Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Clinique Romande de Readaptation
Age
5–80
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
The healthy volunteer or legal representative has been informed and has signed the informed consent form
Age 18-80 or age 5-10 (women or men)
Weight below 137 kg
Height between 120 and 190 cm
Agree to comply in good faith with all conditions of the study and to attend all required training
The patient has been informed and has signed the informed consent form
Age 18-80 (women or men)
Weight below 137 kg
Height between 120 and 190 cm
Neurological/musculoskeletal diagnoses
Impairment of the lower extremities
Stable medical and physical condition as considered by the attending doctor or physician
Agree to comply in good faith with all conditions of the study and to attend all required training
Other (non-neurological) diagnoses, who require intense training of the lower extremities
The rehabilitation physician or doctor provides a final agreement whether the participant can train with the LEAP
You may not be if
Strong adipositas, which makes it not possible to adjust the harness to the anthropometrics of the participant
Bracing of the spinal column.
Severe joint contractures disabling or restricting lower limb movements
Instabilities of bones or joints, fractures or osteoporosis/osteopenia
Allergy against material of harness
Open skin lesions
Luxations or subluxations of joints that should be positioned in LEAP
Strong pain
Strong spontaneous movements like ataxia, dyskinesia, myoclonus\*
Instable vital functions like pulmonal or cardiovascular conditions
Uncooperative or aggressive behaviour
Severe cognitive deficits
Inability to signal pain or discomfort
Apraxia\*
Severe spasticity (Ashworth 4)
Severe epilepsy\*
Insufficient head stability
Infections requiring isolation of the patient
History of significant autonomic dysreflexia
Systemic malignant disorders
Cardiovascular disorders restricting physical training
Peripheral nerve disorders
Other anatomic or co-morbid conditions that, in the investigator's opinion, could limit the patient's ability to participate in the study or to comply with follow-up requirements, or impact the scientific soundness of the study results.
Known or suspected non-compliance, drug or alcohol abuse,
Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant,
Participation in another study with investigational drug within the 30 days preceding and during the present study
Previous enrolment into the current study Contraindications marked with an \* are relative contraindications. Final approval needs to be obtained from the attending medical doctor.
