Infrared Photomodulation Therapy for Seasonal Affective Disorder

ProofPilot60 enrolled

Overview

During winter months in northern latitudes use of Joovv device on self-reported non-clinical mental health (aka mood), sleep and energy levels. Participants will also submit Withings and Oura activity and sleep data.

Study Type

INTERVENTIONAL

Allocation

Purpose

PREVENTION

Masking

NONE

Enrollment

Conditions

Seasonal Affective Disorder

Interventions

Joovv MiniDEVICE

the smallest photomodulation device in the Joovv infrared light product line.

Eligibility

Sex: ALLMin age: 18 YearsMax age: 100 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * history of mental health issues including clinical depression * US based * reasonably active individuals (self report run/gym 3x per week or more) Exclusion Criteria: * average daily high temperature in zipcode above 60 degrees through end of March

Locations (1)

ProofPilot (Virtual Study: https://proofpilot.com)

New York, New York, United States

Outcomes

Primary Outcomes

change self report mood as assessed by Warwick Edinburgh sleep scale

non clinical measures of mood controlled for environmental temperature and daylight

Time frame: Baseline to 90 day

Change in Sleep Duration and Sleep Quality as measured by consumer connected health device

Measures of sleep and sleep quality as by a Withings or Oura Ring connected health device

Time frame: Baseline to 90 day

Change in activity levels as measured by consumer connected health devices

Measures of activity levels as by WIthings our Oura connected health devices

Time frame: Baseline to 90 day

Data from ClinicalTrials.gov

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