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The e-SINCERE Study

Enhanced Digital Access to Bridge Social Needs and Reduce Health Disparities: The e-SINCERE Study

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07174466
Acronym
e-SINCERE
Enrollment
600
Registered
2025-09-16
Start date
2025-08-08
Completion date
2029-08-31
Last updated
2025-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Digital Health Literacy, Health Services Utilization, Social Determinants of Health (SDOH)

Brief summary

The e-SINCERE study will evaluate whether providing stable cell phones and digital navigation assistance helps patients overcome ICT barriers and connect more successfully with community services. The study will begin with patients in the UHealth ED, with additional sites added in the future, and will involve working with community service providers and policy leaders to refine and implement the intervention. Findings from this study may guide the development of future programs and policies to improve access to services for patients facing economic and technological barriers.

Interventions

OTHERStandard Referral to 211

Participants receive a standard referral to United Way 211 for assistance with social needs. 211 specialists contact referred patients, provide available service referrals, and follow up in an ad-hoc manner as per standard 211 protocols.

BEHAVIORALe-SINCERE (Phone Support)

Participants receive a study-provided cellphone to ensure stable phone access. Using this device, participants are connected to United Way 211 specialists, who provide referral services for identified social needs. This intervention focuses on overcoming communication barriers that might otherwise prevent successful service connection.

BEHAVIORALe-SINCERE (Digital Navigation)

Participants receive a study-provided TracFone and direct support from a trained Digital Navigator. The Digital Navigator assists participants with accessing United Way 211 services, troubleshooting barriers to phone or internet use, and reinforcing follow-through on referrals. This arm is designed to provide enhanced, structured navigation support to address digital access barriers and increase successful service connections.

Sponsors

National Institute of Nursing Research (NINR)
CollaboratorNIH
Andrea Wallace
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Masking description

Services to which participants are referred will not be aware of the participant's inclusion in the research study or their study arm.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Community Advisory Board Members Health system, governmental, and community service stakeholders Able to understand English Adult (\> 18 years) \- General screening population: Any patient who completes the SINCERE screener. Able to understand or read English or Spanish. \- Survey study inclusion criteria: Any patient who completes the SINCERE screener who has connected with 211 for service outreach Able to understand or read English or Spanish. Adult (\> 18 years)

Exclusion criteria

* Those unable to communicate verbally in English or Spanish * Those living in nursing facilities, or those who are not otherwise responsible for self-care

Design outcomes

Primary

MeasureTime frameDescription
Successful connection to community social services (any service)6 months after randomizationProportion of participants who have at least one documented successful connection to a community social service (e.g., housing assistance, utilities, food support, transportation) within 6 months. Successful connection is defined as a recorded positive outcome in 211 or ServicePoint (client reached and service initiated) or participant self-report confirmed by case notes.

Secondary

MeasureTime frameDescription
Health-related quality of life (PROMIS Global Health)Baseline, 2 weeks, 3 months, and 6 months after randomizationChange in PROMIS Global Health T-score from baseline to 6 months. Higher scores indicate better overall physical and mental health. Analysis will compare mean change between arms.
Emergency department utilization (all-cause ED visits)6 months after randomizationNumber of all-cause ED visits per participant during the 6-month follow-up period, obtained from the institution's EDW and participant self-report for non-UHealth visits. Analysis will compare mean visits and proportion with any ED revisit between arms.
Digital access stability (phone connectivity)6 months after randomizationProportion of participants in the phone/navigation arms with continuous phone connectivity (TracFone active and reachable) for at least 5 of 6 months. Connectivity assessed via phone service logs and navigator contact attempts.

Countries

United States

Contacts

Primary ContactErnest Grigorian, MS
Ernest.Grigorian@utah.edu801-585-7194

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 26, 2026