Perinatal Mortality Outcomes Through Household Infection Pathways (POTH)
Effect of Cement Floors on Perinatal and Neonatal Mortality in Bangladesh: a Randomized Trial in Rural Bangladesh
The goal of this trial is to learn if replacing household soil floors with concrete floors can prevent deaths of infants around the time of birth, including stillbirths and deaths in the first month of life in rural Bangladesh. The primary question the study aims to answer is: Does residing in a home with a concrete vs. soil floor reduce the perinatal and neonatal morality in index children and their younger siblings up to 6 years post-installation of concrete floors?
Researchers will compare participants in households with concrete floors (intervention) vs. soil floors (comparison group) to see if concrete floors reduce the rate of perinatal death and child death up the 6 years post-intervention.
This study will extend an ongoing NIH-funded randomized trial in which households with soil floors where a pregnant woman resided were randomly chosen to receive a concrete floor intervention or to retain their existing soil floor. This study will track pregnancies, births, and deaths among infants born to pregnant mothers in the original study to measure effects of household concrete flooring up to 6 years after the concrete floors were installed.
調査の概要
詳細な説明
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究場所
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-
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Dhaka、バングラデシュ
- International Centre for Diarrhoeal Disease Research, Bangladesh
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主任研究者:
- Md. Mahbubur Rahman, MBBS
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参加基準
適格基準
就学可能な年齢
- 子
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Prior enrollment in the CRADLE trial (NCT05372068), in either arm, and currently residing in the original CRADLE-enrolled household
- Residence in Sirajganj or Tangail districts in Bangladesh
- No major non-compliance (e.g., no removal of concrete floor in intervention arm or installation of concrete floor in control arm)
- No plan to relocate within the study follow-up period
- Incident pregnancy occurring after CRADLE trial enrollment, confirmed after 26 weeks gestation
研究計画
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:防止
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:独身
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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介入なし:不干渉
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実験的:Concrete household floor
Household soil floors will be replaced with concrete floors
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家庭用の土の床はコンクリートの床に置き換えられます
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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 |
|---|---|---|
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Extended perinatal mortality rate
時間枠:Up to 6 years post-intervention delivery in parent study
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Total number of stillbirths (babies born following fetal deaths at 22 weeks or later gestation) and neonatal deaths within the first 28 days after birth divided by the number of total births (live births + stillbirths)
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Up to 6 years post-intervention delivery in parent study
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Stillbirth rate
時間枠:Up to 6 years post-intervention delivery in parent study
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Total number of stillbirths (babies born following fetal deaths at 22 weeks or later gestation) divided by the number of total births (live births + stillbirths)
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Up to 6 years post-intervention delivery in parent study
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Early neonatal mortality rate
時間枠:Up to 6 years post-intervention delivery in parent study
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Total number of deaths occurring in the first 7 days of life divided by the number of live births
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Up to 6 years post-intervention delivery in parent study
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Neonatal mortality rate
時間枠:Up to 6 years post-intervention delivery in parent study
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Total number of deaths occurring in the first 28 days of life divided by the number of live births
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Up to 6 years post-intervention delivery in parent study
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Infant mortality rate
時間枠:Up to 6 years post-intervention delivery in parent study
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Total deaths prior to age 12 months among live births divided by total live births
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Up to 6 years post-intervention delivery in parent study
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Child mortality rate
時間枠:Up to 6 years post-intervention delivery in parent study
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Total deaths at any age among live births divided by total live births
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Up to 6 years post-intervention delivery in parent study
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協力者と研究者
スポンサー
協力者
捜査官
- 主任研究者:Jade Benjamin-Chung, PhD MPH、Stanford University
出版物と役立つリンク
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- 86289
- 03001 (その他の助成金/資金番号:Thrasher Foundation)
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?
IPD プランの説明
IPD 共有時間枠
IPD 共有アクセス基準
IPD 共有サポート情報タイプ
- STUDY_PROTOCOL
- SAP
- ANALYTIC_CODE
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
米国FDA規制機器製品の研究
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