RECRUITING

MOLAR: Mapping Oral Health and Local Area Resources

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

MOLAR: Mapping Oral Health and Local Area Resources

Quick Facts

Study Start:2023-08-25
Study Completion:2028-02-22
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05688982

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:1 Year
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * To be eligible to participate in this study, an individual must meet all of the following criteria:
  2. * No evidence of lack of capacity to provide verbal informed consent (as documented in the chart).
  3. * Willing to comply with all study procedures and be available by phone for the duration of the study (as reported by the patient)
  4. * Unmet oral health needs as ascertained by the Hope Home (adult) or Gazzaz (pediatric) questions
  5. * 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.
  6. * Ability to communicate in English or Spanish (as reported by the patient)
  7. * Emergency severity index (ESI) 2-5 (as documented in the electronic medical record)
  8. * Residence within catchment area of 3-hospital region (defined by MGB home hospital catchment area) at initial enrollment (as reported by the patient)
  9. * Working phone number
  1. * Patients on involuntary holds (per electronic medical record review)
  2. * Presenting from carceral facilities (per electronic medical record review)
  3. * Presenting for acute mental health care under evaluation for Section 12 (per electronic medical record review)
  4. * Patients presenting for assistance with intimate partner violence (IPV) or care following sexual assault

Contacts and Locations

Study Contact

Margaret Samuels-Kalow
CONTACT
617-726-8340
msamuels-kalow@partners.org

Study Locations (Sites)

Massachusetts General Hospital
Boston, Massachusetts, 02114
United States

Collaborators and Investigators

Sponsor: Massachusetts General Hospital

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-08-25
Study Completion Date2028-02-22

Study Record Updates

Study Start Date2023-08-25
Study Completion Date2028-02-22

Terms related to this study

Additional Relevant MeSH Terms

  • Dental Diseases