Hematologic Neoplasms Clinical Trial
Official title:
Comprehensive Frailty Assessment
Verified date | February 2018 |
Source | Ohio State University Comprehensive Cancer Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The purpose of this research study is to describe a patients' fitness before and after treatment (whether that treatment be chemotherapy or a transplant). Fitness is a way of measuring a patient's current quality of health. With surveys, questionnaires and blood tests, we hope to create a tool that will give a good picture of patients' ability to tolerate treatment. In the future, we hope to devise the best treatment for a patient based on their "fitness".
Status | Completed |
Enrollment | 111 |
Est. completion date | August 2017 |
Est. primary completion date | August 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - patients with a plasma cell dyscrasia AND/OR any patient receiving a stem cell transplant for a hematologic malignancy at The Ohio State University - at least 18 years of age Exclusion Criteria: - Any medical or psychiatric condition that would make it difficult for the patient to comply with study procedures. |
Country | Name | City | State |
---|---|---|---|
United States | The Ohio State University Hospital East | Columbus | Ohio |
Lead Sponsor | Collaborator |
---|---|
Ohio State University Comprehensive Cancer Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Overall survival | We will assess overall survival and the relationship of those measures to patients' functional, cognitive and psychosocial health. | enrollment to date of death up to two years post-enrollment | |
Primary | Change in Comprehensive Frailty Assessment | Responses to the Comprehensive Frailty Assessment will be assessed before and after treatment and changes will be evaluated. In transplant patients, this will be measured one year post transplant and in the non-transplant arm, this will be assessed after the second cycle of treatment. | up to 14 months | |
Secondary | Time to progression | We will assess time to progression for multiple myeloma patients and the relationships of those outcomes to patients' functional, cognitive and psychosocial health. | date of enrollment to date of documented clinical progression up to two years post-enrollment |
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