Effectiveness Ankle-7 Orthosis VS HAFO Orthosis on Gait in Diplegic CPChildren

The project is divided into the following phases: T0 - at the beginning of the study children included will be subject to the following procedures and assessments: 1. demographic and anthropometric data collection; 2. randomization by concealed allocation to one of the following two groups: * AFO - Ankle\_7 group * Ankle-7 - AFO group Both, AFO and ankle-7, will be tailored to the patient The two groups are distinguished by the order of the assignment of the two orthoses, respectively defined as the first assignment orthosis (O\_1) and second assignment orthosis (O\_2). The first group will use the orthoses AFO as a first assignment and then the orthoses Ankle\_7, while the second group will use the two orthoses according to the reverse order. The two will be used with the same orthotic footwear, with the exception of the cases where it will be necessary to change it due to accretion. 3. collection of the measures necessary for making the two orthotic devices at OttoBock of Reggio Emilia 4. training in the use of the orthoses according to a standardized protocol; 5. try on the patient's in-process first assignment orthoses (O\_1) and subsequent delivery of them (see Annex A); Subsequently, the patient will use O\_1 for a period of 4-6 weeks. T1 - patients will receive the following procedures and assessments: 1. try on the patient's in-process second assignment orthoses (O\_2) 2. instrumental gait analysis and video recording of the walking while using O\_1 (covered by elastic gaiters); 3. withdrawal of O\_1 4. delivery of O\_2 to the patient Subsequently, the patient will use O\_2 for a period of 4-6 weeks. T2 - patients will undergo the following procedures and evaluations: 1. instrumental gait analysis and video recording of the walking while using O\_2 (covered by elastic gaiters); 2. return of O\_1 to the patient; 3. Delivery of the diaries and directions for completing and mailing back them at the end of the follow-up period; T3 - three months follow-up to detect the preference of use of AFO or Ankle-7 (by the child/parent)