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Evaluating the Impact of Emergency Maternity Housing

2022年6月17日 更新者:William Evans、University of Notre Dame

Evaluating the Impact of Emergency Maternity Housing on Mother and Child Well-being, Housing, and Employment

Moms will call and agencies will determine if she is eligible based on basic criteria. If she is eligible, the agency will send her an intake application link to complete, which includes a consent form. After completing the survey, if she is still eligible, she will be placed on a waitlist for services. When a bed becomes available in an individual agency, the agency will call two moms at the top of the waitlist, conduct in-person interviews to confirm eligibility and good fit. They will use a computer to randomly assign one to treatment and one to control. Agency will let moms know of their status and will allow the treatment mom to move in. Moms in treatment and control will be surveyed approximately one year post the mother's reported due date of the child.

研究概览

地位

招聘中

详细说明

The process begins when an expectant month calls a home seeking housing. The maternity home caseworker will ask basic screening questions to determine eligibility. Those found ineligible are referred elsewhere. If the mom is eligible, the caseworker will send her a link to an online application asking a variety of questions surrounding her current housing and employment, health and mental health, other children, criminal justice involvement, etc. The application will include a brief consent form asking for permission to use her information. She will have the option of consenting or not. When she submits her response, the caseworker will be able to review her answers. If there are any answers that would make the mom ineligible at this point, the caseworker will call her and refer her to other local services. If she is still a good fit, the caseworker will call her and let her know that she is eligible but that they don't have any open beds, and that she will be put on a waitlist for the next available bed.

When a bed becomes available, a caseworker will call the top two moms on the waitlist and schedule a time for an in-person interview. They will conduct both interviews to confirm eligibility. After the interview, caseworkers might convene at the home to discuss whether the moms are good fits for group living (for example, the mothers are sometimes unwilling to abide by house rules and they might indicate hesitancy during an interview). If one is not a good fit, the caseworker will let her know she is ineligible and bring in the next mom on the list for an interview. Once two moms are found eligible, the caseworkers will put their names into a separate survey form, which on the backend will randomly assign one to treatment and one to control. The caseworker will call each mom back and let her know if they are going to be able to help her based on her randomization status. Control moms will be referred to other local services. Treatment moms will schedule a time to move in. Both consented and unconsented moms will be randomized the same - having the same odds of receiving services.

Note that three of the five homes will utilize the procedure above. The fourth and fifth homes will complete the same process up to the waitlist stage. Once a bed is available, the caseworker will call the top two moms on the waitlist to confirm they are still interested, then they will randomize them and let them know their status. Only the treatment mom will be brought in for an interview since this home is confident they will be able to determine eligibility based off of the phone and survey application screen and only need the interview to determine services for moms who will actually move into the home.

All moms will complete a follow up survey about one year after the estimated birth of the child (as reported as the due date at baseline).

研究类型

介入性

注册 (预期的)

1048

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:William Evans, PhD
  • 电话号码:5746317039
  • 邮箱:wevans1@nd.edu

研究联系人备份

  • 姓名:Vivian Crumlish, MEd
  • 电话号码:5746311669
  • 邮箱:vcrumlis@nd.edu

学习地点

    • Indiana
      • Notre Dame、Indiana、美国、46556
        • 招聘中
        • University of Notre Dame
        • 接触:
          • William Evans, PhD
          • 电话号码:574-631-7039
          • 邮箱:wevans1@nd.edu
        • 接触:
          • Vivian Crumlish, MEd
          • 电话号码:574-631-1669
          • 邮箱:vcrumlis@nd.edu

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

女性

描述

Inclusion Criteria:

  • Each home has their own eligibility criteria. The main three criteria common across homes are that a woman must be at least 18 years old, experiencing housing instability, and pregnant. No home has an income standard because, by definition, applicants are in a precarious housing situation so most women are low-income. Each home does have slightly different eligibility criteria. For example, some homes allow other children to come with her into the home, while other homes do not. Some homes require a background check and might allow a woman to enter the home anyway depending on the prior offense.

Exclusion Criteria:

  • Women who are not pregnant, men, pregnant women under 18, some homes exclude mothers who have other children currently in their care

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:支持治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
无干预:控制
转介社区提供的其他服务
实验性的:Maternity Home Bed
Receives a bed in the maternity home, wrap-around services, etc.
Receives a bed in the maternity home, wrap-around services, etc.
其他名称:
  • Emergency Maternity Housing

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Difference in rates of self-reported taking baby to term between treatment and control groups
大体时间:1 year after approximate due date of baby
The research team will use self-reported rates of taking the baby to term between treatment and control groups
1 year after approximate due date of baby
Difference in rates of self-reported retaining custody of baby between treatment and control groups
大体时间:1 year after approximate due date of baby
The research team will use survey data to quantify the impact of receiving a bed in the maternity home on self-reported retaining custody of the baby
1 year after approximate due date of baby
Difference in rates of self-reported loneliness and depression between treatment and control groups
大体时间:1 year after approximate due date of baby
The research team will use survey data to quantify the impact of receiving a bed in the maternity home on self-reported loneliness and depression levels.
1 year after approximate due date of baby
Difference in rates of self-reported life satisfaction between treatment and control groups
大体时间:1 year after approximate due date of baby
The research team will use survey data to quantify the impact of receiving a bed in the maternity home on self-reported life satisfaction
1 year after approximate due date of baby
Difference in rates of self-reported sense of self-efficacy between treatment and control groups
大体时间:1 year after approximate due date of baby
The research team will use survey data to quantify the impact of receiving a bed in the maternity home on self-reported sense of self-efficacy
1 year after approximate due date of baby
Difference in housing stability between treatment and control groups
大体时间:1 year after approximate due date of baby
The research team will use self-reported independent living status and whether the mom has a mortgage or lease in her own name at the time of follow to quantify the impact of receiving a bed in the maternity home on housing stability.
1 year after approximate due date of baby
Difference in rates of continuum of care utilization between treatment and control groups
大体时间:1 year after approximate due date of baby
The research team will use mother's interactions with other local service agencies involved in the locality's continuum of care system to quantify the impact of receiving a bed in the maternity home on continuum of care interactions.
1 year after approximate due date of baby
Difference in employment rates between treatment and control groups
大体时间:1 year after approximate due date of baby
The research team will use survey data to quantify the impact of receiving a bed in the maternity home on self-reported employment.
1 year after approximate due date of baby
Difference in safety-net utilization rates between treatment and control groups
大体时间:1 year after approximate due date of baby
The research team will use survey data to quantify the impact of receiving a bed in the maternity home on self-reported amount of welfare received, for example TANF, WIC, SNAP, etc.
1 year after approximate due date of baby
Difference in education rates between treatment and control groups
大体时间:1 year after approximate due date of baby
The research team will use survey data to quantify the impact of receiving a bed in the maternity home on self-reported education level.
1 year after approximate due date of baby

次要结果测量

结果测量
措施说明
大体时间
Difference in housing stability between treatment and control groups
大体时间:1 year after approximate due date of baby
The research team will explore using information from Infutor Data Solutions to also capture address changes and will compare these findings with the self-reported information about housing. Infutor data will only be an exploratory outcome.
1 year after approximate due date of baby

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Adrienne Sabety, PhD、University of Notre Dame
  • 首席研究员:William Evans, PhD、University of Notre Dame
  • 首席研究员:Jessica Brown, PhD、University of South Carolina

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2022年5月30日

初级完成 (预期的)

2025年12月1日

研究完成 (预期的)

2025年12月1日

研究注册日期

首次提交

2022年5月29日

首先提交符合 QC 标准的

2022年6月17日

首次发布 (实际的)

2022年6月23日

研究记录更新

最后更新发布 (实际的)

2022年6月23日

上次提交的符合 QC 标准的更新

2022年6月17日

最后验证

2022年5月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • 22-04-7182

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

We plan to create a de-identified dataset of participant data, which we will make available for other researchers. This dataset will contain the data necessary to replicate the analysis detailed in publications resulting from the study. We will only share data in a manner consistent with data sharing agreements which we establish with data providers. These data sharing agreements are still in process, so while we plan to share de-identified data at this time, we will only do so if our data sharing agreements allow it.

IPD 共享时间框架

We will make data available when we release a publication resulting from the study. There will not be an end date for when data will be available.

IPD 共享访问标准

We will make our dataset available to the general public by posting it on the website for the Inter-University Consortium for Political and Social Research (ICPSR).

IPD 共享支持信息类型

  • 研究方案
  • 树液
  • 国际碳纤维联合会
  • 分析代码
  • 企业社会责任

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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