跳至主要内容
临床试验/NCT01298804
NCT01298804已完成不适用

Preventing Maternal Depression In Head Start

Boston Medical Center2 个研究点 分布在 1 个国家目标入组 230 人开始时间: 2011年2月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
230
试验地点
2
主要终点
Problem Solving Skills

研究概览

简要总结

Maternal depression disproportionately affects low-income and minority women, and has profound negative impacts on their children. The investigators are conducting a randomized trial of a systems approach to identify mothers at risk for depression in Head Start - a federally funded early learning program for children of low-income families - and to provide an on-site intervention to prevent or alleviate depressive symptoms; improve functioning; and, where appropriate, proactively link mothers to more definitive mental health services.

详细描述

This study is one component of a series of studies that aims to develop a comprehensive system of maternal depression prevention and management within Head Start. In our March 2014 review of the CT.gov protocol, we synchronized it with our institution's IRB protocol, which had been modified based on how the individual studies within this series relate to one another. Specifically, the original IRB protocol combined two studies into one: a 'main' depression prevention trial (n=230, R01MH091871), and a small adjunct pilot aimed at referring those with symptoms of major depression to further care (n=60). Thus, the original CT.gov protocol included subjects both at risk for depression and with symptoms consistent with major depression. When the latter pilot study subsequently received external funding, we separated the two studies into two IRB protocols, and thus have adjusted our CT.gov protocol to the appropriate sample size of 230, and indicated symptoms of major depression as an exclusion criterion for the prevention trial. Because Major Depressive Episode was inadvertently listed as a primary outcome measure for the prevention trial (and PTSD and Anxiety as secondary outcome measures), we have removed them as such and listed it under 'other' outcomes, thereby aligning the CT.gov protocol with the statistical analysis plan of the original grant application and IRB protocol. Lastly, we corrected administrative errors in the study's projected end date and masking design.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
15 Years 至 64 Years(Child, Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Family enrolled in Head Start, and child expected to attend Head Start activities for at least 6 months of the 12-month follow-up period.
  • •Family without imminent plans to relocate
  • •Mother is comfortable in English or Spanish.
  • •Parent/guardian who has a child that attends Head Start
  • •Child attending Head Start and is between the ages 0-5
  • •Screen positive to 2-question depression screener (PHQ2), or have a past history of depression
  • •Ability to provide informed consent.
  • •Not suicidal

排除标准

  • •High suicidal ideation
  • •Cognitive limitation
  • •Psychosis
  • •No known risks for depression
  • •Symptoms reflecting major depressive episode

研究组 & 干预措施

Problem Solving Education

Experimental

干预措施: Problem Solving Education and Activated Referral to Care (Behavioral)

Control

No Intervention

结局指标

主要结局

Problem Solving Skills

时间窗: 12 months

Social Problem Solving Inventory

Depression Symptoms

时间窗: 12 months

QIDS

Depression Symptoms

时间窗: 2 months

QIDS

Depression Symptoms

时间窗: 4 months

QIDS

Depression Symptoms

时间窗: 6 months

QIDS

Depression Symptoms

时间窗: 8 months

QIDS

Depression Symptoms

时间窗: 10 months

QIDS

Problem Solving Skills

时间窗: 6 months

Social Problem Solving Inventory

次要结局

  • Social functioning(12 months)
  • Parent functioning/stress(12 months)
  • Receipt of Mental Health Services(12 months)
  • Head Start attendance(12 months)
  • Child Behavior(6 months)
  • Social functioning(6 months)
  • Parent functioning/stress(6 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Michael Silverstein

Associate Professor of Pediatrics

Boston Medical Center

研究点 (2)

Loading locations...

相似试验