Housing Prescriptions as Health Care
Housing Prescription
Autre étude
Résumé
Date de début de l'étude : 1 octobre 2016
Date à laquelle le premier participant a commencé l'étude.Background: Housing insecurity is a known risk factor for negative child health and developmental outcomes. The goal of this intervention is to reduce housing insecurity among families with young children as a mechanism for improving child health and improving other predictors on the pathway toward child health, including food security and maternal mental health status. Rationale: Children's HealthWatch data collected from 2010-2014 at Boston Medical Center, where the sample for this project will be recruited, found 32% of families were behind on rent in the past year and 7% of families moved more than twice in the past year. Previous research by Children's HealthWatch links multiple moves with increased risks of fair or poor child health and developmental delay. Families who are behind on rent are also at risk of fair or poor health, developmental delays, and are below average in length/height, a marker for under-nutrition. Given the significant associations between housing insecurity and child health outcomes, this project is tailored to address challenges faced by families who are severely housing insecure and who are classified as high health care utilizers by industry standards (defined as ≥ 3 emergency department visits in one year). This research study design for this pilot is a randomized control trial whereby eligible families are randomly assigned to the intervention group or the control group. Those in the intervention group will be referred to a case manager and receive at least one of the six services offered through the program. Families in the control group will receive the current standard of care, which is a packet of outreach resources with information on housing and housing supports. Purpose: This study will investigate if this intervention is effective in improving housing stability and child health outcomes compared to current standard of care. Study hypotheses: Using data collected at baseline, six months, and 12 months after enrollment, the investigators will examine whether children ages 0-4, their siblings ages 0-11, and caregivers in the intervention group, vs. those in the control group, are more likely to have: * Reduced score on housing insecurity assessment * Reduced emergency department (ED) usage and hospitalizations for caregivers and children * Improved adherence to well-child visits and immunization schedule * Improved caregiver mental health, as defined by reduced depressive symptoms reported * Increased family income and reduced reports of material hardships, including decreased food insecurity, defined by the gold-standard USDA 18-item scale; decreased energy insecurity, using the validated Children's HealthWatch screener; and decreased health care hardships, using the Children's HealthWatch screener. The investigators will also examine ultimate net cost vs. savings per consumer to implement this Housing Prescription as Health Care program. Elements we will consider in economic models include: * Costs of delivery of the intervention * Savings from avoided health care costs * Savings from avoided homelessness * Increased family income as a result of this intervention
Protocole
Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.78 participants à inclure
Nombre total de participants que l'essai clinique vise à recruter.Autre
Éligibilité
Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.Tout sexe
Le sexe biologique des participants éligibles à s'inscrire.Volontaires sains autorisés
Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.Critères
Plan de l'étude
Découvrez tous les traitements administrés dans cette étude, leur description détaillée et ce qu'ils impliquent.Un seul groupe d'intervention est désigné dans cette étude
Cette étude ne comporte pas de groupe placebo.
Groupes de traitement
Groupe I
ExpérimentalObjectifs de l'étude
Objectifs principaux
Objectifs secondaires
Centres d'étude
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