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Clinical Trials in Canada / NCT06973655
Recruiting Not applicable

Trial of Social Work Services in Fracture Clinic Setting

NCT06973655 · tracked via the Priya Life Science Canada tracker
Sponsor
Sheila Sprague
Phase
Not applicable
Started
2025-10-06
Last updated
2025-12-10

Condition(s) studied

Orthopaedic FracturesSocioeconomic Factors

Investigational drug(s) / intervention(s)

Social Work support

Social Work support: Participants enrolled during the treatment phase at their clinic will receive social work support for 6 months from the time of enrollment. They will have an intake appointment with the social worker before or during their initial fracture clinic visit to assess their needs, identify goals that they can address with the support of the social worker, and collaboratively formulate a personalized care plan tailored to their specific circumstances. The social worker will then implement the plan, which may involve educating participants and their support network, coordinating delivery of care and benefits, making referrals to community services, advocating for the participant, and providing emotional support and brief counselling. The social worker will be accessible to participants for 6 months post-enrollment, following up via telephone, telemedicine or in-person to evaluate the effectiveness of the care plan and offer sustained ongoing support.

Study summary

Every year, many Canadians sustain a fracture that requires surgical treatment and results in a long recovery period. During this recovery period, patients may experience new or worsening mental health issues including depression, anxiety, or post-traumatic stress disorder. Additionally, patients may experience new or worsening social and financial problems, such as food and housing insecurity, due to being unable to work or take care of other daily responsibilities. Current care for fracture patients is focused on treating their physical injuries and overlooks these other challenges. To address this gap in care, the investigators propose having a social worker available in the fracture clinic to provide patients with support beyond the care of their physical injury.

The investigators propose a trial of 2,000 patients to determine if social worker support improves recovery for patients after a serious fracture by reducing the number of times they return to the emergency room or urgent care centre. This trial will also determine if social work support improves patients' mental health, financial security, ability to work, and level of satisfaction with the care they receive, and whether it reduces the amount of opioid medication they use and number of missed visits during their recovery. Patients will be randomly assigned to receive either support from a social worker or usual care. For patients assigned to receive social worker support, the social worker will assess their individual needs and provide support, information, and referrals to social support services. The social worker will continue to support patients for up to one year after they join the trial. Patients will complete questionnaires at enrollment and at 6 weeks and 3, 6, 9, and 12 months after enrollment.

If this trial shows that support from a social worker in the fracture clinic during their recovery period is beneficial to patients who have experienced a serious fracture requiring surgery, it has the potential to change care for patients who experience these potentially life-changing injuries.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
The inclusion criteria are: 1. Aged 18 or older. 2. Has fracture of the appendicular skeleton 3. Fracture required surgical management. 4. Fracture occurred within the past 12 weeks. 3\. Willing to comply with the protocol. 4. Willing to provide informed consent. Exclusion Criteria: 1. Incarceration. 2. Expected injury survival of less than 6 months. 3. Terminal illness with expected survival of less than 6 months. 4. Currently enrolled in a trial that does not permit co-enrollment. 5. Unable to engage in protocol in the languages available in the local cluster. 6. Prior enrollment in the trial. 7. Declined to provide informed consent. 8. Not approached at (or prior to) the first post-surgery fracture clinic visit (missed participant). 9. Other reason to exclude the patient, as approved by the Methods Centre.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Zuckerberg San Francisco General Hospital and Trauma Centre San Francisco California Recruiting
Hamilton Health Sciences - Hamilton General Hospital Hamilton Ontario Not Yet Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06973655 on ClinicalTrials.gov ↗ ← All trials in Canada