Comparing Different Methods for Collection of Comorbidity Data Per the HCT-CI

Sponsor
Fred Hutchinson Cancer Center (Other)
Overall Status
Completed
CT.gov ID
NCT03434561
Collaborator
National Heart, Lung, and Blood Institute (NHLBI) (NIH)
360
1
38.3
9.4

Study Details

Study Description

Brief Summary

Comorbidity assessment in the field of HCT might be a burden on the medical team at the clinic or the research staff. This research study aims to explore and validate new methods, Claims-based and patient questionnaire-based, as alternatives to the standard chart-based method in order to facilitate comorbidity coding. The study aims to save time and effort of medical personnel and to ensure the inclusion of comorbidity information in all clinical trials and outcome research studies in order to improve the accuracy of treatment decision-making, patient assignment to appropriate HCT strategy and hence HCT outcomes.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Studies have shown the importance of pre-transplant comorbidities in predicting mortality after allogeneic HCT.

    However, comorbidity assessment might be a burden on the medical team at the clinic or the research staff. This research study aims to explore and validate new methods as alternatives to the standard chart-based method in order to facilitate comorbidity coding. The study aims to save time and effort of medical personnel and to ensure the inclusion of comorbidity information in all clinical trials and outcome research studies in order to improve the accuracy of treatment decision-making, patient assignment to appropriate HCT strategy and hence HCT outcomes.

    This study will investigate two parallel approaches aimed at simplifying comorbidity assessment and thereby facilitating wide-spread use of the HCT-CI. Patient questionnaire-based and Claims-based methods will be tested as possible alternative to the Chart-based method. primary outcome is prediction of non-relapse mortality. It is expected that once this method of comorbidity coding is validated, it will benefit physicians in non-academic institutions and community clinics.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    360 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Comparing Different Methods for Collection of Comorbidity Data Per the Hematopoietic Cell Transplantation Comorbidity Index (HCT-CI)
    Actual Study Start Date :
    Mar 22, 2013
    Actual Primary Completion Date :
    Jun 1, 2016
    Actual Study Completion Date :
    Jun 1, 2016

    Outcome Measures

    Primary Outcome Measures

    1. Compare the rate of agreement on HCT-CI scores between 3 measures [2 years]

      3 measures: the questionnaire-based and the claims-based methods versus the chart-based method.

    Secondary Outcome Measures

    1. Assess the accuracy of predicting HCT outcomes and resource utilization (e.g., hospitalization) between the three methods of scoring [2 years]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients eligible for autologous or allogeneic HCT.

    • Able to speak and read English.

    • Willing and able to provide informed consent.

    • There is no restriction based on diagnosis, intensity of conditioning regimen, type of donor graft, degree of HLA-matching, or stem cell source.

    • Patients >20 years old

    • Access to a telephone for study-related communications.

    Exclusion Criteria:
    • HCT candidates who cannot read, write, or speak English.

    • Patients <20 years old

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Fred Hutchinson Cancer Research Center Seattle Washington United States 98109

    Sponsors and Collaborators

    • Fred Hutchinson Cancer Center
    • National Heart, Lung, and Blood Institute (NHLBI)

    Investigators

    • Principal Investigator: Mohamed Sorror, MD, Associate Member, Fred Hutch

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Fred Hutchinson Cancer Center
    ClinicalTrials.gov Identifier:
    NCT03434561
    Other Study ID Numbers:
    • 2650
    • 4R00HL088021-03
    First Posted:
    Feb 15, 2018
    Last Update Posted:
    May 30, 2018
    Last Verified:
    May 1, 2018
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Fred Hutchinson Cancer Center
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 30, 2018