Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07196007

Leveraging Community-clinical Linkages to Address Unmet Social Needs for People With Diabetes

This study is a hybrid type 2 design to evaluate the effectiveness and implementation of a community-clinical linkage intervention in primary clinics to address unmet social needs for patients with diabetes living in rural communities. The study will take place in two rural communities in Kentucky, one in eastern Kentucky and one in western Kentucky.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Kentucky

Lexington, Kentucky, 40506, United States

Location status: Recruiting

Location contact

Mary E Lacy, PhD

CONTACT

[email protected]

8595621126

About this study

This study will convene clinical and community partners to complete a rapid process improvement workshop (RPIW) to co-create scalable strategies to address unmet social needs and to implement the developed strategy in primary care clinics in two rural communities in Kentucky. Results from the RPIW will be used to design an implementation template with specific implementation strategies tailored to each unique community-clinical linkage (CCL). While implementation strategies will be tailored to each CCL, the overarching intervention components for all CCL include: 1) patient navigators; 2) health information technology; and 3) quality improvement support to clinical and community partners. The finalized intervention will then be rolled out across partner clinics using a parallel-group cluster design that facilitates pragmatic randomization. The effect of the intervention on referrals will be assessed by comparing referrals between intervention and control clinics. Secondary effectiveness outcomes include status of social needs (improved or not), patient-reported quality of life, and diabetes control (A1c < 9.0% controlled vs A1c =9% uncontrolled). To evaluate implementation outcomes, we will use a mixed methods approach to examine process factors that affect reach, acceptance, and fidelity of the CCL intervention. This approach allows us to examine which strategies can be replicated and scaled up for implementation in other communities.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Clinic/Staff Inclusion Criteria:

  • staff at the intervention or comparison clinic

Participant Inclusion Criteria:

  • age 18 or older,
  • is a patient at the intervention or comparison clinic
  • diagnosed with diabetes

Clinic/Staff Exclusion Criteria:

  • staff not at the intervention or comparison clinic

Participant Exclusion Criteria:

  • being under the age of 18,
  • not a patient at the intervention or comparison clinic
  • not diagnosed with diabetes

Treatment and study plan

Community-Clinical Intervention

Behavioral

The intervention involves enhancing usual care for screening patients with diabetes for unmet social needs and referring those who screen positive to a Community Health Worker. Patients who screen positive for unmet social needs will work with CHWs to be connected to community organizations.

Primary outcomes

  1. Number of participants screened for social needs

    Time frame: Baseline, month 6 and month 12

    Number of participants screened for social needs intervention compared to control

  2. Number of referrals to community based organization by primary care clinic

    Time frame: Baseline, month 6 and month 12

    Number of referrals to community based organization in intervention compared to control

Secondary outcomes

  1. Change in Status of social needs

    Time frame: Baseline, month 6 and month 12

    Change in status of social needs, answered by a yes/no question as to accessed or not. Social needs include food insecurity, housing instability, difficulty with utilities, transportation issues, and intimate partner violence. Data will be reported as aggregate across needs.

  2. Change in Patient-Reported Outcomes Measurement Information System (PROMIS) -29

    Time frame: Baseline, month 6 and month 12

    The PROMIS - 29 measures health-related quality of life across seven domains. Scores are standardized on a T-score metric, with a mean of 50 and a standard deviation of 10 in a referent population. A higher score means more of the concept being measured.

  3. Percent of participants with A1c greater than or equal to 9.0%

    Time frame: Baseline, month 6 and month 12

    Change in A1c level; Diabetes control (A1c < 9.0% controlled vs A1c =9% uncontrolled) via Electronic Health Record extract

Study contacts

Contact information is provided by the study sponsor or research team.

Carol R White, MPH

CONTACT

[email protected]

859-562-2684

Mary Lacy Leigh, PhD

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

Mary Lacy

Other

Collaborators

  • Centers for Disease Control and Prevention

Registry information

Official study title

Leveraging Community-clinical Linkages to Address Unmet Social Needs for People With Diabetes Living in Rural Settings

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Sep 29, 2025
Registry last updated
Mar 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.