all patients during allogenic stemcelltransplantation C81-C96 D46
Conditions
Interventions
Group 1: Whole body vibration training
performed on a side-alternating oscillation platform (five times/ week, 20-25 min per
training session)
Group 2: Intervention consists of standard inpatient care
Sponsors
Universitätsklinik Freiburg, Klinik für Innere Medizin I
Eligibility
Sex/Gender
All
Age
16 Years to 80 Years
Inclusion criteria
Inclusion criteria: All patients eligible for alloHCT. All patients able to perform cardiopulmonary exercise test. Signed informed consent.
Exclusion criteria
Exclusion criteria: Instable bone metastases, epilepsy, endoprothesis in knee or hip, severe heart disease NYHA III-IV, pacemaker
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| phyiscal performance (VO2peak) at the time of discharge (T1) | — |
Secondary
| Measure | Time frame |
|---|---|
| - Physical performance (VO2peak) measured during cardiopulmonary exercise test on cycle ergometer 180 days after alloHCT - mobility und strength [cm;s;F] force platform (Leonardo Mechanograph®) -Maximum strength: maximum voluntary contraction (MVC) of knee extension and flexion (Contrex®) - gait speed and gait variability (Moticon, openGo®) - Thickness of the quadriceps femoris muscle [cm] Ultrasonography at midpoint of the thigh -Body composition (fat-free mass, body cell mass, phase angle) [(°; %)] - qualitiy of life and fatigue (EORTC QLQ C30; EORTC-QLQ_HDC29; MFI) -physical activity before and after diagnosis - FES-I questionnaire -Transplant-specific outcomes | — |
Countries
Germany
Contacts
Public ContactAntonia Pahl
Universitätsklinik Freiburg, Department Innere Medizin, Klinik für Innere Medizin I, Schwerpunkt Hämatologie, Onkologie und Stammzelltransplantation
Outcome results
None listed