Instituto de Psiquiatria, Hospital das Clinicas, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, Brazil; Departamento de Psiquiatria, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, Brazil.
Departamento de Psiquiatria, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, Brazil.
Lancet Healthy Longev. 2022 Oct;3(10):e690-e702. doi: 10.1016/S2666-7568(22)00194-5.
There is an urgent need to reduce the burden of depression among older adults in low-income and middle-income countries (LMICs). We aimed to evaluate the efficacy of a task-shared, collaborative care psychosocial intervention for improving recovery from depression in older adults in Brazil.
PROACTIVE was a pragmatic, two-arm, parallel-group, cluster-randomised controlled trial conducted in Guarulhos, Brazil. Primary care clinics (clusters) were stratified by educational level and randomly allocated (1:1) to either enhanced usual care alone (control group) or to enhanced usual care plus the psychosocial intervention (intervention group), which involved a 17-week psychosocial programme based on psychoeducation and behavioural activation approaches. Individuals approached for the initial screening assessment were selected randomly from a list of individuals provided by the Health Secretariat of Guarulhos. Face-to-face baseline assessments were conducted among adults aged 60 years or older registered with one of the primary care clinics and identified with clinically significant depressive symptomatology (9-item Patient Health Questionnaire [PHQ-9] score ≥10). Community health workers delivered the programme through home sessions, supported by a dedicated tablet application. Masking of clinic staff and community health workers who delivered the intervention was not feasible; however, research assistants conducting recruitment and follow-up assessments were masked to trial allocation. The primary outcome was recovery from depression (PHQ-9 score <10) at 8-month follow-up. All primary analyses were performed by intention to treat with imputed data. Adaptations to the protocol were made due to the COVID-19 pandemic; recruitment and intervention home sessions were stopped, and follow-up assessments were conducted by telephone. This trial is registered with the ISRCTN registry, ISRCTN57805470.
We identified 24 primary care clinics in Guarulhos that were willing to participate, of which 20 were randomly allocated to either the control group (ten [50%] clusters) or to the intervention group (ten [50%] clusters). The four remaining eligible clusters were kept as reserves. Between May 23, 2019, and Feb 21, 2020, 8146 individuals were assessed for eligibility, of whom 715 (8·8%) participants were recruited: 355 (49·7%) in the control group and 360 (50·3%) in the intervention group. 284 (80·0%) participants in the control group and 253 (70·3%) in the intervention group completed follow-up at 8 months. At 8-month follow-up, 158 (62·5%) participants in the intervention group showed recovery from depression (PHQ-9 score <10) compared with 125 (44·0%) in the control group (adjusted odds ratio 2·16 [95% CI 1·47-3·18]; p<0·0001). These findings were maintained in the complete case analysis. No adverse events related to the intervention were observed.
Although the COVID-19 pandemic altered delivery of the intervention, the low-intensity psychosocial intervention delivered mainly by non-mental health professionals was highly efficacious in improving recovery from depression in older adults in Brazil. Our results support a low-resource intervention that could be useful to reduce the treatment gap for depression among older people in other LMICs.
São Paulo Research Foundation and Joint Global Health Trials (UK Department for International Development, Medical Research Council, and the Wellcome Trust).
在中低收入国家(LMICs),降低老年人抑郁负担迫在眉睫。我们旨在评估一种任务分担、协作式心理社会干预措施在改善巴西老年人抑郁康复方面的疗效。
PROACTIVE 是一项在巴西瓜鲁柳斯进行的务实、两臂、平行组、聚类随机对照试验。初级保健诊所(集群)按教育水平分层,并随机(1:1)分配到强化常规护理(对照组)或强化常规护理加心理社会干预(干预组),干预组包括基于心理教育和行为激活方法的为期 17 周的心理社会方案。从瓜鲁柳斯卫生秘书处提供的个人名单中随机选择符合初始筛选评估条件的个人。对登记在一家初级保健诊所并具有临床显著抑郁症状(9 项患者健康问卷 [PHQ-9] 得分≥10)的 60 岁及以上成年人进行面对面基线评估。社区卫生工作者通过家庭会议提供该方案,由专用平板电脑应用程序提供支持。无法对诊所工作人员和提供干预的社区卫生工作者进行掩蔽;但是,进行招募和随访评估的研究助理对试验分配进行了掩蔽。主要结局是在 8 个月随访时从抑郁中恢复(PHQ-9 得分<10)。所有主要分析均采用意向治疗和插补数据进行。由于 COVID-19 大流行,对方案进行了调整;停止了招募和干预家庭会议,并通过电话进行了随访评估。本试验在 ISRCTN 注册处注册,ISRCTN57805470。
我们确定了 24 家愿意参与的瓜鲁柳斯初级保健诊所,其中 20 家被随机分配到对照组(10 个[50%]集群)或干预组(10 个[50%]集群)。其余四个符合条件的集群被保留为储备。2019 年 5 月 23 日至 2020 年 2 月 21 日,对 8146 名符合条件的人进行了评估,其中 715 名(8.8%)参与者被招募:对照组 355 名(49.7%),干预组 360 名(50.3%)。对照组有 284 名(80.0%)参与者和干预组有 253 名(70.3%)参与者在 8 个月时完成了随访。在 8 个月的随访中,与对照组的 125 名(44.0%)相比,干预组有 158 名(62.5%)参与者从抑郁中恢复(PHQ-9 得分<10)(调整后的优势比 2.16[95%CI 1.47-3.18];p<0.0001)。这些发现在完全案例分析中得到了维持。未观察到与干预相关的不良事件。
尽管 COVID-19 大流行改变了干预措施的实施方式,但主要由非心理健康专业人员提供的低强度心理社会干预措施在改善巴西老年人抑郁康复方面非常有效。我们的研究结果支持一种低资源的干预措施,该措施可能有助于减少其他中低收入国家老年人的抑郁症治疗差距。
圣保罗研究基金会和全球联合健康试验(英国国际发展部、医学研究理事会和惠康信托基金会)。