Overview
The goal of this clinical trial is to test the impact of a screening and linkage intervention for adverse social determinants of health (aSDoH) on oral health linkage to care for emergency department patients. Researchers will compare three groups: Patients in Arm A will receive paper handouts with general oral health and aSDoH resources. Patients in Arm B will receive paper handouts with geographically-proximate oral health and aSDoH resources. Patients in Arm C will receive geographically-proximate oral health and aSDoH resources plus active navigational assistance.
Eligibility
Inclusion Criteria:
- To be eligible to participate in this study, an individual must meet all of the
following criteria:
- No evidence of lack of capacity to provide verbal informed consent (as documented in the chart).
- Willing to comply with all study procedures and be available by phone for the duration of the study (as reported by the patient)
- Unmet oral health needs as ascertained by the Hope Home (adult) or Gazzaz (pediatric) questions
- Adult (age ≥18 years old) ED patient or pediatric ED patient (>1 year of age) presenting with parent or legal guardian. Parent will be the primary study participant but if age > 7 years, the child will provide assent for medical record review.
- Ability to communicate in English or Spanish (as reported by the patient)
- Emergency severity index (ESI) 2-5 (as documented in the electronic medical record)
- Residence within catchment area of 3-hospital region (defined by MGB home hospital catchment area) at initial enrollment (as reported by the patient)
- Working phone number
Exclusion Criteria:
- Patients on involuntary holds (per electronic medical record review)
- Presenting from carceral facilities (per electronic medical record review)
- Presenting for acute mental health care under evaluation for Section 12 (per electronic medical record review)
- Patients presenting for assistance with intimate partner violence (IPV) or care following sexual assault