C50: Malignant neoplasm of the breast
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: For all groups: • A history of breast cancer in the family. • Good command of German (to complete the questionnaires). • Willingness to participate at all measurement points (t0, t1, t2, t3). • Written consent to participate in the study. Additionally for intervention groups: • Approval from the health insurance provider to participate in a preventive measure (Section 23 of the German Social Code, Book V). • Registration for one of the planned intervention types (individual treatment or family treatment). Additionally for the comparison group: • No participation in a preventive measure during the study period
Exclusion criteria
Exclusion criteria: Acute physical or mental health conditions that make it impossible to take part in the interviews. • Refusal to take part in the study or lack of consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Health-related quality of life (SF-12), assessed at T0 (baseline), T1 (post-intervention), T2 (12-week follow-up), and T3 (24-week follow-up). Comparison between family spa, individual spa, and control group without intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| Depression and anxiety (PHQ-4), T0–T3 Fatigue (FACIT-Fatigue), T0, T1, T3 Mindfulness (MAAS), T0, T1, T3 Perceived stress (PSS-10), T0–T3 Body image (Body Image Scale), T0, T1, T3 Post-traumatic growth / resources (ERI-12), T0, T2, T3 Relationship satisfaction (DAS-4), T0–T3 (including partners) Family relationship quality (EVOS), T0–T3 (including partners) Social support (BSSS), T0–T3 (including partners) Health literacy (HLS-EU-Q), T0, T2 (including partners) BMI (self-report), T0–T3 Social network structure (egocentric network analysis), T0, T1 | — |
Countries
Germany
Contacts
Universitätsklinikum Würzburg, Med. Klinik 2, Abt. Psychosomatik