Transforming Care and Payment Priorities for Vulnerable Families
- Conditions
- Social Stress
- Interventions
- Other: Screening survey and accompanying handout for resources
- Registration Number
- NCT03416712
- Lead Sponsor
- Baylor College of Medicine
- Brief Summary
This will be a randomized control trial of 800 children admitted to the Pediatric Hospital Medicine service at Texas Children's Hospital. Each eligible participant will give informed consent prior to enrollment. Study participants will be randomized into an intervention (400 participants) or control group (400 participants). The intervention group will receive a survey (WE CARE HOUSTON) that has been designed to assess family need for community resources that address the SDH (such as food insecurity, housing insecurity, etc.). The intervention group will receive referrals to community resources based on their responses to the WE CARE HOUSTON survey.
- Detailed Description
This will be a randomized control trial of 800 children admitted to the Pediatric Hospital Medicine service at Texas Children's Hospital. Each eligible participant will give informed consent prior to enrollment.
Study participants will be randomized into an intervention (400 participants) or control group (400 participants). The intervention group will receive a survey (WE CARE HOUSTON) that has been designed to assess family need for community resources that address the SDH (such as food insecurity, housing insecurity, etc.). The intervention group will receive referrals to community resources based on their responses to the WE CARE HOUSTON survey. The intervention group will receive a phone call within 3 months of discharge to ask if they have had trouble following up with resources.
Both the intervention and the control groups will be followed for 6 months. Study investigators will obtain outcome data through structured telephone interviews at 6 months and also through medical record review.
This research has been designed to test our hypotheses:
1. The use of the WE CARE HOUSTON screening tool and subsequent referral to community resources will result in increased family participation in community resources that address the SDH; i.e. we believe that the intervention group will enroll in more community resources than the control group over the 6 month study period.
2. The use of the WE CARE HOUSTON screening tool and subsequent referral to community resources will result in improved health outcomes, i.e. children in the intervention group will have fewer emergency department visits, fewer readmissions, improved BMI and improved parent perception of child's health during the study period.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 430
- Children admitted to pediatric hospital medicine service
- Children in child protective service custody
- Children residing outside of the greater Houston area
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Intervention Screening survey and accompanying handout for resources The intervention group will complete a short survey called the WE CARE HOUSTON survey. The WE CARE HOUSTON survey has been designed to quickly assess patient need for local services that address the social determinants of health. The WE CARE HOUSTON survey will be administered on paper or verbally if family is not able to read. Based on the parent's responses to the screening survey, the study investigators will use an algorithm to direct families to appropriate services and community resources. Families who screen positive for social needs will receive a handout on resources. For the families that screen positive for depression/ mental health needs, domestic violence, or alcohol and drug abuse, the study investigators will notify the medical/clinical team and recommend an inpatient social work prior to discharge. Intervention participants will be called 1 week-2 months after enrollment to follow up on resources and will be called for a 6 month follow up structured telephone survey.
- Primary Outcome Measures
Name Time Method Enrollment (yes/no) in social determinant of health resources based on answer to questionnaire 6 months after study enrollment We will assess whether study participants followed up with the resources provided and were able to enroll in needed resources with follow up phone call.
- Secondary Outcome Measures
Name Time Method Child's immunization status 6 months after study enrollment Self report of compliance with vaccinations by parents on follow up survey
Decreased emergency department revisits and hospital readmissions 6 months after study enrollment We will assess whether children in the intervention group will have fewer quantity of all cause emergency department visits, fewer quantity of hospital readmissions on chart review.
Improved parental perception of child's health study enrollment to 6 months after enrollment We will compare caregiver's baseline and 6 month self-rating of their child's health in categories of "excellent", "good", "fair" or "poor".
Child's growth 6 months after study enrollment Weight and height will be combined to report BMI in kg/m\^2. If height is unavailable, weight will be used and reported in kilograms.
Trial Locations
- Locations (1)
Texas Children's Hospital
🇺🇸Houston, Texas, United States