Occupational integration, everyday life management and well-being after childhood cancer

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00000731

Enrollment

400

Registered

2011-02-24

Start date

2008-09-11

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

childhood cancer

Interventions

Group 1: Screening study: no intervention

focus of analyses are relations among variables

see "endpoints" for assessed variables

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: cancer diagnosis in childhood, at time of study at least 18 years old, at least 5 years off therapy, signed informed consent

Exclusion criteria

Exclusion criteria: not able to read and write German

Design outcomes

Primary

Measure	Time frame
Primary outcomes are psychological well-being and coping. Main goals of the study are the assessment of psychological well-being (screening/description of study group) and the analysis of relations between different ways of coping and psychological well-being. Both endpoints are assessed at the same time. They are operationalized by the following questionnaires/items: Psychological Well-being: -Brief Symptom Inventory 18 (Derogatis 2000) -Posttraumatic Stress Diagnostic Scale, 8 Item Version (Ehring et al. 2007) Coping: -Cognitive Control Strategy Scale (Stam et al., 2006) -White Bear Suppression Scale (Wegner & Zanakos, 1994) -Illness Perception Scale-Revised (Moss-Morris et al., 2002) -Subjective Risk Perception -Perceived positive consequences/benefits	—

Measure

Time frame

Primary outcomes are psychological well-being and coping. Main goals of the study are the assessment of psychological well-being (screening/description of study group) and the analysis of relations between different ways of coping and psychological well-being. Both endpoints are assessed at the same time. They are operationalized by the following questionnaires/items: Psychological Well-being: -Brief Symptom Inventory 18 (Derogatis 2000) -Posttraumatic Stress Diagnostic Scale, 8 Item Version (Ehring et al. 2007) Coping: -Cognitive Control Strategy Scale (Stam et al., 2006) -White Bear Suppression Scale (Wegner & Zanakos, 1994) -Illness Perception Scale-Revised (Moss-Morris et al., 2002) -Subjective Risk Perception -Perceived positive consequences/benefits

—

Secondary

Measure	Time frame
Secondary outcome variables are sociodempgraphic information/social adaptation, medical late effects, general distress, social support, and body image. Secondary outcome variabels are assessed at the same time point as primary outcomes. The following questionnaires are used: -Questionnaire on sociodemographic and health information -Distress Thermometer (Holland & Reznik, 2005) -Questionnaire on Social Support, 14 Item Shortform (Fydrich, Sommer & Brähler, 2007) -Body Image Questionnaire (Wenninger et al., 2003)	—

Measure

Time frame

Secondary outcome variables are sociodempgraphic information/social adaptation, medical late effects, general distress, social support, and body image. Secondary outcome variabels are assessed at the same time point as primary outcomes. The following questionnaires are used: -Questionnaire on sociodemographic and health information -Distress Thermometer (Holland & Reznik, 2005) -Questionnaire on Social Support, 14 Item Shortform (Fydrich, Sommer & Brähler, 2007) -Body Image Questionnaire (Wenninger et al., 2003)

—

Countries

Germany

Contacts

Public ContactKerstin Wenninger

Universitätsklinikum Freiburg Zentrum für Kinder- und Jugendmedizin - Pädiatrische Hämatologie und Onkologie

kerstin.wenninger@uniklinik-freiburg.de+49 761 270-46340

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026