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H3: Healthy Minds, Healthy Children, Healthy Chicago Project Evaluation (H3)

2019年9月26日 更新者:Bonnie Zima, MD MPH、University of California, Los Angeles

The goal of this project is to develop and pilot test a community-based integrated care model to improve the prevention, early detection and treatment of child mental health problems that is replicable, effective, and sustainable. Project procedures include child mental health screening, on-site brief mental health interventions, referral to specialty mental health, use of co-located child psychiatrist, detection of need for primary care in specialty mental health program. Subjects will be enrolled for 1 year, with interviews at baseline and 3, 6 and 12 months.

Dr. Bonnie Zima at UCLA has been contracted by the project funder to design and implement the evaluation of the project, which includes developing data collection procedures, training staff on implementation of data collection workflow, coordinating with sites to ensure evaluation design and IRB protocols are followed, and coordinating with both study sites to verify data reliability.

Some potential anticipated risks include being uncomfortable answering questions associated with the measures used in the study, and although unlikely, someone may access participant information that is confidential. Some benefits include helping to find ways to improve how to deliver mental health care for children served in publicly-funded primary care and mental health clinics.

調査の概要

詳細な説明

UCLA is in charge of the evaluation of the H3 project, including evaluation design and overseeing data collection by project sites. UCLA will receive data collected by each site and perform the analysis of the data for the sites to be shared with the Illinois Children's Healthcare Foundation and clinic sites. This study will evaluate an existing intervention, meaning that participation in the evaluation is not required in order to receive H3 services.

The information below is included in the evaluation design document attached in 10.1, 1.0:

The overarching goal of the Healthy Minds, Healthy Children, Healthy Chicago Initiative (H3) is to develop a community-based integrated care model to improve the prevention, early detection and treatment of child mental health problems that is replicable, effective, and sustainable.

The final study design is a longitudinal cohort study of 400 children ages 0-17 years and their families served at the two intervention clinic sites (n=200/site) The study time points are baseline, 3-, 6-, and 12-months.

The data sources are parent and youth report, and clinic administrative data when feasible for the programs to transfer these data following IRB-approved procedures. The unit of analysis is the child. The main proximal (or short term) clinical outcomes are related to the H3 intervention care processes (e.g., brief mental health interventions, referral to specialty mental health care, co-located child psychiatrist). The time period will likely vary by child depending on clinical need, but it is anticipated that most of these care processes will be provided during the early phase when the child and parent is introduced to the new care model. The main distal outcomes (or more long-term) are clinical improvement (e.g., child symptom reduction, improved functioning) and some correspond to the care process delivered (e.g., if parent receives parent training, improvement parenting skills are assessed). The time points for tracking clinical improvement are 3, 6 and 12 months after the baseline interview that is done when the parent and child are enrolled in the evaluation. The independent variables (or factors that may influence care processes and clinical outcomes) are child sociodemographic characteristics (e.g. age, sex, race/ethnicity), psychosocial complexity, and primary caregiver characteristics that the clinic team or Community Advisory Board deemed relevant (e.g., parenting stress, probable depression). Embedded within the description of a child's psychosocial complexity are indicators of social determinants (e.g. exposure to trauma) that may adversely impact a child's development and well-being.

Findings from this evaluation will provide data on the acceptability and feasibility of the H3 care models, as well as early indicators of whether these care models are promising.

研究の種類

介入

入学 (実際)

277

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。

研究場所

    • Illinois
      • Chicago、Illinois、アメリカ、60621
        • Miles Square Health Center, Englewood
      • Chicago、Illinois、アメリカ、60622
        • Erie Family Health Center, West Town

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

16年歳未満 (子)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

Inclusion Criteria:

  • between the ages of 0.0-16.99 years
  • speaks Spanish or English
  • screens positive for a developmental delay or mental health problem
  • referral to the H3 care program by a pediatrician based on clinical judgment
  • no prior history of receiving any H3 services in the past year

Exclusion Criteria (based on the child's characteristics):

  • 17 years old (to avoid reconsent at 12 month follow-up)
  • has previously had H3 services in the past year
  • can not speak English or Spanish

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:ヘルスサービス研究
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • 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
実験的:H3 Parent/Child Dyads
A child is eligible for the H3 partnered evaluation if he or she is: 1) between the ages of 0.0-16.99 years; 2) speaks Spanish or English; 3) screens positive for a developmental delay or mental health problem. For children in the intervention groups, the additional eligibility criteria are: 1) referral to the H3 care program by a pediatrician based on clinical judgment; and 2) no prior history of receiving any H3 services in the past year.
A community-based integrated care model to improve the prevention, early detection and treatment of child mental health problems

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
H3 intervention care processes
時間枠:12 months
tracking administration (yes/no) of "brief mental health interventions", "referral to specialty mental health care", "use of co-located child psychiatrist", "detected need for primary care"
12 months

二次結果の測定

結果測定
メジャーの説明
時間枠
Mental health functioning
時間枠:Baseline, 3, 6 and 12 months
PHQ9
Baseline, 3, 6 and 12 months
Child development
時間枠:12 monthsBaseline, 3, 6 and 12 months
Pediatric Symptom Checklist
12 monthsBaseline, 3, 6 and 12 months
Child functioning
時間枠:Baseline, 3, 6 and 12 months
Columbia Impairment Scale
Baseline, 3, 6 and 12 months
Response to trauma and resilience
時間枠:Baseline, 3, 6 and 12 months
Traumatic Events Screening Inventory
Baseline, 3, 6 and 12 months
Care process delivered
時間枠:Baseline, 3, 6 and 12 months
Questionnaire administered at baseline, 3, 6, and 12 months asking parent and child about any care processes that he/she received.
Baseline, 3, 6 and 12 months

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。

捜査官

  • 主任研究者:Bonnie Zima, MD, MPH、University of California, Los Angeles

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

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)

2016年3月1日

一次修了 (実際)

2018年8月1日

研究の完了 (実際)

2019年3月31日

試験登録日

最初に提出

2016年1月25日

QC基準を満たした最初の提出物

2016年3月2日

最初の投稿 (見積もり)

2016年3月4日

学習記録の更新

投稿された最後の更新 (実際)

2019年9月30日

QC基準を満たした最後の更新が送信されました

2019年9月26日

最終確認日

2019年9月1日

詳しくは

本研究に関する用語

キーワード

追加の関連 MeSH 用語

その他の研究ID番号

  • IRB#15-000757

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