movement rotation
Conditions
Interventions
None listed
Sponsors
Reinier de Graaf Groep
Eligibility
Age
2 Years to 17 Years
Inclusion criteria
Inclusion criteria: In order to be eligible to participate in this study, a subject must meet all of the following criteria: - all patients in the outbound clinic of trauma/ orthopedics after lower arm trauma after the cast has been removed - patients approval for inclusion in the clinical study - sufficient command of the Dutch language - Age >4yr-16yr
Exclusion criteria
Exclusion criteria: - arm still in cast/ pressure band aid
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main study parameter is the pro- and supination range of motion of the arm as measured by the PROSUP mobile phone application (index) and the goniometer (reference). The outcome will be expressed as degrees. Accuracy; Criterion validity: correlation between *smartphone with app and casing* and goniometer, expressed by Pearson*s correlation coefficient Precision ; Reliability: ICC for intra and inter-rater reliability and Standard Error of Measurement/ Smallest Detectable Change / Limits of agreement ( Bland & Altman plot) | — |
Secondary
| Measure | Time frame |
|---|---|
| Baseline parameters like age, sex, affected arm, and trauma mechanism will be collected. | — |
Countries
Netherlands
Outcome results
None listed