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The objective of this study is to evaluate an experience of post-operative monitoring using the Nanowear wearable multiple sensor vest in plastic surgery
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Observational Study: No intervention | Device | Observational Study: No intervention |
| Measure | Description | Time Frame |
|---|---|---|
| Subject assessment of comfort and compliance | 1. Subject assessment of comfort and compliance will be filled out by subjects using a 6-points Usability Survey, as follows:
| 7 days |
| Measure | Description | Time Frame |
|---|---|---|
| Investigator assessment of device usability and satisfaction | 2. Investigator assessment of device usability will be filled out by PI using a 4-points Likert scale, as follows: 3 = Extremely useful in post op care; 2 = Useful in post op care; 1 = Somewhat useful in post op care; 0 = Useless in post op care. 3. Investigator assessment of satisfaction will be filled out by PI using a 5-points Likert scale, as follows: +2 = Very satisfied; +1 = Satisfied; 0 = Indifferent; -1 = Disappointed; -2 = Extremely disappointed. |
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Inclusion Criteria:
Exclusion Criteria:
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Male or female over the age of 18 years, healthy adults scheduled to undergo BodyTite and/or FaceTite procedures.
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Zucker School of Medicine, Hofstra University | New York | New York | 10019 | United States |
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| through study completion, an average of 1 year |