Validating Quality of Life Modules in Lymphoma

  • Research type

    Research Study

  • Full title

    An international field study for the reliability and validity of the Phase IV EORTC Quality of Life modules for patients with Hodgkin’s Lymphoma (EORTC QLQ-HL27), high-grade non-Hodgkin’s Lymphoma (EORTC QLQ-NHL-HG29), low-grade non-Hodgkin’s Lymphoma (EORTC QLQ-NHL-LG20), and Chronic Lymphocytic Leukaemia (EORTC QLQ-CLL17)

  • IRAS ID

    235255

  • Contact name

    Louise Enfield

  • Contact email

    louise.enfield@nhs.net

  • Sponsor organisation

    Netherlands Comprehensive Cancer Organisation

  • Duration of Study in the UK

    1 years, 11 months, 31 days

  • Research summary

    The aim of the project is to test the reliability and validity of four specific questionnaires that have been developed to assess the quality of life of lymphoma and chronic lymphocytic leukaemia (CLL) patients involved in clinical trials.

    The four specific questionaires have been developed to include symptoms, treatment related issues and any additional dimensions of quality of life specific to lymphoma and chronic lymphocytic leukaemia that are not sufficiently covered by the generic quality of life modules. The questionaires will be administered in combination with the generic EORTC QLQ−C30. The EORTC QLQ−C30 is a standardised questionnaire that has been developed by the European Organisation for Research and Treatment of Cancer (EORTC) that covers 30 mains symptoms and issues that may affect people with cancer.

    Patients will not directly benefit from participating, but in the long term we hope we will be able to offer better quality of care for all patients, because we will gain information on the quality of life and (long term) complaints of these survivors.

  • REC name

    London - City & East Research Ethics Committee

  • REC reference

    18/LO/1154

  • Date of REC Opinion

    19 Jul 2018

  • REC opinion

    Favourable Opinion