The Impact of Social Worker Referrals on Diabetes and Loneliness

University of Toronto

Status: Active, not recruiting

Conditions: Diabete Mellitus; Loneliness

Treatments: Behavioral: Social worker referral to address loneliness; Other: Continue Primary care

Study type: Interventional

Funder types: Other

Identifiers

NCT07486050

6941

Details and patient eligibility

About

The goal of this clinical trial is to learn if referral to a social worker (social prescribing) can help reduce loneliness and improve blood sugar control (A1C) in older adults with diabetes. It will also help us understand how this approach can support overall well-being in seniors.

The main questions it aims to answer are:

• Does referral to a social worker reduce feelings of loneliness in older adults with diabetes?
• Does this support improve blood sugar control (A1C)?

Researchers will compare social worker referral to usual diabetes care to see if this approach improves both social well-being and diabetes outcomes.

Participants will:

• Be assigned (like flipping a coin) to either meet with a social worker or continue their usual care
• Complete a short 3-question loneliness survey at the start and again after 6 months
• Have their A1C levels reviewed from their routine medical records

Full description

This study is a pragmatic, single-centre, parallel-group randomized controlled trial evaluating the integration of social prescribing into primary care for older adults with diabetes who experience loneliness. The intervention is delivered within an academic family health team and leverages existing interprofessional resources to address social determinants of health as part of routine clinical care.

Potential participants will be identified through electronic medical record (EMR) queries and clinic-based outreach. Loneliness screening will be conducted using the three-item UCLA Loneliness Scale (UCLA-3), administered via a secure electronic platform (REDCap). A flexible consent process, including both electronic and verbal options, will be used to accommodate varying levels of digital literacy within the target population.

Following enrolment, participants will be assigned to study arms using simple randomization (coin toss). The intervention consists of a structured referral to a primary care social worker. The social worker will conduct an initial assessment of the participant's social context, including social supports, barriers to engagement, and unmet practical needs. Based on this assessment, a co-developed plan will be implemented, which may include connection to community resources, facilitation of social engagement activities, and support addressing social or logistical barriers. Follow-up will be individualized in frequency and modality (in-person or virtual), reflecting a pragmatic, patient-centred approach.

Intervention delivery will not be protocolized beyond core components, in order to reflect real-world clinical practice. All social worker interactions will be documented within the EMR, allowing for characterization of intervention exposure (e.g., number and type of contacts). Participants in the comparator arm will continue to receive usual diabetes care during the study period, with access to social worker referral after study completion.

Study data will be collected through a combination of participant-reported measures and EMR-derived clinical data. Data will be stored in REDCap using unique study identifiers, with linkage files maintained separately on secure, access-restricted servers. Analyses will use regression-based approaches to estimate between-group differences, adjusting for baseline values and relevant covariates.

This study is designed to evaluate the feasibility and effectiveness of incorporating social care into chronic disease management within primary care settings. Findings will inform the scalability and implementation of social prescribing interventions aimed at reducing loneliness and improving health outcomes among older adults.

Enrollment: 90 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Diabetes, lonely

Exclusion criteria

• Dementia, acute psychiatric or medical illness

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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90 participants in 2 patient groups

Continue primary care

Active Comparator group

Description:

Continue seeing primary care provider

Treatment:

Other: Continue Primary care

Intervention arm

Experimental group

Description:

Referral to see a social worker

Treatment:

Behavioral: Social worker referral to address loneliness