Referral and consultation
Clarify the reason for referral, diagnosis, onset, relevant medical and dental history, functional priorities, and the patient’s goals.
Provider & clinic login
The clinical workflow
ISO Metrik connects clinical screening, structured resistance, repeatable exercise parameters, and clinic-to-home continuity in one facial neuromuscular rehabilitation workflow.
Six connected stages
Every stage keeps patient selection, safety, measurement, progression, and home-use decisions under qualified provider direction.
Clarify the reason for referral, diagnosis, onset, relevant medical and dental history, functional priorities, and the patient’s goals.
Review healing status, pain, temporomandibular-joint concerns, dentition, oral tissue integrity, cognition, precautions, and the need for medical or dental clearance.
Document facial symmetry, selective movement, oral-motor control, lip closure, endurance, coordination, functional limitations, and patient-reported concerns.
Select and assemble appropriate components, establish a comfortable fit, teach insertion and removal, and verify sanitation and storage procedures.
Choose the resistance mode, position, repetitions, hold time, rest interval, cueing strategy, and stopping criteria for the individual plan.
Repeat comparable measures, review tolerance and adherence, update goals, and advance one or more parameters only when clinically appropriate.
What the provider evaluates
The relevant domains depend on the patient’s diagnosis, scope of practice, and functional priorities.
Observe movement initiation, excursion, selectivity, compensations, symmetry, and control across relevant expressions.
Assess lip closure, oral seal, containment, coordination, and motor performance for appropriate speech or swallowing goals.
Record the ability to generate, maintain, and repeat a controlled effort without loss of form or excessive fatigue.
Connect findings to speaking, drinking, eating, expression, social confidence, and other patient-prioritized activities.
Track pain, pressure, skin or oral irritation, jaw symptoms, fatigue, dizziness, and any other adverse response.
Confirm that the patient can reproduce the assigned setup, dosage, cleaning process, and stopping rules.
Resistance modes
The platform supports a structured progression from activation to functional movement and controlled pacing.
The patient activates the selected muscles against resistance while holding a stable position.
The patient moves through a selected range while working against a consistent external resistance.
The patient performs a provider-paced movement with emphasis on consistent speed and controlled effort.
Inside a treatment session
A typical supervised session begins with a symptom and tissue check, confirmation of device fit, and a brief review of the prior response. The provider then selects the target movement and establishes the day’s parameters.
The patient practices under direct observation so the provider can cue alignment, limit substitutions, monitor fatigue, and stop the activity when movement quality or tolerance changes.
Progression decisions
A patient does not progress simply because a calendar interval has passed. The provider compares performance, function, technique, and recovery response.
Prioritize controlled, selective movement before increasing resistance, repetitions, range, or session duration.
When practical, alter one main parameter at a time so the clinical response can be interpreted more clearly.
Allow adequate rest, review delayed symptoms, and reduce or pause the program when tolerance or movement quality declines.
Patient selection and safety
Do not introduce active resistance during flaccid paralysis unless an appropriately qualified clinician determines that it is safe and indicated.
Confirm diagnosis, healing status, precautions, and required medical clearance after surgery, trauma, stroke, or other neurological events.
Review dentition, oral appliances, recent dental work, jaw pain, instability, and temporomandibular-joint symptoms.
Do not use the device over open lesions, active infection, uncontrolled bleeding, or tissue that cannot tolerate contact.
Confirm that the patient can understand the setup, recognize stopping criteria, and complete cleaning and storage safely.
New neurological symptoms, breathing or swallowing emergencies, severe pain, or acute medical change require appropriate urgent evaluation—not device use.
Start the right conversation
Discuss clinical implementation, training, research, provider onboarding, or clinic registration.