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Lay Health Worker Expanded Intervention in Community Oncology Practices

Lay Health Worker Expanded Intervention in Community Oncology Practices

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04463992
Enrollment
416
Registered
2020-07-09
Start date
2020-10-05
Completion date
2024-10-17
Last updated
2025-04-27

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

Conditions

Cancer, End of Life

Keywords

cancer end of life patient-centered

Brief summary

Undertreated patient symptoms and resulting acute care use require approaches that improve symptom-burden. Previously a lay health worker (LHW)-led symptom screening intervention was developed for patients with cancer. In pilot work, the intervention was associated with improvements in patient symptom burden and reductions in healthcare use and costs of care at the end of life. This intervention will be expanded across several clinics to evaluate the impact of the LHW intervention on with cancer and the LHW will be trained to refer patients to palliative care. This randomized intervention will evaluate the effect on healthcare use, total costs, palliative care and hospice referral.

Detailed description

All patients with newly diagnosed cancer, over the age of 75 will be randomized into the CareMore Pilot 2 Program with 200 randomized to the intervention grou and 200 randomized to the control group.

Interventions

The intervention is a 12-month telephonic program in which a lay health worker (LHW), supervised on-site by a registered nurse practitioner (RNP), assessed patient symptoms after diagnosis using the validated Edmonton Symptom The intervention is a 12-month telephonic program in which a lay health worker (LHW), supervised on-site by a registered nurse practitioner (RNP), assessed patient symptoms after diagnosis using the validated Edmonton Symptom Assessment Scale (ESAS) (cite) with the frequency of symptom assessment varying based on patient risk.

OTHERUsual Care

Usual care as provided by local oncologists

Sponsors

Stanford University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
TRIPLE (Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
75 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

* Newly diagnosed or relapsed cancer diagnosis. * 75 years or older * Diagnosis of relapse or progressive disease (any cancer diagnosis) as identified by imaging or biopsy and confirmed by physician. * Must have capacity to verbally consent

Exclusion criteria

* Inability to consent to the study due to lack of capacity as documented by the referring physician.

Design outcomes

Primary

MeasureTime frameDescription
% of patients with Emergency Department Visit within 12-months after patient enrollment (Chart Review)12 months after patient enrollmentEmergency Department use for each patient will be abstracted by electronic medical record chart review for each patient at 12 months after enrollment. We will evaluate comparisons of the % of patients with emergency department visits between study arms.
% of patients with Hospitalization Visits within 12 months after patient enrollment (Chart Review)12 months after patient enrollmentHospitalization use for each patient will be abstracted by electronic medical record chart review for each patient at 12 months after enrollment. We will evaluate comparisons of hospitalizations between the two study arms.

Secondary

MeasureTime frameDescription
% of patients with an Acute Care Facility Death (Chart Review)30 days prior to death for patients who died at 12-months follow-upAcute Care Facility Deaths for each patient will be abstracted by electronic medical record chart review and claims review for each patient who has died at 12-months followup. We will evaluate comparisons of Acute Care Facility Deaths between study arms.
% of patients with Emergency Department Visit in the last 30 days of life (Chart Review)30 days prior to death for patients who died at 12-months follow-upEmergency Department use for each patient will be abstracted by electronic medical record chart review for each patient who has died. We will evaluate comparisons of emergency department visits between study arms.
% of patients with a Hospice Consult within 12-months after patient enrollment (Chart Review)12 months after patient enrollmentHospice consult for each patient will be abstracted by electronic medical record chart review for each patient at 12 months after enrollment.
% of patients with a Hospice Consult in the last 30 days of life (Chart Review)30 days prior to death for patients who died at 12-months follow-upHospice use for each patient will be abstracted by electronic medical record chart review for each patient who has died. We will evaluate comparisons of hospice use between study arms.
Total Costs of Care (Claims Review)Time of enrollment to 12 months followup or death, whichever is firstTotal costs of care for each patient will be obtained through claims data for each patient for each patient who has died. We will evaluate comparisons of Total costs of care between study arms.
% of patients with Hospitalization Visits in the last 30 days of life (Chart Review)30 days prior to death for patients who died at 12-months follow-upHospital use for each patient will be abstracted by electronic medical record chart review for each patient who has died. We will evaluate comparisons of hospitalization use between study arms.
Total Health Care Costs (Claims Review)12 months after patient enrollmentTotal Health Care Costs for each patient will be abstracted by medical claims data review for each patient at 12 months after enrollment.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026