QoL-MM: Quality of Life the Danish Multiple Myeloma Patients

Sponsor
Odense University Hospital (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT02892383
Collaborator
Danish Myeloma Study Group (Other)
800
10
106.1
80
0.8

Study Details

Study Description

Brief Summary

The aim of the project is to improve quality of life for multiple myeloma patients in the future.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Multiple myeloma is an incurable malignancy of the bone marrow and the second most common type of haematological cancer. In Denmark, about 320 patients are diagnosed annually with multiple myeloma, and the cancer often affects older people, but 30 % of the patients living with MM are of working age. The prognosis has improved markedly over the last two decades and is expected to improve further.

    Systematic monitoring of symptoms, side effects and complications over time outside clinical trials has not been performed yet. Knowledge of the elderly and frail patients´ perspective on the multiple myeloma disease is lacking, and the time after anti-myeloma treatment is left unstudied. A common side effect (up to 55 %) to specific types of anti-myeloma drugs is peripheral neuropathy (nerve injury), which can be temporary or permanent in the form of long-term sequelae of pain and numbness. Information on this side effect from the patients´ perspective is missing.

    The design of the project is a prospective, population-based, national, longitudinal survey with retrospective data collection from more Danish registers. We will include 800 previously untreated and relapsed multiple myeloma patients at treatment-demanding disease recruited from all Danish haematological departments. At inclusion, demographic data and patient-related prognostic markers will be obtained. The patients will complete four validated QoL instruments (EORTC QLQ-C30, MY20, CIPN20 and SF12v2) at 13 measuring points over a period of 24 months. The questions are concerning cancer and MM symptoms, peripheral neuropathy, other side effects, quality of life and functional capacity of a social, emotional and physical character.

    This project will provide real-time data collection of the symptoms, side effects, complications and quality of life from the general multiple myeloma patients´ perspective during and after anti-myeloma treatment. It will illuminate the reason for the patients´ high loss of working ability. The findings will be integrated in the future Danish National treatment guidelines, and recommendation for rehabilitation in aspects of shared decision making.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    800 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Quality of Life in Danish Multiple Myeloma Patients
    Actual Study Start Date :
    Feb 27, 2017
    Anticipated Primary Completion Date :
    Dec 31, 2023
    Anticipated Study Completion Date :
    Dec 31, 2025

    Outcome Measures

    Primary Outcome Measures

    1. A longitudinal description of quality of life (QoL) using patient-reported outcomes measurement (PROM) for the general population of multiple myeloma patients. [24 months]

      a. Description of changes in QoL over time

    Secondary Outcome Measures

    1. Description of changes in QoL over time, based on PROM for the general population of multiple myeloma patients. [24 months]

      To analyse changes in QoL measured by EORTC QLQ-C30 (score 0-100), EORTC QLQ-MY20 (score 0-100) and SF12v2-4-week recall (score 0-100) in relation to disease characteristics: ISS I-III Type/-s of anti-myeloma treatment Side-effects of treatment measured by EORTC QLQ-MY20 (score 0-100) and EORTC QLQ-CIPN20 (score 0-100) Quality of response: IMWG criteria for first and second line treatment To analyse changes in QoL measured by EORTC QLQ-C30 (score 0-100), EORTC QLQ-MY20 (score 0-100) and SF12v2-4-week-recall (score 0-100) in relation to patient characteristics: Myeloma Frailty score (fit, intermediate-fitness and frail) Karnofsky Performance score scale (0-100%) Charlson comorbidity Index (0-33) and Freiburger comorbidity index (0-3)

    2. Description of the impact of peripheral neuropathy on QoL in the general population of multiple myeloma patients over time, based on PROM. [24 months]

      To analyse changes in peripheral neuropathy measured EORTC QLQ-CIPN20 (score 0-100) in relation to Type/-s of anti-myeloma treatment Side effect of treatment measured by EORTC QLQ-MY20 (score 0-100). Quality of response: IMWG criteria for first and second line treatment To analyse changes in peripheral neuropathy measured by EORTC QLQ-CIPN20 (score 0-100) in relation to - Myeloma frailty score (fitness, intermediate-fitness and frail)

    3. Description of the impact of recalibration response shift for interpretation of data from longitudinal QoL studies using PROM for QoL measurement in the general population of previously untreated multiple myeloma patients. [9 months]

      Recalibration response shift is a change in the patients internal standard of Measurement and will be measured at a then-test interview 9 months after baseline. Then-test is a retrospective pre-test and will capture recalibration response shift and the true change in QoL. For the pre-test, post-test and then-test the EORTC QLQ-C30 (score 0-100), EORTC QLQ-MY20 (score 0-100), EORTC QLQ-CIPN20 (score 0-100) and SF12v2-4-week recall (score 0-100) will be used.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 110 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Previously untreated or relapsed multiple myeloma patients AND

    • Treatment demanding multiple myeloma disease

    Exclusion Criteria:
    • Inability to understand the Danish language or

    • Psychic or mental illness that prevents the patient from answering the questions in the questionnaires.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Sygehus Sønderjylland Aabenraa Denmark
    2 Aalborg University Hospital Aalborg Denmark
    3 Aarhus University Hospital Aarhus Denmark
    4 Sydvestjysk Sygehus Esbjerg Denmark
    5 Herlev Hospital Herlev Denmark
    6 Hospitalsenheden Vest Holstebro Denmark
    7 Rigshospitalet København Denmark
    8 Odense University Hospital Odense Denmark
    9 Sjællands Universitetshospital Roskilde Denmark
    10 Vejle Sygehus Vejle Denmark

    Sponsors and Collaborators

    • Odense University Hospital
    • Danish Myeloma Study Group

    Investigators

    • Principal Investigator: Lene Kongsgaard Nielsen, MD, Quality of Life Research Centre, Haematological Department, Odense Univsersity Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Lene Kongsgaard Nielsen, Specialist in Haematology, Odense University Hospital
    ClinicalTrials.gov Identifier:
    NCT02892383
    Other Study ID Numbers:
    • QoL-MM_OUH
    First Posted:
    Sep 8, 2016
    Last Update Posted:
    Feb 14, 2022
    Last Verified:
    Feb 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 14, 2022