not applicable (healthy) n/a (healthy)
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: • Between 18 and 35 or between 55 and 85 years of age • Able to provide informed consent
Exclusion criteria
Exclusion criteria: • Unable to follow simple instructions • Insufficient knowledge of the Dutch or English language to understand the purpose and methods of the study • Skin lesions at the thigh • Sensory impairments • Severe blood pressure fluctuations • Inability to sit in required posture in experiment chair for 60 minutes • Taking blood thinners or showing signs for increased bleeding tendency
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main study parameter is the level of discomfort as indicated continuously by the participants through a slider with a visual analogue scale. The scale reaches from no discomfort at all to maximum imaginable discomfort. A separate switch which releases all forces if activated by the participant is used to detect onset of pain. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary study parameters are the number of completed test sessions/dropouts, subject characteristics (height, weight, age, gender), records of observations of skin changes or other negative signs (directly after force application and several days after the session), and surface EMG recordings of the rectus femoris muscle. | — |
Countries
Netherlands