Cala Health Reports: New Data Demonstrate How Cala Trio™ Enables a More Frequent Assessment of Hand Tremor Compared with In-Person Assessments in Patients with Essential Tremor and Supports Feasibility of Telemedicine Approaches for Essential Tremor Management

April 15, 2021

Cala Health, Inc. (developer of wearable therapies for chronic disease) today announces new data confirming that in-person assessments may not fully capture at-home hand tremor fluctuations for patients with essential tremor (ET).

Additional new data demonstrate that an evaluation of hand tremor can be performed via telemedicine appointment to prescribe Cala Trio™. Both abstracts indicate that telemedicine and remote patient monitoring can improve care access and reduce patient treatment burden. The data are being presented in two poster presentations at AAN 2021, which is being held virtually April 17-22.

“COVID-19 has underscored the importance of remote health delivery and assessment strategies in providing effective care to patients with chronic diseases, especially those with movement disorders,” said Kate Rosenbluth, Ph.D., Founder and Chief Scientific Officer of Cala Health. “The new data presented at AAN demonstrate that how the Cala Trio therapy can also be used for home-based tracking of action tremor severity and response to therapy. This can provide insights for patients, physicians, and caregivers.”

Ruta Deshpande, Clinical Research Engineer at Cala Health, will present data from an abstract titled “Remote assessment of action tremors during COVID-19: A pooled meta-analysis of transcutaneous afferent patterned stimulation in Parkinson’s Disease and Essential Tremor” (Abstract #1981) in a poster session.

The poster characterizes the strengths of a single day (e.g., in-clinic) vs. repeated (e.g., multi-day, at home) measurements of tremor for assessment of a patient’s tremor burden and response to tremor therapies. This analysis included in-person clinical assessments of tremor and repeated at-home motion sensor assessments. Clinical ratings were correlated to simultaneously measured sensor assessments, suggesting motion sensors can provide a valid assessment of tremor outside the clinic.

However, because tremor has considerable day-to-day variability, neither clinical assessments nor motion sensor assessments at a single time point are sufficient to capture a patient’s daily tremor burden. Motion sensors enable repeated assessments, and these multi-day assessments are shown to have higher reliability in capturing tremor burden. Moreover, repeated measurements allow for a more robust characterization of any intervention response, including response to TAPS.

“These findings demonstrate that Cala Trio, through the power of bioelectronic medicine and repeated, at-home measurements provides consistent measures of tracking tremor severity and response to therapy in patients with movement disorders,” said Ms. Deshpande.

Deshpande added, “The data also suggest that periodic, in-person assessments might not always capture daily at-home improvements and demonstrate how wearable sensors can be incorporated into remote clinical studies via telemedicine for patients with movement disorders. The results also suggest that repeated Cala Trio assessments of therapeutic response which are correlated to clinical gold-standard assessments can capture tremor burden, response to therapy and patient self-assessments.”

Salima Brillman, MD, a neurologist at and founder of the Parkinson’s Disease and Movement Disorder Center of Silicon Valley, authored the abstract “Essential tremor patients managed through in-person and telemedicine have similar experiences with prescribed non-invasive neuromodulation therapy” (Abstract #1542) in the poster session.

The abstract reports real-world evidence (RWE) analyzed to assess the effect of prescription setting on patient experience with Cala Trio. In this study, patient experience was evaluated by time from prescription to shipment to the patient; at-home therapy usage and therapy efficacy were quantified using median improvement in device-measured tremor power.

The RWE analyzed a total of 265 patients, 13 of whom were from a single telemedicine prescriber; the comparative cohorts included patients using the device for at least 30 days and with at least 10 sessions of valid accelerometer data available for analysis. Results show that both patient cohorts had similar device use patterns, with patients typically completing 1-2 sessions/day on 2.6 days/week (median; range 0-7 days/week). Objective motion data from 12,731 sessions (613 from telemedicine cohort) showed 88% of all patients (77% telemedicine cohort) had ≥a 2-fold improvement in tremor power during their most severe sessions when tremor relief might be most needed.

The study also found that 53% of all patients (31% telemedicine patients) had ≥2-fold improvement in tremor power aggregated over all sessions.

“In this study, no differences were observed in the patient experience regardless of their Cala Trio being prescribed in-person or via telemedicine. This suggests that patient management via telemedicine is a feasible way to evaluate and treat patients with ET without sacrificing health outcomes,” said Dr. Brillman. “While telemedicine has been critical to ensuring that patients can receive care during the COVID-19 pandemic, its use in more routine care may help to increase access and reduce patients’ treatment burdens. These findings are especially important in patients with movement disorders who frequently require assistance from caregivers to attend in-person visits with a physician.”

The results from these abstracts suggest that the use of Cala Trio in telemedicine settings may help patients with movement disorders improve the management of their action-based tremors while reducing their treatment burden through virtual interactions with their healthcare professionals. Cala Trio, a non-invasive personalized solution that reduces hand tremors, is currently FDA-cleared for essential tremor. In October 2020, the FDA granted Breakthrough Device Designation to Cala Trio to treat action tremors in the hands of adults with PD, and the company initiated a clinical trial in this indication in November 2020.

Hot this week

Cartessa Aesthetics Partners with Classys to Bring EVERESSE to the U.S. Market

Classys, which is listed on the KOSDAQ, is one of South Korea's most distinguished aesthetic technology manufacturers, with devices distributed in 80+ markets globally. This partnership marks Classys's official entry into the American marketplace, with Cartessa Aesthetics as the exclusive distributor for EVERESSE, launched under the Volnewmer brand in current global markets.

Stryker Launches Next-Generation of SurgiCount+

Now integrated with Stryker's Triton technology, SurgiCount+ addresses two key challenges: retained surgical sponges and blood loss assessment. Integrating these previously separate digital solutions provides the added benefit of a more efficient, streamlined workflow for hospitals notes Stryker.

Nevro Receives CE Mark In Europe for It’s HFX iQ™ Spinal Cord Stimulation System

Nevro notes HFX iQ is the first and only SCS system with artificial intelligence (AI) technology that combines high-frequency (10 kHz) therapy built on landmark evidence that uses ongoing cloud data insights to deliver personalized pain relief

Recor Medical Reports: CMS Grants Distinct TPT Device Code and Category to Recor Medical for Ultrasound Renal Denervation

The approval of TPT offers incremental reimbursement payments for outpatient procedures performed with ultrasound renal denervation for Medicare fee-for-service beneficiaries. It becomes effective January 1, 2025, and is expected to remain effective for up to three years notes Recor Medical.

Jupiter Endovascular Reports | 1st U.S. Patient Treated with Jupiter Shape-shifting Thrombectomy Device

“Navigation challenges during endovascular procedures are often underappreciated and have led to under-adoption of life-saving procedures, such as pulmonary embolectomy. We have purpose-built our Endoportal Control technology to solve these issues and make important endovascular procedures accessible to more clinicians and their patients who can benefit from them,” said Carl J. St. Bernard, Jupiter Endovascular CEO. “This first case in the U.S. could not have gone better, and appears to validate the safety and performance we are seeing in our currently-enrolling European SPIRARE I study.”