Flexible Flatfoot. Flat foot [pes planus] (acquired)
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 18-40 year old people Navicular drop test >= 10 mm Foot posture index score between +6 to +12 Positive toe raise test BMI between 20-25
Exclusion criteria
Exclusion criteria: Ankle injury in the last six months History of foot surgery Foot injury due to systemic, inflammatory and infectious diseases Foot deformities include hallux valgus, hammer toe, claw toe Pregnancy Ankle pain during the study Static standing and walking problems Kinesio tape sensitivity Refuse to participate in the study or cancel continuing treatment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Navicular drop test score. Timepoint: At the beginning of the study and after 30 minutes of intervention. Method of measurement: Index card and ruler.;Foot posture index score. Timepoint: At the beginning of the study and after 30 minutes of intervention. Method of measurement: Observation.;Y balance test score. Timepoint: At the beginning of the study and after 30 minutes of intervention. Method of measurement: Meter.;Timed up and go test score. Timepoint: At the beginning of the study and after 30 minutes of intervention. Method of measurement: stopwatch.;Mean length/width of gait line. Timepoint: At the beginning of the study and after 30 minutes of intervention. Method of measurement: Moticon insole and software.;Mean and maximum total force of stance phase. Timepoint: At the beginning of the study and after 30 minutes of intervention. Method of measurement: Moticon insole and software.;Mean double support time. Timepoint: At the beginning of the study and after 30 minutes of intervention. Method of measurement: Moticon insole and software.;Mean stance and swing duration. Timepoint: At the beginning of the study and after 30 minutes of intervention. Method of measurement: Moticon insole and software.;Center of pressure amplitude in mediolateral direction. Timepoint: At the beginning of the study and after 30 minutes of intervention. Method of measurement: Moticon insole and software.;Center of pressure amplitude in anteroposterior direction. Timepoint: At the beginning of the study and after 30 minutes of intervention. Method of measurement: Moticon insole and software.;Center of pressure standard deviation in mediolateral direction. Timepoint: At the beginning of the study and after 30 minutes of intervention. Method of measurement: Moticon insole and software.;Center of pressure standard deviation in anteroposterior direction. Timepoint: At the beginning of the study and after 30 minutes of intervention. Method of measurement: Moticon insole and software.;Mean | — |
Countries
Iran (Islamic Republic of)
Contacts
Tehran University of Medical Sciences