Pilot Study of Intervention to Reduce Sunburns in Melanoma Survivors

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Clinical Phase

NA

Study Classification

INTERVENTIONAL

Study Start Date

2020-02-29

Study Completion Date

2021-05-31

Brief Summary

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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.

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Detailed Description

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Conditions

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Melanoma (Skin)

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Intervention

Microsoft Band 2 application with UV messaging activated

Group Type EXPERIMENTAL

Microsoft Band 2 + UV messaging

Intervention Type DEVICE

wearable device (wrist) and associated mobile application; UV sensor and messaging activated

Control

Microsoft Band 2 application (UV messaging not active)

Group Type ACTIVE_COMPARATOR

Microsoft Band 2

Intervention Type DEVICE

wearable device (wrist) and associated mobile application; UV messaging not activated

Interventions

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Microsoft Band 2 + UV messaging

wearable device (wrist) and associated mobile application; UV sensor and messaging activated

Intervention Type DEVICE

Microsoft Band 2

wearable device (wrist) and associated mobile application; UV messaging not activated

Intervention Type DEVICE

Eligibility Criteria

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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