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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.

調査の概要

状態

募集

詳細な説明

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).

研究の種類

介入

入学 (予想される)

1048

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

  • 名前:William Evans, PhD
  • 電話番号:5746317039
  • メール:wevans1@nd.edu

研究連絡先のバックアップ

  • 名前:Vivian Crumlish, MEd
  • 電話番号:5746311669
  • メール:vcrumlis@nd.edu

研究場所

    • Indiana
      • Notre Dame、Indiana、アメリカ、46556
        • 募集
        • University of Notre Dame
        • コンタクト:
          • William Evans, PhD
          • 電話番号:574-631-7039
          • メール:wevans1@nd.edu
        • コンタクト:
          • Vivian Crumlish, MEd
          • 電話番号:574-631-1669
          • メール:vcrumlis@nd.edu

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

はい

受講資格のある性別

女性

説明

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

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:支持療法
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
介入なし:コントロール
コミュニティで利用可能な他のサービスを参照した
実験的: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.
他の名前:
  • Emergency Maternity Housing

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Difference in rates of self-reported taking baby to term between treatment and control groups
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
Difference in housing stability between treatment and control groups
時間枠: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

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Adrienne Sabety, PhD、University of Notre Dame
  • 主任研究者:William Evans, PhD、University of Notre Dame
  • 主任研究者:Jessica Brown, PhD、University of South Carolina

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2022年5月30日

一次修了 (予想される)

2025年12月1日

研究の完了 (予想される)

2025年12月1日

試験登録日

最初に提出

2022年5月29日

QC基準を満たした最初の提出物

2022年6月17日

最初の投稿 (実際)

2022年6月23日

学習記録の更新

投稿された最後の更新 (実際)

2022年6月23日

QC基準を満たした最後の更新が送信されました

2022年6月17日

最終確認日

2022年5月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

はい

IPD プランの説明

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 共有時間枠

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 共有アクセス基準

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 共有サポート情報タイプ

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • ANALYTIC_CODE
  • CSR

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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