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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04049188
Other study ID # 00019460
Secondary ID 20181015
Status Recruiting
Phase N/A
First received
Last updated
Start date January 1, 2020
Est. completion date December 31, 2021

Study information

Verified date January 2020
Source Care Partners
Contact Andy Kyler, BSN, MBA
Phone 5036192621
Email andy.kyler@carepartners.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Feasibility study to report on the impact of ACCESS of single-fraction radiation therapy on cancer patients with bone metastases enrolled in hospice care.


Description:

Hospice care for terminally ill patients with metastatic cancer improves quality of life, pain control, and potentially also survival when patients are enrolled early.1-3 However, hospice programs are often seen by patients and their caregivers as the last resort after exhaustion of all effective treatment options. The need to revoke active treatment (for all hospice patients with cancer outside of the VA system) discourages hospice enrollment.

This study aims to understand and analyze barriers to access specifically for short course palliative radiation therapy in cancer patients enrolled in hospice.


Recruitment information / eligibility

Status Recruiting
Enrollment 31
Est. completion date December 31, 2021
Est. primary completion date January 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria:

- Solid Tumor Malignancies and Multiple Myeloma with Bone Metastases and Associated Bone Pain Enrolled in Hospice

Exclusion Criteria:

- Decisionally-Impaired Subjects, Pregnant Women

Study Design


Related Conditions & MeSH terms


Intervention

Radiation:
Single-Fraction Palliative Radiation Therapy
All subjects will be undergo single-fraction palliative radiation therapy who have cancer and associated bone metastases and symptomatic bone pain.

Locations

Country Name City State
United States CarePartners Hillsboro Oregon

Sponsors (3)

Lead Sponsor Collaborator
Care Partners OHSU Knight Cancer Institute, Oregon Health and Science University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Opioid Use for Pain Management Opioid Dosage (mg/day) Through study completion, an average of 1 year
Secondary Improved Quality of Life Measures Questionnaires using Herth Hope Index, Timed Up and Go, and Edmonton Symptom Assessment Scale During study completion
Secondary Improved Activities of Daily Living Questionnaires using Hearth Hope Index, Timed Up and Go, and Edmonton Symptom Assessment Scale During study completion
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