Psychometric Properties of the Fear of Progression Questionnaire for Children in Two German Samples (Acute Treatment and Follow-Up Care)

Publikation: Beitrag in Fachzeitschrift › Forschungsartikel › Beigetragen › Begutachtung

Beitragende

  • Florian Schepper - , Universität Leipzig (Autor:in)
  • Anja Santel - , Elternhilfe für krebskranke Kinder Leipzig e.V. (Autor:in)
  • Jessy Herrmann - , Elternhilfe für krebskranke Kinder Leipzig e.V. (Autor:in)
  • Kristina Herzog - , Elternhilfe für krebskranke Kinder Leipzig e.V. (Autor:in)
  • Leonard Konstantin Kulisch - , Ruhr-Universität Bochum, Deutsches Zentrum für Psychische Gesundheit (DZPG) - Standort Bochum / Marburg (Autor:in)
  • Jörn-Sven Kühl - , Universität Leipzig (Autor:in)
  • Julia Martini - , Klinik und Poliklinik für Psychiatrie und Psychotherapie (Autor:in)

Abstract

BACKGROUND: Fear of progression (FoP) is among the most prevalent psychosocial burdens in paediatric oncology. Empirical evidence suggests that FoP is particularly pronounced during acute treatment and often persists into follow-up care. It is associated with heightened perception of physical symptoms, increased post-traumatic stress symptoms, more negative illness perceptions, and reduced quality of life (QoL). Consequently, a comprehensive diagnostic instrument is essential to assess FoP in children with cancer.

OBJECTIVE: This study aimed to prospectively validate the German self-report version of the Fear of Progression Questionnaire for Children (FoP-Q-SF/C) aged 7-18 years both during acute treatment and in follow-up care.

METHODS: A total of 116 children participated in the study, including 39 undergoing acute treatment and 77 in follow-up care. Participants completed the FoP-Q-SF/C. Factor analyses were conducted, and associations between FoP and QoL, illness perceptions, posttraumatic stress symptoms, time since diagnosis, cancer type and treatment modality were examined.

RESULTS: All items were applicable in children. The FoP-Q-SF/C demonstrated high internal consistency and good convergent, criterion and divergent validity. Consistent with previous research, factor analysis supported a one-factor structure, although findings suggest potential for structural refinement.

CONCLUSIONS: The FoP-Q-SF/C is a reliable and valid questionnaire for assessing FoP in children with cancer across different treatment phases. It serves as a valuable screening instrument to identify children at risk for elevated psychosocial distress and to guide targeted psychosocial interventions.

Details

OriginalspracheEnglisch
Aufsatznummere70254
Seitenumfang9
FachzeitschriftPsycho-oncology
Jahrgang34
Ausgabenummer8
PublikationsstatusVeröffentlicht - Aug. 2025
Peer-Review-StatusJa

Externe IDs

PubMedCentral PMC12350204
Scopus 105013204514
ORCID /0000-0003-2902-0171/work/204618456

Schlagworte

Ziele für nachhaltige Entwicklung

  • SDG 3 – Gute Gesundheit und Wohlergehen - Adolescent, Child, Disease Progression, Factor Analysis, Statistical, Fear/psychology, Female, Follow-Up Studies, Germany, Humans, Male, Neoplasms/psychology, Prospective Studies, Psychometrics, Quality of Life/psychology, Reproducibility of Results, Self Report, Stress Disorders, Post-Traumatic/psychology, Surveys and Questionnaires/standards, questionnaire, screening, oncology, fear of progression, children, validation, psychometrics, factor analysis, cancer, quality of life

Schlagwörter

  • Adolescent, Child, Disease Progression, Factor Analysis, Statistical, Fear/psychology, Female, Follow-Up Studies, Germany, Humans, Male, Neoplasms/psychology, Prospective Studies, Psychometrics, Quality of Life/psychology, Reproducibility of Results, Self Report, Stress Disorders, Post-Traumatic/psychology, Surveys and Questionnaires/standards, questionnaire, screening, oncology, fear of progression, children, validation, psychometrics, factor analysis, cancer, quality of life