和满意度。将进行随机对照临床试验。具有升高症状的护理人员将被随机分配给由智能手机应用程序(CBIA)组,CBIA Plus电话会议(TCC)组(CBIA + TCC)或注意力控制组管理的认知行为干预。每个条件都包括大约58名参与者。两种干预措施都将通过智能手机应用程序在五个模块中管理,CBIA + TCC组将以组格式收到额外的TCC(每个30个课程,每次30个)。培训的盲人评估员将在1,3,6和12个月内进行预处理,后处理和后续评估。本研究将提供认知行为干预的效果,以防止通过智能手机应用程序管理的抑郁症状和通过会议呼叫的反馈的影响来增加计划依从性和疗效的抑郁症患者抑郁症的疗效证据。如果结果有利,这将意味着我们已经开发出比目前和未来护理人员的目前可用的更有效,可进入和临床有用的预防性抑郁症干预。 ClinicalTrials.gov:NCT03110991。注册2017年4月5日。

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