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Embedded Palliative Care in Managing Symptoms in Participants With Recurrent Stage III-IV Thoracic Malignancies and Their Caregivers

Embedded Palliative Care in the Management of Advanced Thoracic Malignancies

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04662645
Enrollment
68
Registered
2020-12-10
Start date
2018-12-12
Completion date
2020-12-05
Last updated
2023-10-26

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

Conditions

Caregiver, Malignant Pleural Neoplasm, Metastatic Thymic Carcinoma, Recurrent Lung Carcinoma, Recurrent Thymic Carcinoma, Stage III Lung Cancer AJCC v8, Stage IIIA Lung Cancer AJCC v8, Stage IIIB Lung Cancer AJCC v8, Stage IIIC Lung Cancer AJCC v8, Stage IV Lung Cancer AJCC v8, Stage IVA Lung Cancer AJCC v8, Stage IVB Lung Cancer AJCC v8

Brief summary

This trial studies how well embedded palliative care works in managing symptoms in participants with stage III-IV thoracic malignancies that has come back and their caregivers. Embedded palliative care may improve distress and anxiety in participants and caregivers.

Detailed description

PRIMARY OBJECTIVES: I. To determine feasibility of embedding a palliative care (PC) physician within the James Thoracic Oncology Clinic. II. To assess patient and caregiver outcomes over a 12-month period within an embedded onco-palliative care clinic model. III. To evaluate and describe clinician attitudes and beliefs regarding utilization of embedded palliative care as well as symptoms of provider burnout. IV. To analyze health care utilization among participants receiving embedded onco-palliative care. OUTLINE: Participants and caregivers undergo embedded palliative care comprising symptom management (physical and psychological), advanced directives and goals of care discussion, caregiver support, and referral for adjunctive supportive services as needed at each clinic visit. After completion of study, patients are followed for up to 1 year.

Interventions

Undergo embedded palliative care

OTHERQuestionnaire Administration

Ancillary studies

Sponsors

Ohio State University Comprehensive Cancer Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with advanced or metastatic cancer of the chest (lung, thymus, or pleura): stage III or IV, recurrent disease * Patients will receive therapy (chemotherapy, immunotherapy, targeted therapy or radiation therapy) at The Ohio State University * New patients (defined as patients who have received no therapy for metastatic disease or have started treatment for metastatic disease within the last 30 days) or established patients with advanced cancer receiving anti-cancer therapy, no limit on prior therapies * Patient and caregiver must be able to read and understand consent form * Patients must designate a willing caregiver to participate although caregiver consent is not required for patient participation

Exclusion criteria

* Patients who are already enrolled or have been previously enrolled in palliative care or hospice services as an outpatient. Inpatient palliative care consultation prior to enrollment is permitted * Patients who do not qualify for active anti-cancer therapy and opt to enroll in hospice services prior to study enrollment * Patients who are unable to read or understand consent form * Patients receiving primary systemic treatment outside of Ohio State. Outside radiation therapy is permitted

Design outcomes

Primary

MeasureTime frameDescription
Health care utilization outcomesUp to 12 monthsWill be captured using Integrated Health Information Systems electronic medical record data as well as patient reported events.
Acceptance from providers to assess utilization of palliative care servicesUp to 12 monthsAcceptance will be evaluated utilizing provider surveys (to capture provider opinions on palliative care utilization) as well as rate of enrollment. Preliminary data will be summarized and collected. Confidence intervals will also be calculated for feasibility rates.
Demand of palliative care services to be evaluatedUp to 12 monthsPreliminary data will be summarized and collected. Confidence intervals will also be calculated for feasibility rates.
Capacity and productivity to be evaluatedUp to 12 monthsClinician capacity and productivity will be evaluated by looking at scheduling as well as billing productivity. Preliminary data will be summarized and collected. Confidence intervals will also be calculated for feasibility rates.
Resource assessment of staff and spaceUp to 12 monthsResources required, including patient care rooms and nursing support will also be evaluated. Preliminary data will be summarized and collected. Confidence intervals will also be calculated for feasibility rates.
Symptom burden (patient outcome) supportive care screenUp to 12 monthsWill be assessed using Supportive care screen.
Symptom burden (patient outcome) Functional Assessment of Cancer Therapy-LungUp to 12 monthsWill be assessed using Functional Assessment of Cancer Therapy-Lung
Symptom burden (patient outcome) using HADSUp to 12 monthsWill be assessed using Hospital Anxiety and Depression Scale (HADS)
Symptom burden using National Comprehensive Cancer Network distress thermometer (patient outcome)Up to 12 monthsWill be assessed using National Comprehensive Cancer Network distress thermometer
Anxiety assessment using Hospital Anxiety and Depression Scale (patient outcome)Up to 12 monthsAnxiety assessed using the Hospital Anxiety and Depression Scale
Depression assessment using Hospital Anxiety and Depression Scale (patient outcome)Up to 12 monthsDepression assessed using the Hospital Anxiety and Depression Scale
Functional status assessed using Functional Activities Scale (patient outcome)Up to 12 monthsFunctional status assessment using Functional Activities Scale (FAS)
Health care service needs assessed using Supportive Care Needs Survey Partners and Caregivers (SCNS- P and C) (Caregiver outcome)Up to 12 monthsCaregiver needs assessment using Supportive Care Needs Survey - Patients & Caregivers (SCNC-P&C)
Psychological/emotional needs assessed using SCNS- P and C (Caregiver outcome)Up to 12 monthsCaregiver needs assessment using Supportive Care Needs Survey - Patients & Caregivers (SCNC-P&C)
Work/social needs assessed using SCNS- P and C (Caregiver outcome)Up to 12 monthsCaregiver needs assessment using Supportive Care Needs Survey - Patients & Caregivers (SCNC-P&C)
Information needs assessed using SCNS- P and C (Caregiver outcome)Up to 12 monthsCaregiver needs assessment using Supportive Care Needs Survey - Patients & Caregivers (SCNC-P&C)
Self-reported barriers and attitudes regarding palliative care assessed using Ohio State Palliative Care Provider Survey (Provider outcome)Up to 12 monthsOhio State Palliative Care Provider survey used to assess perceived barriers to referral

Secondary

MeasureTime frameDescription
Challenges for patients, caregivers, and the treating oncologist in an embedded palliative care modelUp to 12 monthsevaluate the challenges for patients, caregivers and treating oncologist in embedded palliative care

Countries

United States

Outcome results

None listed

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