At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Feasibility Assessment of A Novel Wearable Skin Sensor for Post-Operative Monitoring Following Anterior Cervical Discectomy and Fusion (ACDF)
In Brief
A clinical study evaluating Anterior Cervical Discectomy & Fusion and Application of ADAM mechanoacoustic skin sensor for Cervical Spine Fusion. Completed, enrolled 11 participants across 1 site.
Detailed Summary
The purpose of this study is to assess the function and reliability of a noninvasive, skin-like electronic sensor. The investigators hypothesize that this skin sensor will address an unmet need to wirelessly and noninvasively monitor and characterize the recovery process in post-operative patients who have undergone anterior cervical discectomy and fusion (ACDF). Specifically, the investigators will validate the use of the sensor in this patient population through monitoring of key physiological signals in the recovery process, including heart rate, respiratory rate, swallow count, talking time, energy expenditure, neck specific motion, and body orientation.
Study Details
Timeline
Interventions
Participants are undergoing previously scheduled anterior cervical discectomy \& fusion for single level or multiple level cervical disease
Applying the ADAM sensor to the suprasternal notch following surgery to allow for collection of the anatomical data