Electrical Vestibular Nerve Stimulation (VeNS) as a Treatment for Anxiety in Adolescents

This double blind randomized controlled trial will enroll up to 60 subjects and will be conducted at the BGS MCH Hospital. The study will be randomized for a 8-week period with a 1:1 active to sham device allocation. Each participant will complete 5 stimulation sessions per week under the supervision of a researcher at the clinic. Each session will be 30 minutes on the day of usage. The scheduled study events are to be undertaken at the following timepoints: * Baseline: Study Visit 1 (0-week timepoint for enrolment) * Study Visit 2 (2-week timepoint) * End of Study (4-week timepoint) * Post-intervention follow-up at 2 weeks (6-week timepoint) * Post-intervention follow-up at 6 weeks (10-week timepoint) * Post-intervention follow-up at 8 weeks (12-week timepoint)