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Clinical Trials/NCT02543541
NCT02543541
Completed
N/A

A Pilot Study of Structured Palliative Care for Patients Enrolled on Phase I Clinical Trials

Case Comprehensive Cancer Center1 site in 1 country132 target enrollmentOctober 25, 2015
ConditionsCancer

Overview

Phase
N/A
Intervention
Not specified
Conditions
Cancer
Sponsor
Case Comprehensive Cancer Center
Enrollment
132
Locations
1
Primary Endpoint
Average total FACT-G score
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The goal of this research study is to find out if providing patients who are enrolled in phase 1 clinical trials with structured supportive care will enable them to continue in the Phase 1 trial longer and improve their quality of life by reducing or treating side effects and by providing emotional and social support to the patient and family. The structured supportive or palliative care intervention will be provided by a team of trained specialists which include doctors, nurses, social workers and spiritual care providers. The supportive care team will provide treatment to address symptoms, such as pain or anxiety, caused by the cancer itself or from the treatment. The team can make referrals to other specialists. Such as psychologists or nutritionist, if needed, and can help arrange for services to address home care needs.

Detailed Description

Primary Objective(s): To assess symptoms, adverse events, duration on study, reason for study discontinuation, and quality of life among patients participating in phase I clinical trials who receive structured palliative care, and those who receive standard supportive care. Duration on study will serve as the primary objective for sample size determination. Secondary Objective(s): 1. To describe the quantity (e.g. hours), type, and cost of palliative care personnel services used by patients and caregivers receiving structured palliative care. Exploratory: 1. To compare adverse event profiles, duration on study, and quality of life between patients who receive structured palliative care and those receiving standard supportive care. 2. To compare caregiver burden and quality of life between the study arms.

Registry
clinicaltrials.gov
Start Date
October 25, 2015
End Date
January 10, 2019
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients must be enrolled in a Phase 1 clinical trial and be within 2 weeks of starting the experimental therapy or intervention.
  • Patients are eligible to enroll on this study with or without the enrollment of their caregiver.

Exclusion Criteria

  • Patients diagnosed with a hematologic malignancy.
  • Caregiver Inclusion Criteria:
  • Any caregiver is considered eligible for this study; The caregiver is the person identified by the patient as the one who provides the most regular physical and/or emotional support.
  • Caregivers must be willing to complete surveys at baseline and on monthly basis.
  • Caregiver Exclusion Criteria:
  • Caregivers who are solely professional, paid caregivers

Outcomes

Primary Outcomes

Average total FACT-G score

Time Frame: Up to 6 months

Measure patient quality of life

Average total MSAS score

Time Frame: Up to 6 months

Assessment of patient burden

Duration on Study

Time Frame: Up to 6 months

Measure of central tendency of the duration patients were on the phase I study. Duration on study will serve as the primary objective for sample size determination

Reason for study discontinuation (Patient reported outcome)

Time Frame: Up to 6 months

Measure of central tendency for why patients discontinued the phase I study. Patient reported outcomes for reason for study discontinuation will be qualitatively assessed

Adverse events

Time Frame: Up to 6 months

Measure of central tendency of adverse events. AE will be described and further categorized as modifiable (primary symptom experience) and non-modifiable (laboratory abnormalities). The influence of adverse events on study outcomes particularly duration on study and reason for study discontinuation will be assessed. An exploratory weighted adverse event score will be calculated using the equation: adverse event score = ∑ (NAE \* GAE) where N denotes the adverse event number, G denotes grade, AE denotes adverse event. These scores will be compared between study arms

Secondary Outcomes

  • Mean number of hours of palliative care services(Up to 6 months)
  • Type of palliative care services(Up to 6 months)

Study Sites (1)

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