Validation of the European Oncology Quality of Life Toolkit

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorFondazione IRCCS Istituto Nazionale dei Tumori, Milano

About this trial

The improvement or preservation of quality of life (QoL) is one of the three pillars of the European Union (EU) Mission on Cancer, which underpins the needs of patients from cancer diagnosis throughout treatment, survivorship, and advanced terminal stages. Clinical studies and real-world data show that the use of Patient Reported Outcome Measures (PROMs) for QoL assessment in routine oncology practice has positive effects on patient wellbeing and healthcare resource utilization. However, full implementation of PROMs is not yet part of standard of care and is not adequately considered in cancer policies and programs.

A comprehensive tool incorporating the perspective of patients at different stages of the disease trajectory and widely applicable across Europe is still lacking.

The European Oncology Quality of Life Toolkit (EUonQoL-Kit) is a unified patient-centred tool for the assessment of QoL, developed from preferences and priorities of people with past or current cancer experience. The EUonQoL-Kit includes three electronic questionnaires, specifically designed for different disease phases (patients in active treatment, survivors, and patients in palliative care), available in both static and dynamic (Computer Adaptive Testing, CAT) versions and in several European languages.

This is a multicentre observational study, with the following aims:

* The primary aim is to perform the psychometric validation of the EUonQoL-Kit. * Secondary aims are to assess its acceptability, to validate the static and dynamic versions against each other, and to provide estimates of QoL across European countries.

The EUonQoL-Kit will be administered to a sample of patients from 45 European cancer centres. The sample will include patients in active treatment (group A), survivors (group B), and patients in Palliative Care (group C).

Each centre will recruit 100 patients (40 from group A, 30 from group B, 30 from group C), for an overall sample size of 4,500 patients (at least 4,000 patients are assumed to be enrolled, due to an expected lower recruitment rate of 10-15%). Three sub-samples of patients (each corresponding to 10% of the total sample for each centre) will fill in an additional questionnaire:

* FACT-G (Functional Assessment of Cancer Therapy - General) and EQ-5D-5L (5-level European Quality of Life Five Dimension), to test concurrent validity. * Live-CAT version, to validate the static and dynamic versions against each other. * EUonQoL-Kit, at least 1 hour after the first completion, to assess test-retest reliability.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 18 years or more.

Present or past histologically confirmed diagnosis of solid tumour or haematological malignancy.

Being in one of these three conditions: A) Patients in active treatment; B) Survivors; C) in Palliative Care.

Native tongue or fluent in the language of the questionnaire

Disqualifiers

Cognitive impairment preventing the completion of the questionnaire

Trial population

Patients in one of the following three conditions will be screened for their eligibility: A) In active treatment: Undergoing or recently completed curative treatment for early-stage cancers OR undergoing or recently completed non-curative treatment for ad-vanced or metastatic cancers, including disease controlling/life prolonging tumour-directed treatment. B) Survivors: Being disease-free without evidence of active cancer, and at least one year off active treatment (with the exception of long-term adjuvant hormonotherapy). C) Palliative Care (PC): patients with advanced cancers with projected prognosis \<12 months and ECOG ≥2 OR referred to a specialist palliative care team for symptom control. OR receiving non-curative systemic treatment or radiotherapy purely for symptom control.

Trial design

Design model

Other

Time perspective

Cross-sectional

Treatments tested in this trial

  • Administration of the EUonQoL-Kit - Active Treatment questionnaire

    Other intervention

    Electronic questionnaire to be administered to patients in active treatment.

  • Administration of the EUonQoL-Kit - Survivors questionnaire

    Other intervention

    Electronic questionnaire to be administered to cancer survivors.

  • Administration of the EUonQoL-Kit - Palliative Care questionnaire

    Other intervention

    Electronic questionnaire to be administered to patients in palliative care.

Treatment groups

4,000 Participants
are divided into 3 treatment groups
Group A: A) EUonQoL-Kit - Active Treatment module1 intervention
Group B: B) EUonQoL-Kit - Survivors module1 intervention
Group C: C) EUonQoL-Kit - Palliative Care module1 intervention

Trial outcomes

Primary outcomes

1

Validity and reliability of the EUonQoL-Kit static version

Exploratory and confirmatory factor analyses, distribution of the scales' scores, reliability in terms of internal consistency and reproducibility, concurrent and construct validity, differential item functioning.

Time frame
All assessments at time of administration of the questionnaires, apart reproducibility that will be assessed with a re-test at least after 1 hour for all patients

Secondary outcomes

1

Acceptability of the EUonQoL-Kit

Acceptability of the EUonQoL-Kit and reasons for refusal, including patient burden in filling in the questionnaire

Time frame
At day 1
2

Validation of the EUonQoL-Kit dynamic (CAT) version

Comparison of the scores obtained with the static and dynamic versions to test if they produce similar, interchangeable results; assessment to test whether the items selected for the static version and the related CAT-settings should be adjusted to obtain optimal assessment.

Time frame
At day 1
3

Assessment of Quality of Life (QoL) inequalities across clusters of European populations, countries, and healthcare systems, using EUonQoL-Kit questionnaires

Analysis of the QoL scores (dependent variable) according to individual-level variables as well as country/health system level variables (independent variables)

Time frame
At day 1
4

Socio-demographic and clinical factors potentially associated with QoL

Assessment of QoL disparities across different patient groups (by gender, ethnicity, religion, area, psychological and socio-economic factors, and education level)

Time frame
At day 1

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Fondazione IRCCS Istituto Nazionale dei Tumori, Milano

Lead sponsor

Gustave Roussy, Cancer Campus, Grand Paris

Collaborator

German Cancer Research Center

Collaborator

Oslo University Hospital

Collaborator

The Netherlands Cancer Institute

Collaborator

Hospital del Mar Research Institute

Collaborator

Istituto Europeo di Oncologia

Collaborator

European Organisation for Research and Treatment of Cancer - EORTC

Collaborator

UNICANCER

Collaborator

EAPC

Collaborator

Institut Curie

Collaborator

EUROPEAN CANCER ORGANISATION

Collaborator

DIGICORE/IFO

Collaborator

Istituto Nazionale Tumori IRCCS - Fondazione G. Pascale

Collaborator

Alleanza Contro il Cancro

Collaborator

Istituti Fisioterapici Ospitalieri

Collaborator

STICHTING NEDERLANDS INSTITUUT VOOR ONDERZOEK VAN DE GEZONDHEIDSZORG

Collaborator

University of Milan

Collaborator

SporeData OÜ

Collaborator

ORGANISATION OF EUROPEAN CANCER INSTITUTES

Collaborator

FEDERAZIONE ITALIANA DELLE ASSOCIAZIONI DI VOLONTARIATO IN ONCOLOGIA

Collaborator

Medical University Innsbruck

Collaborator

SDRUZHENIE ASOTSIATSIA NA PATSIENTITE SONKOLOGICHNI ZABOLYAVANIA I PRIYATELI

Collaborator

FEDERATIA ASOCIATIILOR BOLNAVILOR DE CANCER

Collaborator

University of Leeds

Collaborator

The Leeds Teaching Hospitals NHS Trust

Collaborator

Region Hovedstaden (Bispebjerg Hospital & Rigshospitalet)

Collaborator

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