- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04820894
Perception of Cure Among Patients With Metastatic Cancer
The Perception of Cure Among Patients With Metastatic Cancer
Study Overview
Status
Intervention / Treatment
Detailed Description
PRIMARY OBJECTIVE:
I. To assess the proportion of patients with metastatic cancer who anticipate cure before starting immunotherapy.
SECONDARY OBJECTIVES:
I. To determine if expectations of cure are associated with quality of life and distress.
II. To determine if patients' perceptions differ by gender, age, and ethnicity.
OUTLINE:
Patients complete surveys over 30 minutes about sociodemographic information and perception of immunotherapy, over 10 minutes about expectations of cure, over 10 minutes about anxiety, over 10 minutes about depression, and over 30 minutes about physical well-being. Patients' medical records are reviewed.
Study Type
Contacts and Locations
Study Locations
-
-
California
-
Duarte, California, United States, 91010
- City of Hope Medical Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Eligibility Criteria:
- Patients must be aged 18 and over
- Patients sufficiently fluent in English
- Patients must have a cytologically or pathologically verified diagnosis of cancer
- Patients must have measurable metastatic disease
- Patients must be initiating immunotherapy
- Patients must be undergoing evaluation and treatment at City of Hope Cancer Center
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Observational (survey, medical records review)
Patients complete surveys over 30 minutes about sociodemographic information and perception of immunotherapy, over 10 minutes about expectations of cure, over 10 minutes about anxiety, over 10 minutes about depression, and over 30 minutes about physical well-being.
Patients' medical records are reviewed.
|
Complete surveys
Medical records are reviewed
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Percentage of patients
Time Frame: Up to 2 years
|
Will assess the percentage of patients who anticipate cure before starting immunotherapy, scoring a '1' on the Perception of cure tool, and anticipate >75% chance for a cure.
|
Up to 2 years
|
Patient Reported Outcomes Measurement Information System (PROMIS)
Time Frame: Up to 2 years
|
Descriptive analyses (e.g.
frequency statistics) will be used to characterize the sample and to look at the association between Patient Reported Outcomes Measurement Information System (PROMIS) tool score with perception of cure score.
|
Up to 2 years
|
Functional Assessment of Cancer Therapy-General (FACT-G)
Time Frame: Up to 2 years
|
Descriptive analyses (e.g.
frequency statistics) will be used to characterize the sample and to look at the association between Functional Assessment of Cancer Therapy-General (FACT-G) overall score with perception of cure score.
|
Up to 2 years
|
Perceptions of cure
Time Frame: Up to 2 years
|
Chi-square analyses will be used to examine perceptions of cure by sociodemographic characteristics: gender (male and female), age (< 60 and > 60), and ethnicity (white non-Hispanic, Hispanic, and other). |
Up to 2 years
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 19322 (Other Identifier: City of Hope Medical Center)
- P30CA033572 (U.S. NIH Grant/Contract)
- NCI-2021-01818 (Registry Identifier: CTRP (Clinical Trial Reporting Program))
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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