n.v.t. dit onderzoek betreft géén aandoening. not applicable
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: • Aged 55 to 75 years • Not meeting the Dutch Norm for Health-enhancing Physical Activity; the subject is not involved in >= 30 min of at least moderate-intensity aerobic physical activity on >= 5 days per week (assessed with physical activity questionnaire) • No participation in any structured or regular exercise training programs for the last 3 months.
Exclusion criteria
Exclusion criteria: • Allergic or sensitive for milk proteins, or lactose intolerant • Diagnosed with renal insufficiency • On a diet which affects protein intake (i.e. advices of an increase, decrease or type of protein (intake)) • Having known contraindications for exercise • Diagnosed with cancer for which currently treated • Having a contraindication to MRI scanning (including, but not limited to): * pacemakers and defibrillators * intraorbital or intraocular metallic fragments * ferromagnetic implants * claustrophobia • Participation in other intervention trial • Unable to understand Dutch • Having no general physician.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome of this study is the change in isometric quadriceps strength (Biodex). Quadriceps strength is measured at baseline, after 2 and after 4 weeks. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary parameters are changes quadriceps cross sectional area and volume (MRI and ultrasound), handgrip strength (dynamometer), power of the lower limb (chair rise time test), physical fitness (Åstrand-Rhyming test), habitual physical activity (accelerometer) and daily protein intake (24h recall questionnaire). Parameters are assessed at baseline, 2 weeks and 4 weeks. Habitual physical activity and protein intake will be assessed at baseline and after 4 weeks. | — |
Countries
Netherlands