Addressing Social Determinants of Health Among Metro Detroit Cancer Survivors

Barbara Ann Karmanos Cancer Institute

Status: Enrolling

Conditions: Cancer Survivors; Neuroendocrine Tumors; Cancer; Multiple Myeloma, Neoplasms; Gastrointestinal Cancers

Treatments: Other: Implementation of social determinants of health screening and referral

Study type: Interventional

Funder types: Other

Identifiers

NCT06908629

2024-042

Details and patient eligibility

About

The goal of this screening study is to determine the feasibility of completing a social needs screening tool in participants who have a past or current cancer diagnosis and reside in Metro Detroit, Michigan. Main questions to answer are:

• Can we have a completion rate of at least 80% of participants filling out the screening tool?
• Can we determine procedures for patient referrals based on social needs
• Can we implement brief interventions based on food access and digital inclusion (ensuring everyone has access to the digital technologies they need to participate in society)

Full description

In part 1 of the study, Participants will be administered a social screening tool either in person or via telephone. Responses to the screening tool will be translated into diagnosis codes which identify non-medical factors that may influence a patient's health status. In part 2 of the study, participants will be referred to community-based resources based on their responses to the social needs screening tool. Follow up will be made via telephone call at 2, 4, 6 and 8 weeks.

Enrollment: 120 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 18 years or older
• past or current cancer diagnosis
• reside in metropolitan Detroit (Wayne, Oakland, Macomb counties)
• English proficient
• Actively receiving care through one of Karmano's Cancer Institute's outpatient clinics OR post treatment survivors in the Detroit Research on Cancer Survivors (ROCS) longitudinal cohort study who have reported past food insecurity and agreed to be contacted for further research

Exclusion criteria

• none

Trial design

Primary purpose: Screening

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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120 participants in 1 patient group

Screening Needs Assessment

Experimental group

Treatment:

Other: Implementation of social determinants of health screening and referral