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Cancer related Fatigue Intervention

Cancer related Fatigue Intervention - CarFI

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00016034
Enrollment
172
Registered
2018-12-04
Start date
2018-10-12
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

oncological diseases C00-C97

Interventions

Group 1: 8-week yoga intervention, once a week for 1 h + single psychoeducation for 1,5h Group 2: single psychoeducation for 1,5h

Sponsors

Interdisziplinäres Zentrum Palliativmedizin Klinik und Poliklinik für Strahlentherapie Universitätsklinikum Würzburg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - oncological disease - noticeable fatigue screening - Ability to consent

Exclusion criteria

Exclusion criteria: - severe physical and/or psychological impairment - insufficient German language skills - Approach route >50km

Design outcomes

Primary

MeasureTime frame
The primary outcome of this study is fatigue. Fatigue is measured at the beginning, after the intervention and at the 6-month follow-up for the intervention group. The waiting control group completes the questionnaire 10 weeks after the basic assessment or before the yoga intervention. Fatigue is measured with EORTC QLQ-FA13 13 Items (European Organization for Research and Treatment of Cancer - Quality of Life Questionnaire - Fatigue; Weis et al. 2017). Fatigue is measured in 3 dimensions with 13 elements: Physically, emotionally and cognitively. There are four answer categories "not at all", "a little", "quite a lot" and "very much", coded with values from 1 to 4: According to the scales of the EORTC QLQ-C30, the FA13 results are converted into a range from 0-100. Higher values indicate a higher level of fatigue.

Secondary

MeasureTime frame
The following secondary endpoints are measured at the beginning, after the intervention and 6 months after the intervention. - Depression (PHQ9) - Quality of life (EORTC QLQ-C15-PAL) - Distress (distress thermometer) - Symptom burden (ESAS) - Sense of coherence (SOC L9)

Countries

Germany

Contacts

Public ContactTeresa Zetzl

Universitätsklinikum Würzburg

Zetzl_T@ukw.de0931 201 28855

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 1, 2026