Chronic Ankle Instability. Sprain of ankle
Conditions
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: Age range of 18-40 years Both genders Amateur athletes (volleyball player, basketball player, or football player) engaging in moderate to vigorous physical activity (at least 3 times per week, each session lasting more than 30 minutes History of unilateral ankle sprain, at least 12 months prior to study entry (no more than 3 months since the last sprain at the time of study entry) Experience of recurrent episodes of ankle giving way or feelings of instability and having symptoms such as weakness, and decreased performance over the past year Scoring 24 or lower on the Cumberland Ankle Instability Tool
Exclusion criteria
Exclusion criteria: history of surgery or fractures in the ankle or lower extremity based on the patient's self-report No history of training with video games
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time during anticipatory postural adjustment. Timepoint: Before starting the intervention and 48 h after the last session. Method of measurement: Force Plate device(BertecCorporation,Columbus, OH, USA).;Time to new stability point. Timepoint: Before starting the intervention and 48 h after the last session. Method of measurement: Force Plate device(BertecCorporation,Columbus, OH, USA).;Anterior-Posterior/Medial-Lateral and Resultant center of pressure displacement during double-leg stance phase. Timepoint: Before starting the intervention and 48 h after the last session. Method of measurement: Force Plate device(BertecCorporation,Columbus, OH, USA).;Anterior-Posterior/Medial-Lateral and Resultant center of pressure velocity during double-leg stance phase. Timepoint: Before starting the intervention and 48 h after the last session. Method of measurement: Force Plate device(BertecCorporation,Columbus, OH, USA).;Anterior-Posterior/Medial-Lateral and Resultant center of pressure displacement during intermediate phase. Timepoint: Before starting the intervention and 48 h after the last session. Method of measurement: Force Plate device(BertecCorporation,Columbus, OH, USA).;Anterior-Posterior/Medial-Lateral and Resultant center of pressure velocity during intermediate phase. Timepoint: Before starting the intervention and 48 h after the last session. Method of measurement: Force Plate device(BertecCorporation,Columbus, OH, USA).;Anterior-Posterior/Medial-Lateral and Resultant center of pressure displacement during the first 3 seconds after time to new stability point phase. Timepoint: Before starting the intervention and 48 h after the last session. Method of measurement: Force Plate device(BertecCorporation,Columbus, OH, USA).;Anterior-Posterior/Medial-Lateral and Resultant center of pressure velocity during the first 3 seconds after time to new stability point. Timepoint: Before starting the intervention and 48 h after the last session. Method of measurement: Force Plat | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSadaf Sepasgozar Sarkhosh
Tehran University of Medical Sciences
Outcome results
None listed