VigNet Inc. — Department of Health and Human Services SBIR Phase II: NCI

VigNet Inc. — SBIR Phase II award from Department of Health and Human Services.

Amount
$1,499,971
Agency
Department of Health and Human Services · National Institutes of Health
Program / Phase
SBIR · Phase II
Topic
NCI
NAICS
Place of performance
VA
Period

Description

Despite recent advances in immunotherapy and molecularly targeted therapies for advanced melanoma early detection remains the most effective means of preventing death from melanoma Currently physicians have no uniform way to efficiently and effectively teach the million people at risk to develop melanoma how to check their skin for melanoma Melanoma patients are not provided with communication materials to inform their first degree relatives of their risk of developing melanoma and how to engage their relatives in managing their risk by performing skin self examination to improve early detection of melanoma and their survival from this deadly disease The weakness in the current health care system result in undue anxiety among relatives of melanoma patients unnecessary visits to the dermatologist with unnecessary skin biopsies and increased cost to the health care system Through a RCT we will validate the use of Eviderma that extends the proven physician to physician consultation of the Vignet Mobile Telederm system to provide melanoma patients and their first degree relatives education about their risk of developing melanoma and the importance of early detection teach the skills to perform SSE provide diaries for home use and access to dermatologists The melanoma patient and relative will download the Eviderma and self report their adherence to their care plan by learning how to perform SSE report their SSE results and send the dermatologist a picture of a pigmented lesion mole and the dermatologist will recommend next steps We hypothesize that melanoma patients and first degree relatives who use Eviderma will a improve their awareness of being at risk of developing melanoma importance of early detection and SSE performance b learn to engage dermatologists effectively and efficiently for skin examination of concerning lesions and c disseminate it to friends and relatives We will conduct a randomized clinical trial in order to develop and rigorously test Eviderma In addition we will assess the direct costs such as physician visits for screening biopsy of concerning moles and the pathologic interpretation as well as the projected cost of care of advanced melanoma when early detection failed Indirect costs for the patient including travel time lost from work and family will also be assessed The impact of a successful trial should be to fill the current gap in the care of melanoma patients and their first degree relatives reduce health care costs improve patient adherence to SSE performance detect melanoma in the curable stage and reduce mortality