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Neurology · Ataxia

What Is the SARA Score for Ataxia Progression?

At a Glance

The SARA (Scale for the Assessment and Rating of Ataxia) score is a clinical tool neurologists use to measure ataxia severity on a scale from 0 to 40. Tracking this score helps objectively monitor disease progression, predict physical therapy needs, and determine clinical trial eligibility.

The Scale for the Assessment and Rating of Ataxia (SARA) is a standardized, 5-to-10-minute clinical test neurologists use to measure the severity of ataxia symptoms [1]. When your neurologist gives you a SARA score, they are assigning a total number from 0 to 40 based on your physical coordination, where 0 means no ataxia and 40 represents the most severe ataxia [2][3]. This score provides an objective way to see exactly how your symptoms are changing over time [4].

The Eight Tasks of the SARA Assessment

During your appointment, the neurologist will ask you to perform a series of specific physical tests. The SARA assessment consists of exactly eight items, each testing a different aspect of motor coordination [3][1]:

  • Gait: You will be asked to walk a short distance. The doctor watches for unsteadiness, how wide your steps are, and whether you need support.
  • Stance: You will be asked to stand with your feet together, and sometimes with one foot in front of the other, to test your standing balance.
  • Sitting: You will sit on an exam bed without back support and with your feet dangling to check your core balance.
  • Speech Disturbance: The doctor will listen to you talk, paying attention to dysarthria (slurred or uneven speech caused by muscle coordination issues).
  • Finger-Chase Test: The doctor will move their finger around, and you will be asked to follow it with your own finger.
  • Nose-Finger Test: You will touch your own nose and then reach out to touch the doctor’s finger, back and forth.
  • Fast Alternating Hand Movements: You will quickly flip your hands palm-up and palm-down on your lap to test speed and coordination.
  • Heel-Shin Slide Test: While lying down or seated, you will slide the heel of one foot down the shin of your opposite leg to check lower body coordination.

Your performance on each task is graded and then added together to create your total SARA score. Because some skills impact your daily life more than others, the tasks carry different maximum point values—for example, gait is scored out of 8 points, while sitting balance is scored out of 4 [2][3].

Why Tracking Your SARA Score Matters

In conditions like autosomal dominant cerebellar ataxia (often referred to as spinocerebellar ataxia or SCA), symptoms change slowly. It can be difficult for both you and your doctor to notice tiny differences from month to month. Tracking your SARA score annually helps your neurologist measure disease progression objectively rather than relying on memory or guesswork [4][5].

A higher score generally corresponds to a greater impact on your daily life, and tracking it can help predict your future needs for physical therapy, walking aids, or home modifications [5][6].

It is completely normal to feel emotionally exhausted or anxious when taking this test. Watching a doctor objectively quantify changes in your body can be difficult. It is also important to remember that progression is not always constant [7]. You might see small fluctuations in your score—going up slightly one visit and stabilizing the next. Factors like fatigue, stress, a poor night’s sleep, or fighting off a mild illness can make your ataxia temporarily worse on the day of the test [8].

While progression rates vary widely depending on the exact subtype of ataxia and the age your symptoms began, a typical progression for many genetic ataxias might be an increase of 1 to 2 points per year [4]. Therefore, a slight bump in your score does not necessarily mean a rapid decline in your day-to-day abilities.

Finally, because SARA is considered a highly reliable reference tool in research, knowing your score can help determine if you are eligible for certain clinical trials [3][4][1]. Experimental treatments rely on this scale to prove whether a new therapy is effective at slowing the disease.

Common questions in this guide

What does a SARA score of 0 to 40 mean?
The SARA score ranges from 0 to 40. A score of 0 indicates no ataxia symptoms, while a score of 40 represents the most severe level of ataxia. A higher number generally means your coordination issues have a greater impact on your daily life.
What physical tests are included in the SARA assessment?
The assessment includes exactly eight tasks that test different aspects of your motor coordination. You will be asked to walk, stand, sit without support, speak, and perform specific hand and leg movements like following a doctor's finger.
How fast does the SARA score typically increase?
While progression rates vary based on your specific subtype of ataxia and age of onset, a typical progression for many genetic ataxias is an increase of 1 to 2 points per year. A slight increase does not automatically mean a rapid decline in your abilities.
Why is my doctor tracking my SARA score?
Tracking your score provides an objective measurement of how your disease is progressing over time, which is more reliable than memory. It helps your neurologist anticipate when you might need physical therapy or walking aids, and it can determine your eligibility for clinical trials.
Can lack of sleep or stress affect my ataxia score?
Yes. Temporary factors like fatigue, severe stress, a poor night's sleep, or fighting off a mild illness can make your ataxia symptoms temporarily worse. This can lead to a slight increase in your SARA score on the day of your appointment that isn't related to actual disease progression.

Questions to Ask Your Doctor

Curated prompts to bring to your next appointment.

  1. 1.What was my total SARA score today, and how does it compare to my baseline from previous visits?
  2. 2.Which specific tasks in the SARA assessment are driving the highest points in my score, and are there physical therapy exercises to target those areas?
  3. 3.Does my current SARA score indicate that I should be considering walking aids or home modifications to reduce my fall risk?
  4. 4.Am I in a score range that would qualify me for any active clinical trials for spinocerebellar ataxia?
  5. 5.If my score increased today, how much of that do you think could be related to my current fatigue levels versus actual disease progression?

Questions For You

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References

References (8)
  1. 1

    Ataxia Rating Scales: Content Analysis by Linking to the International Classification of Functioning, Disability and Health.

    Etoom M, Jahan AM, Alghwiri A, et al.

    Healthcare (Basel, Switzerland) 2022; (10(12)) doi:10.3390/healthcare10122459.

    PMID: 36553983
  2. 2

    Item performance of the scale for the assessment and rating of ataxia in rare and ultra-rare genetic ataxias.

    Hamdan A, Hooker AC, Chen X, et al.

    CPT: pharmacometrics & systems pharmacology 2024; (13(8)):1327-1340 doi:10.1002/psp4.13162.

    PMID: 38769902
  3. 3

    Temporal Dynamics of the Scale for the Assessment and Rating of Ataxia in Spinocerebellar Ataxias.

    Moulaire P, Poulet PE, Petit E, et al.

    Movement disorders : official journal of the Movement Disorder Society 2023; (38(1)):35-44 doi:10.1002/mds.29255.

    PMID: 36273394
  4. 4

    Progression characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS): a 2 year cohort study.

    Reetz K, Dogan I, Hilgers RD, et al.

    The Lancet. Neurology 2016; (15(13)):1346-1354 doi:10.1016/S1474-4422(16)30287-3.

    PMID: 27839651
  5. 5

    Predictive Validity of the Scale for the Assessment and Rating of Ataxia for Medium-Term Functional Status in Acute Ataxic Stroke.

    Yamauchi K, Kumagae K, Goto K, et al.

    Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2021; (30(4)):105631 doi:10.1016/j.jstrokecerebrovasdis.2021.105631.

    PMID: 33508726
  6. 6

    Neurologic outcomes in Friedreich ataxia: Study of a single-site cohort.

    Pandolfo M

    Neurology. Genetics 2020; (6(3)):e415 doi:10.1212/NXG.0000000000000415.

    PMID: 32337342
  7. 7

    The progression rate of spinocerebellar ataxia type 2 changes with stage of disease.

    Monte TL, Reckziegel EDR, Augustin MC, et al.

    Orphanet journal of rare diseases 2018; (13(1)):20 doi:10.1186/s13023-017-0725-y.

    PMID: 29370806
  8. 8

    Exploring the clinical meaningfulness of the Scale for the Assessment and Rating of Ataxia: A comparison of patient and physician perspectives at the item level.

    Maas RPPWM, van de Warrenburg BPC

    Parkinsonism & related disorders 2021; (91()):37-41 doi:10.1016/j.parkreldis.2021.08.014.

    PMID: 34479057

This page provides educational information about the SARA score for ataxia. It is not a substitute for professional medical advice, diagnosis, or a formal neurological assessment.

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