Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Fibromyalgia
  • FMS
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Double (Participant, Outcomes Assessor)Masking Description: The outcome assessors and participants will be blinded to condition. The PI and lab manager will remain unblinded, and perform the fidelity and side effects assessments. Participants are asked and reminded throughout the study to only speak about their light treatment with either the PI or lab manager.Primary Purpose: Supportive Care

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

Not Provided

Not Provided

Tracking Information

NCT #
NCT03794908
Collaborators
National Institute of Nursing Research (NINR)
Investigators
Principal Investigator: Helen Burgess University of Michigan