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一项基于应用程序的世界卫生组织抑郁症检测心理健康指南:一项整群随机临床试验。

An App-Based WHO Mental Health Guide for Depression Detection: A Cluster Randomized Clinical Trial.

作者信息

Kohrt Brandon A, Ojagbemi Akin, Luitel Nagendra P, Bakolis Ioannis, Bello Toyin, McCrone Paul, Taylor Salisbury Tatiana, Jordans Mark J D, Votruba Nicole, Carswell Kenneth, Green Eric, Gkaintatzi Evdoxia, Lamichhane Bishnu, Elugbadebo Olufisayo, Kola Lola, Lempp Heidi, Chowdhary Neerja, Dua Tarun, Gureje Oye, Thornicroft Graham

机构信息

Center for Global Mental Health Equity, Department of Psychiatry and Behavioral Health, The George Washington University, Washington, DC.

World Health Organization Collaborating Centre for Research and Training in Mental Health, Neuroscience, and Substance Abuse, Department of Psychiatry, College of Medicine, University of Ibadan, Ibadan, Nigeria.

出版信息

JAMA Netw Open. 2025 May 1;8(5):e2512064. doi: 10.1001/jamanetworkopen.2025.12064.

Abstract

IMPORTANCE

Depression detection in primary care remains limited in low- and middle-income countries despite increasing use of the World Health Organization Mental Health Gap Action Programme-Intervention Guide (mhGAP-IG).

OBJECTIVE

To test an app version of the mhGAP-IG (e-mhGAP-IG) in Nepal and Nigeria to improve depression detection.

DESIGN, SETTING, AND PARTICIPANTS: In this feasibility cluster randomized clinical trial conducted from February 14, 2021, to March 25, 2022, primary care facilities (unit of clustering) in Nepal and Nigeria were randomized to the standard mhGAP-IG training arm (control) or to training using the e-mhGAP-IG app (intervention). Primary care workers (PCWs) received training based on the arm assignment of their health care facility. Statistical analysis was conducted from July 20, 2022, through September 27, 2024.

INTERVENTION

Training using standard mhGAP-IG vs training using the e-mhGAP-IG.

MAIN OUTCOMES AND MEASURES

Analysis was performed on an intention-to-treat basis. The main outcome was accuracy of depression detection rates by PCWs, evaluated prior to mhGAP training and 5 to 8 months after training, measured as the percentage of patients who received a depression diagnosis by their PCWs compared with the number of patients who scored 10 or more on the locally validated 9-item Patient Health Questionnaire. Costs per patient detected were calculated.

RESULTS

In Nepal, 25 facilities (67 PCWs; mean [SD] age, 35.3 [9.2] years; 52 men [78%]) were randomized: 13 facilities to standard mhGAP-IG training (36 PCWs) and 12 facilities to e-mhGAP-IG (31 PCWs). In Nigeria, 10 facilities (47 PCWs; mean [SD] age, 46.9 [7.5] years; 44 women [94%]) were randomized: 5 facilities to standard mhGAP-IG (25 PCWs) and 5 facilities to e-mhGAP-IG (22 PCWs). In Nepal, depression detection by PCWs in the standard mhGAP-IG arm increased from 0 of 43 patients before training to 15 of 92 patients after training (adjusted mean change [AMC], 16% [95% CI, 5%-28%]), and depression detection in the e-mhGAP-IG arm increased from 0 of 49 before training to 22 of 91 after training (AMC, 24% [95% CI, 12%-36%]). In Nigeria, depression detection in the standard mhGAP-IG arm increased from 5 of 36 patients before training to 25 of 75 patients after training (AMC, 19% [95% CI, 2%-37%]), and depression detection in the e-mhGAP-IG arm increased from 6 of 35 patients before training to 67 of 76 patients after training (AMC, 71% [95% CI, 57%-85%]). In facilities in the e-mhGAP-IG arm, the app was used for 59 of 616 assessments (10% of patients) in Nepal and 883 of 1077 assessments (82% of patients) in Nigeria. Cost per patient with depression detected using the e-mhGAP-IG was Nepali Rupiya (NPR) 1980 (US $14.79) in Nepal and naira (₦) 1462 (US $0.91) in Nigeria.

CONCLUSIONS AND RELEVANCE

This feasibility cluster randomized clinical trial demonstrated that the use, cost, and potential clinical benefit of the e-mhGAP-IG varied by setting, highlighting the importance of multisite feasibility studies when evaluating digital innovations intended for health care systems worldwide.

TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT04522453.

摘要

重要性

尽管世界卫生组织的《精神卫生差距行动规划干预指南》(mhGAP-IG)的使用日益增加,但低收入和中等收入国家初级保健中的抑郁症检测仍然有限。

目的

在尼泊尔和尼日利亚测试mhGAP-IG的应用程序版本(电子mhGAP-IG),以改善抑郁症检测。

设计、设置和参与者:在这项于2021年2月14日至2022年3月25日进行的可行性整群随机临床试验中,尼泊尔和尼日利亚的初级保健机构(整群单位)被随机分配到标准mhGAP-IG培训组(对照组)或使用电子mhGAP-IG应用程序进行培训(干预组)。初级保健工作者(PCW)根据其医疗机构的分组分配接受培训。统计分析于2022年7月20日至2024年9月27日进行。

干预措施

使用标准mhGAP-IG进行培训与使用电子mhGAP-IG进行培训。

主要结局和测量指标

基于意向性分析进行分析。主要结局是PCW检测抑郁症的准确率,在mhGAP培训前和培训后5至8个月进行评估,以PCW诊断为抑郁症的患者数量占在当地验证的9项患者健康问卷中得分10分或更高的患者数量的百分比来衡量。计算每位检测出抑郁症的患者的成本。

结果

在尼泊尔,25个机构(67名PCW;平均[标准差]年龄,35.3[9.2]岁;52名男性[78%])被随机分组:13个机构接受标准mhGAP-IG培训(36名PCW),12个机构接受电子mhGAP-IG培训(31名PCW)。在尼日利亚,10个机构(47名PCW;平均[标准差]年龄,46.9[7.5]岁;44名女性[94%])被随机分组:5个机构接受标准mhGAP-IG培训(25名PCW),5个机构接受电子mhGAP-IG培训(22名PCW)。在尼泊尔,标准mhGAP-IG组中PCW检测抑郁症的比例从培训前43名患者中的0例增加到培训后92名患者中的15例(调整后平均变化[AMC],16%[95%CI,5%-28%]),电子mhGAP-IG组中抑郁症检测从培训前49名患者中的0例增加到培训后91名患者中的22例(AMC,24%[95%CI,12%-36%])。在尼日利亚,标准mhGAP-IG组中抑郁症检测从培训前36名患者中的5例增加到培训后75名患者中的25例(AMC,19%[95%CI,2%-37%]),电子mhGAP-IG组中抑郁症检测从培训前35名患者中的6例增加到培训后76名患者中的67例(AMC,71%[95%CI,57%-85%])。在电子mhGAP-IG组的机构中,该应用程序在尼泊尔616次评估中的59次(10%的患者)和尼日利亚1077次评估中的883次(82%的患者)中被使用。在尼泊尔,使用电子mhGAP-IG检测出抑郁症的每位患者的成本为1980尼泊尔卢比(14.79美元),在尼日利亚为1462奈拉(0.91美元)。

结论和相关性

这项可行性整群随机临床试验表明,电子mhGAP-IG的使用、成本和潜在临床益处因环境而异,突出了在评估适用于全球医疗保健系统的数字创新时进行多地点可行性研究的重要性。

试验注册

ClinicalTrials.gov标识符:NCT04522453。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c34/12102703/b573e0aa5fbb/jamanetwopen-e2512064-g001.jpg

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