Investigating the Equivalence of the EORTC QLQ-C30 and the QLQ-F17

NCT05479682 | Completed

• 1 other identifier: Z-2021-1709-7
• Study Type: observational
• Target: 2,672
• Locations: 1 country
• Sites: 1

Brief Summary

The EORTC QLQ-C30, a patient-reported outcome measure (PROM) that is available in 110 different languages, has been used in thousands of clinical cancer trials worldwide. The QLQ-C30 is composed of six functioning scales (including a measure for global quality of life), three symptom scales, and six single items. Researchers and regulatory bodies came up with the idea to construct a shortened EORTC questionnaire that solely consists of functioning scales and to use additional symptom items according to the side effect profile of the specific medication under investigation. This shortened form termed QLQ-F17 includes the Physical Functioning (PF), Role Functioning (RF), Emotional Functioning (EF), Cognitive Functioning (CF), and Social Functioning (SF) scales as well as the Global Health Status/Quality of Life (QL) scale in their original wording. This functioning questionnaire can be amended with symptom-specific items taken from the EORTC item library. This method provides a flexible and economic testing strategy that fits the demands of regulators and users in industry and academia. It is an open question, however, whether the QLQ-F17 is equivalent to the QLQ-C30 in terms of measurement properties. Based on empirical research on response biases and order effects, one might argue that elimination of the symptoms between RF and CF-Dyspnea (DY), Pain (PA), Fatigue (FA), Insomnia (SL), Appetite (AP), Nausea/Vomiting (NV), Constipation (CO), and Diarrhea (DI)-and of the Financial difficulties (FI) item between SF and QL may alter the manner in which subsequent items are completed. Thus, from a methodological point of view, it is essential to confirm the psychometric properties of the QLQ-F17 and to present evidence that scale values derived from the QLQ-F17 are equivalent to those of the QLQ-C30. Only in the case of equivalence may studies using either of the two basic questionnaires be compared directly. The present project is designed to address this research question. This is an international multicenter survey study that will include respondents with cancer from Australia, Finland, France, Germany, Italy, Poland, Romania, Spain, Sweden, and United Kingdom. A randomized cross-over design will be applied, enabling between-patients as well as within-patients comparisons of the QLQ-C30 and the QLQ-F17. One group of respondents will first fill in the QLQ-C30 followed by the QLQ-F17, the other group will start with the QLQ-F17 followed by the QLQ-C30. A sample size of 1.500 cancer patients is sufficient to get precise estimates with narrow confidence intervals regarding item and scale-level agreement. Thresholds and margins to be used for the analyses in this study will be consented by a statistical advisory group. Reliability and psychometric properties can also be precisely estimated with a sample of this size. The present study is based on the hypothesis that the QLQ-F17 and the QLQ-C30 questionnaires are equivalent.

Conditions

Cancer; Quality of Life

Outcome Measures

Primary Outcomes (2)

• QLQ-C30

  The EORTC Core Questionnaire (QLQ-C30) includes six clearly distinguishable functioning scales that have been thoroughly tested and validated on an international level and that are available in 110 different language versions

  Day 1

• QLQ-F17

  The QLQ-F17 is the shortened version of the QLQ-C30 that is composed solely of items related to functioning, which include Physical (PF), Role (RF), Emotional (EF), Cognitive (CF) and Social Functioning (SF) scales as well as the Global Health Status/Quality of Life (QL) scale in their original wording.

  Day 1

Study Arms (2)

EORTC QLQ-C30 first, EORTC QLQ-F17 second

Intervention relates to the order of questionnaires to be completed. In this cohort, the EORTC QLQ-C30 will be completed first and after a short interim task the QLQ-F17 second.

EORTC QLQ-F17 first, EORTC QLQ-C30 second

Intervention relates to the order of questionnaires to be completed. In this cohort, the order of questionnaires is reversed: EORTC QLQ-F17 will be completed first and after a short interim task the QLQ-C30 second.

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

The sample will include patients with the following diagnoses: Breast, Lung, Colorectal, Prostate, Head\&Neck, Melanoma, Haematological, others The sample will include patients with the following treatment states: Active, Regular aftercare, Off (survivors, long-term survivors) The survey will be conducted in the following language regions: English-speaking countries: UK, US, Australia; West-Germanic language: German; Scandinavian language: Swedish; Slavic languages: Polish; Romance languages: French (France), Italian, Spanish (Spain), Romanian; Other European language: Finnish

You may qualify if:

• Patients suffering from cancer or in remission

You may not qualify if:

• none

Sponsors & Collaborators

• University Hospital Regensburg: lead
• European Organisation for Research and Treatment of Cancer - EORTC: collaborator
• Kantar Health: collaborator

Study Sites (1)

Center for Clinical Studies, University Hospital Regensburg

Regensburg, Germany

Location

Related Publications (1)

• Zeman F, Giesinger JM, Pukrop T, Petersen MA, Groenvold M, Nolte S, Kulis D, Shrestha S, Leysen L, Cocks K, Coens C, Ioannidis G, Pompili C, Koller M; of the EORTC QLG. The EORTC QLQ-F17 as a shortened version of the EORTC QLQ-C30 to assess self-reported functioning in cancer patients: investigating equivalence and psychometric properties in a randomized cross-over trial. EClinicalMedicine. 2025 Jun 3;84:103262. doi: 10.1016/j.eclinm.2025.103262. eCollection 2025 Jun.

  PMID: 40521164 DERIVED

MeSH Terms

Conditions

Neoplasms

Study Officials

• Michael Koller, Prof. Dr.

  Head of Center for Clinical Trials

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: CROSS SECTIONAL
• Target Duration: 1 Day
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Head of Center for Clinical Studies

Study Record Dates

• First Submitted: July 26, 2022
• First Posted: July 29, 2022
• Study Start: February 15, 2023
• Primary Completion: March 30, 2023
• Study Completion: March 30, 2023
• Last Updated: May 9, 2023

Record last verified: 2023-05

Data Sharing

• IPD Sharing: Will not share

Locations

DE (1)