Zandbergen M M E, Jansen E E L, Jabbarian L J, de Koning H J, de Kok I M C M
Department of Public Health, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.
MiSi NeuroPsy, Rotterdam, the Netherlands.
BMC Psychol. 2024 Dec 18;12(1):742. doi: 10.1186/s40359-024-02230-6.
Mobile-based screening interventions to detect and treat Major Depressive Disorder (MDD) at an early stage might be a promising approach for reducing its societal burden. In the present study, we will evaluate the feasibility and effectiveness of screening for MDD using a mobile-based screening protocol.
This study will be a three-arm, parallel randomized control trial (RCT) performed in a multi-ethnic population within the municipality of Rotterdam (the Netherlands). The trial includes two intervention groups that will be screened 4-weekly for MDD for 12 months using the Patient Health Questionnaire (PHQ-9) and a control group who does not receive mobile-based screening for MDD. Participants in the one-test intervention arm will be referred for further diagnosis and treatment, if necessary, after a single positive test score for moderate-severe major depression symptoms (PHQ-9 > 10). Participants in the multiple-test intervention arm will only be referred after three consecutive positive test scores. 1786 eligible participants will be included in the RCT, with 446 and 447 in the one-test and multiple-test referral arms, respectively, and 893 in the control arm. Primary outcome is participants' QoL after 12 months (EQ-5D-5L). Secondary outcomes include participants' QoL after 24 months (EQ-5D-5L), evaluating the occurrence and severity of MDD symptoms (PHQ-9), intervention engagement, and identifying public mental health differences based on sociodemographic characteristics, including age, gender, ethnicity, financial situation, educational background, and living area. Long-term results of the RCT will be incorporated into a microsimulation model to determine the long-term benefits, harms, and costs of MDD screening.
The information gained from examining the feasibility and (cost-) effectiveness of mobile-based screening for MDD could be of guidance for mental health policy implementations and support the introduction of mobile-based screening for MDD in the Netherlands and/or other nations.
ClinicalTrials.gov: NL84280.078.23, NCT05989412 , August 8, 2024.
基于移动设备的筛查干预措施,用于早期发现和治疗重度抑郁症(MDD),可能是减轻其社会负担的一种有前景的方法。在本研究中,我们将评估使用基于移动设备的筛查方案筛查MDD的可行性和有效性。
本研究将在鹿特丹市(荷兰)的多民族人群中进行一项三臂平行随机对照试验(RCT)。该试验包括两个干预组,将使用患者健康问卷(PHQ-9)每4周对MDD进行12个月的筛查,以及一个未接受基于移动设备的MDD筛查的对照组。单测干预组的参与者在单次中度至重度重度抑郁症状阳性测试分数(PHQ-9>10)后,如有必要,将被转介进行进一步诊断和治疗。多测干预组的参与者只有在连续三次阳性测试分数后才会被转介。1786名符合条件的参与者将被纳入RCT,单测和多测转介组分别有446名和447名,对照组有893名。主要结局是12个月后参与者的生活质量(EQ-5D-5L)。次要结局包括24个月后参与者的生活质量(EQ-5D-5L)、评估MDD症状的发生和严重程度(PHQ-9)、干预参与度,以及根据社会人口学特征(包括年龄、性别、种族、财务状况、教育背景和居住地区)确定公共心理健康差异。RCT的长期结果将纳入微观模拟模型,以确定MDD筛查的长期益处、危害和成本。
从检查基于移动设备的MDD筛查的可行性和(成本)效益中获得的信息,可为心理健康政策的实施提供指导,并支持在荷兰和/或其他国家引入基于移动设备的MDD筛查。
ClinicalTrials.gov:NL84280.078.23,NCT05989412,2024年8月8日。