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Multimodal therapy concept and aerobic training in breast cancer patients with chronic cancer-related fatigue syndrome (CRF): a comprehensive cohort design study

Multimodal therapy concept and aerobic training in breast cancer patients with chronic cancer-related fatigue syndrome (CRF): a comprehensive cohort design study - CRF-study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00003736
Enrollment
114
Registered
2012-06-19
Start date
2011-06-22
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

breast cancer patients with fatigue-syndrom G93.3

Interventions

Group 1: aerobic training, minimum 30 minutes, once a week, 10 interventions Group 2: multimodal therapy, minimum 30 minutes, once a week, 10 interventions Group 3: multimodal therapy + aerobic traini

Sponsors

Forschungsinstitut Havelhöhe (FIH)
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Not any chemotherapy, radiotherapy, surgery in the last 6 month. Final diagnosis from June 2009.

Exclusion criteria

Exclusion criteria: untreated cardiac, thyroid, nephric desease or untreated circulatory disorder

Design outcomes

Primary

MeasureTime frame
Cancer Fatigue Scale (CFS-D), german version: data collection: first intervention, last intervention, 6 months after last intervention Pittsburgh Sleep Quality Index (PSQI): data collection: first intervention, last intervention, 6 months after last intervention

Secondary

MeasureTime frame
Quality of life index with EORTC QLQ-C30, time of measurement: first intervention, last intervention, 6 months after last intervention. General vegetative status with Trait aR, time of measurement: first intervention, last intervention, 6 months after last intervention. Actual vegetative status with State aR, time of measurement: first intervention, last intervention, 6 months after last intervention. Anxiety and Depression with Hospital Anxiety and Depression Scale (HADS), time of measurement: first intervention, last intervention, 6 months after last intervention. Self-regulation with Scale of self-regulation, time of measurement: first intervention, last intervention, 6 months after last intervention. Internal coherence with ICS, time of measurement: first intervention, last intervention, 6 months after last intervention. Mental participation of eurythmics with Bewegung und innere Kongruenz (ICPH, Version 2.1), time of measurement: last intervention and 6 months after last intervention. Mental participation of drawing therapy with Innere Kongruenz und Einklang mit der Therapie (ICPTh, Version 1.0), time of measurement: last intervention and 6 months after last intervention. Physiologic measurements: rhythm of rest and activity with 72-hours-Aktimeter and 24-hours-ECG, time of measurement: 0-3 weeks before first intervention, 0-3 weeks after last intervention. Scales for therapists: erythmics: HFET-2, time of measurement: 0-3 weeks before first intervention, 0-3 weeks after last intervention. drawing therapy: AKT-DIAG, time of measurement: first intervention, 0-3 weeks after last intervention.

Countries

Germany

Contacts

Public ContactDanilo Pranga

Forschungsinstitut Havelhöhe (FIH)

dpranga@havelhoehe.de030 36501338

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 10, 2026