首页> 外文期刊>BMC Public Health >Pilot study of a two-arm non-randomized controlled cluster trial of a psychosocial intervention to improve late life depression in socioeconomically deprived areas of S?o Paulo, Brazil (PROACTIVE): feasibility study of a psychosocial intervention for late life depression in S?o Paulo
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Pilot study of a two-arm non-randomized controlled cluster trial of a psychosocial intervention to improve late life depression in socioeconomically deprived areas of S?o Paulo, Brazil (PROACTIVE): feasibility study of a psychosocial intervention for late life depression in S?o Paulo

机译:在巴西圣保罗的社会经济匮乏地区进行心理社会干预以改善晚期生活抑郁症的两臂非随机对照聚类试验的先导研究(积极):在巴西南部的晚期抑郁症心理社会干预的可行性研究保罗

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Depression is a common and recurrent condition among older adults and is associated with poor quality of life and increased health care utilization and costs. The purpose of this pilot study was to assess the feasibility of delivering a psychosocial intervention targeting depression, and to develop the procedures to conduct a cluster randomized controlled trial among older adults registered with primary care clinics in poor neighbourhoods of S?o Paulo, Brazil. We conducted a pilot study of a two-arm cluster, non-randomized controlled trial. Two primary care clinics adhering to the Family Health Strategy were allocated to either the intervention or the control arm. In the control arm, patients received enhanced usual care consisting of staff training for improved recognition and management of depression. In the intervention arm, alongside the enhanced usual care, patients received a 17-week psychosocial intervention delivered by health workers assisted with an application installed in a tablet. We randomly selected 579 of 2020 older adults registered in the intervention clinic to participate in the study. Among these individuals, 353 were assessed for depression and 40 (11.0%) scored at least 10 on the PHQ-9 and were therefore invited to participate. The consent rate was 33/40 (82%) with a resulting yield of 33/579 (5.7%). In the control arm, we randomly selected 320 older adults among 1482 registered in the clinic, 223 were assessed for depression and 28 (12.6%) scored 10 or above on the PHQ-9. The consent rate was 25/28 (89%), with a resulting yield of 25/320 (7.8%). Of the 33 who consented in the intervention arm, 19 (59.4%) completed all sessions. The mean PHQ-9 at follow-up (approximately 30?weeks after inclusion) were 12.3 (SD?=?3.7) and 3.8 (SD?=?3.9) in the control and intervention arms, respectively. Follow-up rates were 92 and 94% in control and intervention arms, respectively. Identification and engagement of clinics, randomization, recruitment of individuals, measures, and baseline and follow-up assessments all proved to be feasible in primary care clinics in S?o Paulo, Brazil. Results support the development of a definitive cluster randomized controlled trial. This study was retrospectively registered with Registro Brasileiro de Ensaios Clínicos (ReBEC), number RBR-5nf6wd . Registered 06 August 2018.
机译:抑郁症是老年人中常见的复发性疾病,与生活质量差,医疗保健利用率和成本增加有关。这项初步研究的目的是评估针对抑郁症开展社会心理干预的可行性,并制定程序,在巴西圣保罗贫困地区的初级保健诊所注册的老年人中进行一项整群随机对照试验。我们对两臂集群,非随机对照试验进行了初步研究。遵循家庭健康战略的两家初级保健诊所被分配给干预或控制部门。在对照组中,患者接受了常规护理的加强,包括人员培训,以提高对抑郁症的认识和管理。在干预部门,除了加强常规护理外,患者还接受了由医务人员提供的为期17周的社会心理干预,并辅以安装在平板电脑上的应用程序。我们随机选择了2020年在干预诊所注册的579名老年人参加研究。在这些人中,有353名被评估为抑郁症,有40名(11.0%)在PHQ-9上得分至少10分,因此被邀请参加。同意率为33/40(82%),结果收益率为33/579(5.7%)。在对照组中,我们从诊所中登记的1482名患者中随机选择了320名老年人,对223名抑郁症进行了评估,有28名(12.6%)在PHQ-9上得分为10分或更高。同意率为25/28(89%),结果收益率为25/320(7.8%)。在接受干预的33位患者中,有19位(59.4%)完成了所有环节。随访(包括入组后约30周)的平均PHQ-9在对照组和干预组分别为12.3(SD≥3.7)和3.8(SD≥3.9)。对照组和干预组的随访率分别为92%和94%。在巴西圣保罗的初级保健诊所,诊所的确定和参与,随机化,人员的招募,措施以及基线和后续评估都被证明是可行的。结果支持确定性整群随机对照试验的发展。这项研究已在巴西利亚登记局(ReBEC)登记,编号为RBR-5nf6wd。 2018年8月6日注册。

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