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Clinical Trials/NCT02033928
NCT02033928CompletedNot Applicable

Comprehensive Frailty Assessment

Ohio State University Comprehensive Cancer Center1 site in 1 country111 target enrollmentStarted: April 2014Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
111
Locations
1
Primary Endpoint
Change in Comprehensive Frailty Assessment

Study Overview

Brief Summary

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".

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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.

Outcomes

Primary Outcomes

Change in Comprehensive Frailty Assessment

Time Frame: up to 14 months

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.

Secondary Outcomes

  • Time to progression(date of enrollment to date of documented clinical progression up to two years post-enrollment)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ashley Rosko

Principal Investigator

Ohio State University Comprehensive Cancer Center

Study Sites (1)

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