Testing light therapy and sleep changes for fibromyalgia symptoms
At Home Morning Bright Light Treatment for Chronic Nociplastic Pain
This study is testing if using a special light in the morning and changing sleep habits can help people with fibromyalgia feel better.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 390 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Michigan Academic / other |
| Locations | 1 site (Ann Arbor, Michigan) |
| Trial ID | NCT06567886 on ClinicalTrials.gov |
What this trial studies
This study investigates the effects of sleep timing stabilization and morning light therapy on symptoms of fibromyalgia. Participants will use a consumer health light therapy device called Re-Timer to assess its impact on their condition. The study will be conducted remotely, allowing participants to engage via video conferencing. The goal is to determine if these interventions can improve the quality of life for individuals suffering from fibromyalgia.
Who should consider this trial
Good fit: Ideal candidates are individuals diagnosed with fibromyalgia who have access to video conferencing technology.
Not a fit: Patients with significant chronic diseases or severe cognitive impairments may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a non-invasive treatment option to alleviate fibromyalgia symptoms.
How similar studies have performed: Other studies have shown promising results with light therapy for various conditions, suggesting potential for success in this novel application.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Meets 2016 revised diagnostic criteria for fibromyalgia (FM) 2. Has access to video conferencing (including web cameras and audio) and a private space for the remote study visits. Exclusion Criteria: 1. Significant chronic disease 2. Severe hearing or memory problems 3. Pending medical leave applications at workplace 4. Current pregnancy, breastfeeding, or actively trying to get pregnant 5. Night work or travel outside the eastern time zone within 1 month of the study 6. Other research participation 7. Frequent number of special events during study period (weddings, concerts, exams, etc).
Where this trial is running
Ann Arbor, Michigan
- University of Michigan — Ann Arbor, Michigan, United States (Recruiting)
Study contacts
- Principal investigator: Afton Hassett — University of Michigan
- Study coordinator: Helen Burgess
- Email: bhelen@umich.edu
- Phone: 734-615-8303
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.