Expanding mental health counselling from primary care to reach at-risk youth (Expanding MINDS-Y).

将心理健康咨询从初级保健扩展到高危青少年（Expanding MINDS-Y）。

• 批准号: MR/R018464/1
• 负责人: Bronwyn Myers
• 金额: $ 19.24万
• 依托单位: South African Medical Research Council
• 依托单位国家: 英国
• 项目类别: Research Grant
• 财政年份: 2018
• 资助国家: 英国
• 起止时间: 2018 至 无数据
• 项目状态: 已结题
• 来源: https://gtr.ukri.org/projects?ref=MR%2FR018464%2F1
• 关键词: Expanding; mental; health; counselling; primary

Ensuring youth (aged 15-24) who are at high risk for common mental disorders like depression and hazardous alcohol use have access to mental health counselling could improve their emotional well-being and prevent injuries, the acquisition of communicable diseases such as HIV, and the onset of non-communicable diseases (NCDs). Like many low- and middle-income countries (LMICs), South Africa (SA) faces the challenge of how to reduce the high prevalence and impact of communicable diseases and NCDs, including mental disorders where limited services are available. Common mental disorders among youth are important to address to prevent these future physical health problems. Yet, the mental health treatment gap in SA is large, particularly for youth. Failure to reach 15-24 year olds is a major service gap as this is often the age of onset for common mental disorders. Service planners recognise that they need to expand the coverage of mental health counselling to include at-risk youth. However, a lack of information about where to situate mental health counselling services, who should be delivering these services, and how to format services to ensure acceptability to and utilisation by at-risk youth has hampered the expansion of available services to this key population. The expansion of mental health counselling to at-risk youth also has been delayed by a lack of youth-oriented counselling programmes that are acceptable to and effective for improving the mental health of at-risk youth. The goal of this study is to address this knowledge gap by providing information on youth preferences for mental health counselling services, adapting an adult-oriented programme to meet the needs of youth; and testing the feasibility of recruiting youth and initial outcomes of this adapted counselling programme on mental health outcomes. Through this study, we hope to obtain information that can be directly useful to health planners for the design and development of youth-friendly mental health counselling services and have a feasible, youth-friendly counselling programme that shows promise for reducing both depression and hazardous alcohol use among at-risk youth. Findings from this study are likely to be highly relevant for use in other LMICs given similarities between the burden of disease, treatment populations, and profile of risk behaviours among youth in SA and other LMICs.The study will comprise three phases. In the first phase, we will conduct in-depth interviews with service providers, at-risk youth, and their caregivers to assess barriers to youth participation in mental health counselling and to identify youth preferences for where and how services should be delivered (Aim 1). Findings from this phase will be used to initially adapt our proposed programme to address these barriers and ensure acceptability. In Aim 2, we will demonstrate this adapted intervention in focus groups with at-risk youth in order to obtain information on how the intervention content, structure and layout should be adapted to meet the needs of youth. In Phase 3, we will test the feasibility of recruiting at risk youth to participate in the adapted intervention and the initial effect of the adapted intervention on depression and hazardous alcohol use. We will recruit 100 at-risk youth from impoverished community settings and we will randomize them to receive the intervention or be in a control group. We will assess the effect of the intervention on depression and alcohol use three months after study enrolment. Once the three month assessment has been completed, participants in the control group will be offered the counselling intervention. Findings from this phase will be used to initially evaluate the feasibility and effect of the intervention (Aims 3-4). If the outcomes are promising, findings will also be used to inform the design of a large trial to assess the effectiveness and cost-effectiveness of this intervention.

确保抑郁症和危险酒精使用等常见精神障碍的高风险青年（15 - 24岁）获得心理健康咨询，可以改善他们的情绪健康，预防伤害，预防艾滋病毒等传染病的感染和非传染性疾病的发生。与许多低收入和中等收入国家一样，南非（SA）面临着如何降低传染病和非传染性疾病（包括服务有限的精神障碍）的高流行率和影响的挑战。青年人中常见的精神障碍是重要的，以防止这些未来的身体健康问题。然而，SA的心理健康治疗差距很大，特别是对年轻人来说。未能接触到15 - 24岁的人是一个主要的服务差距，因为这往往是常见精神障碍的发病年龄。服务规划者认识到，他们需要扩大心理健康咨询的覆盖面，将高危青年包括在内。然而，由于缺乏关于在何处提供心理健康咨询服务、应由谁提供这些服务以及如何安排服务以确保高危青年接受和利用这些服务的信息，阻碍了向这一关键人群扩大现有服务。向问题青年提供心理健康咨询的工作也因缺乏为问题青年所接受并能有效改善其心理健康的面向青年的咨询方案而受到拖延。这项研究的目标是解决这一知识差距，提供信息，青年心理健康咨询服务的偏好，调整面向成年人的方案，以满足青年的需求，并测试招聘青年的可行性和心理健康结果的这一调整后的咨询方案的初步成果。通过这项研究，我们希望获得的信息，可以直接有用的卫生规划人员的设计和发展的青年友好的心理健康咨询服务，并有一个可行的，青年友好的咨询方案，显示减少抑郁症和危险的酒精使用的风险青年。鉴于南非和其他中低收入国家青年的疾病负担、治疗人群和风险行为概况之间的相似性，这项研究的结果可能与其他中低收入国家的使用高度相关。在第一阶段，我们会与服务提供者、边缘青少年及其照顾者进行深入访谈，以评估青少年参与精神健康辅导的障碍，并确定青少年对服务提供地点和方式的偏好（目标1）。这一阶段的调查结果将用于初步调整我们的拟议方案，以解决这些障碍并确保可接受性。在目标2中，我们将在有风险的青少年的焦点小组中展示这种适应性干预，以获得有关如何适应干预内容，结构和布局以满足青少年需求的信息。在第三阶段，我们将测试招募高危青少年参与适应性干预的可行性，以及适应性干预对抑郁症和危险酒精使用的初步影响。我们将从贫困社区招募100名高危青少年，我们将随机将他们分为接受干预组和对照组。我们将在研究入组后三个月评估干预对抑郁症和酒精使用的影响。一旦三个月的评估完成，对照组的参与者将接受辅导干预。这一阶段的调查结果将用于初步评估干预措施的可行性和效果（目标3 - 4）。如果结果是有希望的，研究结果也将被用来通知一个大型试验的设计，以评估这种干预措施的有效性和成本效益。

项目成果

Brief problem-solving therapy for antenatal depressive symptoms in primary care in rural Ethiopia: protocol for a randomised, controlled feasibility trial.

• DOI: 10.1186/s40814-021-00773-8
• 发表时间: 2021-01-30
• 期刊: Pilot and feasibility studies
• 影响因子: 1.7
• 作者: Bitew T;Keynejad R;Myers B;Honikman S;Medhin G;Girma F;Howard L;Sorsdahl K;Hanlon C
• 通讯作者: Hanlon C

Problem solving therapy (PST) tailored for intimate partner violence (IPV) versus standard PST and enhanced usual care for pregnant women experiencing IPV in rural Ethiopia: protocol for a randomised controlled feasibility trial.

针对亲密伴侣暴力 (IPV) 量身定制的问题解决疗法 (PST) 与标准 PST 相比，并加强对埃塞俄比亚农村经历 IPV 的孕妇的常规护理：随机对照可行性试验方案。

• DOI: 10.1186/s13063-020-04331-0
• 发表时间: 2020
• 期刊: Trials
• 影响因子: 2.5
• 作者: Keynejad RC