A Usability Study of a Multi-channel ECG Monitoring Device
Wearlinq · with ABio Clinical Research Partners · NCT07388355
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 500
- US sites recruiting
- 1
- Study start
- July 6, 2026
- Record last updated
- July 21, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
This study it to evaluate the usability of the WearLinq eWave patch in a general adult population.
Being studied: eWave Patch
Conditions: Healthy Adult Participants; Heart Disease; Arrythmia; Cardiac
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Adult >18 years old and able to consent
- Capable of using a smartphone app
- Willing to shave patch area if needed
Exclusion Criteria
- Planning to undergo an MRI during the study period
- Known allergic reaction to adhesives or hydrogels or with family history of adhesive skin allergies, or any other dermatological conditional that could confound placement or results
- Presence of pacemaker, ICD or other implanted electronic devices
- Open wounds, lesions or infected or inflamed areas of skin at the placement site (left-center of chest/sternum)
- Pregnant or intending to become pregnant during the course of the study
Recruiting US locations
ABio Clinical Research Partners
New London, NC 28127
Site contact: Andrea Brown, MS · 408-881-2611 · wearlinqstudy@abioclinical.com
Study contacts (from the official record)
- Andrea Brown, MS · 408-881-2611 · abrown@abioclinical.com
- Chris Daniel · chris@wearlinq.com
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