Pilot Study of Intervention to Reduce Sunburns in Melanoma Survivors

Melanoma (Skin) Clinical Trial

Official title:

Pilot Study of Intervention to Reduce Sunburns in Melanoma Survivors

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT03518229
• Other study ID #: STUDY00002107
• Status: Withdrawn
• Phase: N/A
• Start date: February 2020
• Est. completion date: May 2021

Study information

• Verified date: April 2019
• Source: University of Minnesota - Clinical and Translational Science Institute
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This project will pilot test whether a wearable device that tracks sun exposure and provides alerts regarding sun exposure and protection behaviors will reduce sunburns in melanoma survivors. The use of wearable technology devices has grown quickly over the last decade and studies using these devices to promote physical activity and weight loss have been promising. The investigators will pilot test the technology device versus a similar control device in 80 melanoma survivors and compare sunburns between the two groups after the three month intervention.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: May 2021
• Est. primary completion date: September 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• 18-75 years old

• Diagnosed with stage I-III cutaneous invasive melanoma between 2009 and 2017 and treated at the University of Minnesota

• Able to read/write in English

• Own a smartphone

• Able to provide voluntary informed consent

Exclusion Criteria:

-Patients currently undergoing adjuvant therapy.

Related Conditions & MeSH terms

• Melanoma
• Melanoma (Skin)
• Sunburn

Intervention

Device:
• Microsoft Band 2 + UV messaging
wearable device (wrist) and associated mobile application; UV sensor and messaging activated
• Microsoft Band 2
wearable device (wrist) and associated mobile application; UV messaging not activated

Locations

Country	Name	City	State
n/a

Sponsors (2)

Lead Sponsor	Collaborator
University of Minnesota - Clinical and Translational Science Institute	Melanoma Research Alliance

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Sunburn	Self-report of a sunburn during study period	3 months