No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
500 (estimated)
Sponsor
Wearlinq · Industry
Who this trial is looking for
This trial is looking for adults over 18 to test the WearLinq eWave patch. Participants will help evaluate how easy it is to use this heart monitoring device.
Are You a Good Fit for This Trial?
You may be able to join if
I am over 18 years old
I can use a smartphone app
I am willing to shave the patch area if needed
You may not be able to join if
I plan to have an MRI during the study
I am allergic to adhesives or hydrogels
I have a pacemaker or other implanted electronic device
I have open wounds or infections at the patch site
I am pregnant or planning to become pregnant during the study
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
This study it to evaluate the usability of the WearLinq eWave patch in a general adult population.
Trial Locations
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City
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Status
Eligibility 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 adhesiv…
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
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