...
首页> 外文期刊>Trials >Task sharing of a psychological intervention for maternal depression in Khayelitsha, South Africa: study protocol for a randomized controlled trial
【24h】

Task sharing of a psychological intervention for maternal depression in Khayelitsha, South Africa: study protocol for a randomized controlled trial

机译:南非Khayelitsha产妇抑郁症心理干预的任务共享:一项随机对照试验的研究方案

获取原文
           

摘要

Background Maternal depression carries a major public health burden for mothers and their infants, yet there is a substantial treatment gap for this condition in low-resourced regions such as sub-Saharan Africa. To address this treatment gap, the strategy of “task sharing” has been proposed, involving the delivery of interventions by non-specialist health workers trained and supervised by specialists in routine healthcare delivery systems. Several psychological interventions have shown benefit in treating maternal depression, but few have been rigorously evaluated using a task sharing approach. The proposed trial will be the first randomised controlled trial (RCT) evaluating a task sharing model of delivering care for women with maternal depression in sub-Saharan Africa. The objective of this RCT is to determine the effectiveness and cost-effectiveness of a task sharing counseling intervention for maternal depression in South Africa. Methods/Design The study is an individual-level two-arm RCT. A total of 420 depressed pregnant women will be recruited from two ante-natal clinics in a low-income township area of Cape Town, using the Edinburgh Postnatal Depression Scale to screen for depression; 210 women will be randomly allocated to each of the intervention and control arms. The intervention group will be given six sessions of basic counseling over a period of 3 to 4?months, provided by trained community health workers (CHW)s. The control group will receive three monthly phone calls from a CHW trained to conduct phone calls but not basic counseling. The primary outcome measure is the 17-Item Hamilton Depression Rating Scale (HDRS-17). The outcome measures will be applied at the baseline assessment, and at three follow-up points: 1?month before delivery, and 3 and 12?months after delivery. The primary analysis will be by intention-to-treat and secondary analyses will be on a per protocol population. The primary outcome measure will be analyzed using linear regression adjusting for baseline symptom severity measured using the HDRS-17. Discussion The findings of this trial can provide policy makers with evidence regarding the effectiveness and cost-effectiveness of structured psychological interventions for maternal depression delivered by appropriately trained and supervised non-specialist CHWs in sub-Saharan Africa. Trial registration Clinical Trials (ClinicalTrials.gov): NCT01977326 , registered on 24/10/2013; Pan African Clinical Trials Registry ( http://www.pactr.org webcite ): PACTR201403000676264 , registered on 11/10/2013.
机译:背景技术产妇抑郁症对母亲及其婴儿造成重大的公共卫生负担,但是在资源贫乏的地区(如撒哈拉以南非洲),这种情况存在巨大的治疗差距。为了解决这种治疗差距,已经提出了“任务共享”的策略,其中涉及由经过常规医疗服务提供系统的专家培训和监督的非专职医疗人员提供的干预措施。几种心理干预措施已显示出对治疗孕妇抑郁症的益处,但很少采用任务分担方法进行严格评估。拟议的试验将是第一个评估为撒哈拉以南非洲产妇抑郁症妇女提供护理的任务分担模型的随机对照试验(RCT)。该RCT的目的是确定针对南非孕产妇抑郁症的任务共享咨询干预措施的有效性和成本效益。方法/设计该研究是个人水平的两臂RCT。在爱丁堡的产后抑郁量表中,将在开普敦低收入地区的两家产前诊所招募总共420名抑郁症孕妇,以筛查抑郁症;每个干预和控制部门将随机分配210名妇女。干预小组将在3到4个月内接受由经过培训的社区卫生工作者(CHW)提供的六次基本咨询。对照组将从经过培训的CHW每月接到三个电话,但不能接受基本咨询。主要结果指标是17项汉密尔顿抑郁等级量表(HDRS-17)。结果测量将在基线评估和三个随访点上应用:分娩前1个月,分娩后3个月和12个月。主要分析将通过意向治疗,次要分析将在每个方案人群中进行。主要结果指标将使用线性回归分析,以校正使用HDRS-17测得的基线症状严重程度。讨论该试验的结果可为政策制定者提供证据,说明撒哈拉以南非洲由经过适当培训和监督的非专科CHW进行的针对产妇抑郁的结构性心理干预的有效性和成本效益。试验注册临床试验(ClinicalTrials.gov):NCT01977326,于2013年10月24日注册;泛非临床试验注册中心(http://www.pactr.org webcite):PACTR201403000676264,注册时间为11/10/2013。

相似文献

  • 外文文献
  • 中文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号