Children with cancer and their families after active treatment: Analyses of biopsychosocial needs and implications for health care

Children with cancer and their families after active treatment: Analyses of biopsychosocial needs and implications for health care - FamKi-onko-V

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00025289

Enrollment

252

Registered

2021-07-12

Start date

2021-06-21

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

(Hemato-)oncological diseases during childhood

Interventions

Group 1: Pediatric patients with a (hemato-)oncological disease and their close famly members after active treatment

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: pediatric cancer patients and their families during follow-up care; self-report for children: child >=11 years, sufficient language skills, written consent for participation

Exclusion criteria

Exclusion criteria: - Patient’s age =18 Jahre - Missing consent to participate/refusal - insufficient language skills - too burdened for participation (pediatrician's assessment)

Design outcomes

Primary

Measure	Time frame
Primary Endpoint/Aim 1: Health care use (medical & psychosocial) Primary Endpoint/Aim 2: Psychosocial burden (QoL, Symptoms of depression & anxiety), supportive care needs	—

Secondary

Measure	Time frame
- Coping - Disease management - Reintegration & participation - Functional limitations - Satisfaction with health care	—

Countries

Germany

Contacts

Public ContactLaura Inhestern

Universitätsklinikum Hamburg-Eppendorf, Institut und Poliklinik für Medizinische Psychologie

l.inhestern@uke.de040 741057684

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 12, 2026