NeuFit is proud to sponsor the Case Study Initiative, encouraging NeuFit practitioners to share insights and outcomes from their use of the Neubie in various therapeutic contexts. This initiative aims to gather valuable data on the benefits and challenges encountered in different practices, helping to improve and innovate our approaches.
Follow these steps to ensure your submission is complete and eligible:
Review the case study submission criteria below, then gain inspiration and insight by reviewing sample case studies from other practitioners. You may use these for reference when you are crafting your Case Studies.

Each patient must sign the Patient Release Forms to consent to having their diagnosis, treatment, and outcomes shared, and the practitioner must sign the Case Study release forms as well.

We value your participation and are excited to hear your impactful stories. By contributing to our Case Study Initiative, you play a crucial role in advancing our understanding and application of Neubie technology in rehabilitation and recovery.



We value your participation and are excited to hear your impactful stories!
*Because the Neubie Device is the maximum power allowed by law, there are certain regulations imposed by the United States FDA. Neubie may only be sold to an individual by or on the order of a licensed practitioner. Neubie may only be used commercially by a licensed practitioner or under the supervision of a licensed practitioner whose scope of practice covers the use of electrical modalities.