Evaluation and implementation of a multidisciplinary, standardized, guideline-based long-term follow-up care for today's adults, former children and adolescents with cancer in Germany - A prospective, multicenter, nationwide care study in the aftercare network (LE-Na)

Evaluation and implementation of a multidisciplinary, standardized, guideline-based long-term follow-up care for today's adults, former children and adolescents with cancer in Germany - A prospective, multicenter, nationwide care study in the aftercare network (LE-Na) - LE-Na

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00033303

Enrollment

5000

Registered

2024-02-05

Start date

2023-09-28

Completion date

Unknown

Last updated

2026-03-02

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

Conditions

Long-term follow-up care for former cancer patients by providing information on late effects and recording the prevalence of secondary diseases, including prospective records in a database

Interventions

Group 1: Fatique FA 12 at consultation: all RG at first presentation and after 5 years Distress Distress thermometer on presentation at the consultation: -> RG 1: at initial prese

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Diagnosis and treatment of an oncological disease in childhood or adolescence (before the 18th birthday) - Completed regular oncological aftercare (at least 5 years after the end of treatment of the primary oncological disease) - at least 6 months after completion of radiotherapy/chemotherapy, at least 12 months after completion of a stem cell transplant (e.g. in the case of relapses, secondary neoplasia) - Good understanding of the German language

Exclusion criteria

Exclusion criteria: - persons unable to give consent - already involved in interdisciplinary aftercare consultation in the past - currently undergoing oncological therapy

Design outcomes

Primary

Measure	Time frame
Primary target variables (work package 2a and 4): - Satisfaction with the care offered after three years - Health-related self-efficacy expectations after three years	—

Secondary

Measure	Time frame
Secondary objectives: - Implementability of guideline recommendations in the specialized centers participating in the project - Health-related quality of life after three years - Recruitment success, differentiated by gender - Incidence of late effects - Sensitivity of questionnaire-based psychosocial screening in comparison to interview-based psychosocial anamnesis	—

Countries

Germany

Contacts

Public ContactJudith Gebauer

UKSH Lübeck

judith.gebauer@uksh.de0451- 500 44195

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 14, 2026