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Evaluating the Impact of Emergency Maternity Housing

17 de junho de 2022 atualizado por: 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.

Visão geral do estudo

Status

Recrutamento

Intervenção / Tratamento

Descrição detalhada

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).

Tipo de estudo

Intervencional

Inscrição (Antecipado)

1048

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

  • Nome: William Evans, PhD
  • Número de telefone: 5746317039
  • E-mail: wevans1@nd.edu

Estude backup de contato

  • Nome: Vivian Crumlish, MEd
  • Número de telefone: 5746311669
  • E-mail: vcrumlis@nd.edu

Locais de estudo

    • Indiana
      • Notre Dame, Indiana, Estados Unidos, 46556
        • Recrutamento
        • University of Notre Dame
        • Contato:
          • William Evans, PhD
          • Número de telefone: 574-631-7039
          • E-mail: wevans1@nd.edu
        • Contato:
          • Vivian Crumlish, MEd
          • Número de telefone: 574-631-1669
          • E-mail: vcrumlis@nd.edu

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

18 anos e mais velhos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Sim

Gêneros Elegíveis para o Estudo

Fêmea

Descrição

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

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Cuidados de suporte
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Sem intervenção: Ao controle
Encaminhado para outros serviços disponíveis na comunidade
Experimental: 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.
Outros nomes:
  • Emergency Maternity Housing

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Difference in rates of self-reported taking baby to term between treatment and control groups
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Difference in housing stability between treatment and control groups
Prazo: 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

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Investigador principal: Adrienne Sabety, PhD, University of Notre Dame
  • Investigador principal: William Evans, PhD, University of Notre Dame
  • Investigador principal: Jessica Brown, PhD, University of South Carolina

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

30 de maio de 2022

Conclusão Primária (Antecipado)

1 de dezembro de 2025

Conclusão do estudo (Antecipado)

1 de dezembro de 2025

Datas de inscrição no estudo

Enviado pela primeira vez

29 de maio de 2022

Enviado pela primeira vez que atendeu aos critérios de CQ

17 de junho de 2022

Primeira postagem (Real)

23 de junho de 2022

Atualizações de registro de estudo

Última Atualização Postada (Real)

23 de junho de 2022

Última atualização enviada que atendeu aos critérios de controle de qualidade

17 de junho de 2022

Última verificação

1 de maio de 2022

Mais Informações

Termos relacionados a este estudo

Termos MeSH relevantes adicionais

Outros números de identificação do estudo

  • 22-04-7182

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

SIM

Descrição do plano IPD

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.

Prazo de Compartilhamento de IPD

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.

Critérios de acesso de compartilhamento IPD

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).

Tipo de informação de suporte de compartilhamento de IPD

  • PROTOCOLO DE ESTUDO
  • SEIVA
  • CIF
  • ANALYTIC_CODE
  • CSR

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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