Infrared Photomodulation Therapy for Seasonal Affective Disorder
Not Applicable
Completed
- Conditions
- Seasonal Affective Disorder
- Interventions
- Device: Joovv Mini
- Registration Number
- NCT04251000
- Lead Sponsor
- ProofPilot
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 60
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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Joovv Pilot Experimenta Arm Joovv Mini Individuals will receive 90 day access to the Joovv infrared mini light device.
- Primary Outcome Measures
Name Time Method Change in Sleep Duration and Sleep Quality as measured by consumer connected health device Baseline to 90 day Measures of sleep and sleep quality as by a Withings or Oura Ring connected health device
Change in activity levels as measured by consumer connected health devices Baseline to 90 day Measures of activity levels as by WIthings our Oura connected health devices
change self report mood as assessed by Warwick Edinburgh sleep scale Baseline to 90 day non clinical measures of mood controlled for environmental temperature and daylight
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
ProofPilot (Virtual Study: https://proofpilot.com)
🇺🇸New York, New York, United States