Actively Recruiting
IBD-Sleep: A Pilot Study Looking at Changes in Sleep Timing and IBD Symptoms
Led by University of Michigan · Updated on 2026-04-27
68
Participants Needed
1
Research Sites
177 weeks
Total Duration
On this page
Sponsors
U
University of Michigan
Lead Sponsor
N
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research study is testing whether changes in sleep timing and morning light treatment may have an impact on symptoms related to inflammatory bowel disease.
CONDITIONS
Official Title
IBD-Sleep: A Pilot Study Looking at Changes in Sleep Timing and IBD Symptoms
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Biopsy-proven inflammatory bowel disease
- Active inflammatory bowel disease symptoms
- Impaired quality of life related to inflammatory bowel disease
- Age 18 years or older
- Fluent in English
- Physically able to travel for study visits
You will not qualify if you...
- Having or planning ileostomy, colostomy, ileoanal pouch, or ileorectal anastomoses surgery, or having short bowel syndrome
- Presence of other significant chronic diseases
- Retinal problems, history of eye surgery, or taking photosensitizing medications
- Recent history of light treatment
- Lifetime psychotic or bipolar disorder
- Acute suicidal thoughts
- Substance use disorder in the past 3 months or cannabis use more than once per week
- High risk for or diagnosis of obstructive sleep apnea or narcolepsy
- Severe hearing problems, intellectual disability, or serious cognitive impairment
- Pregnant, trying to become pregnant, or breastfeeding
- Night shift work or travel outside the eastern time zone in the past month
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Michigan
Ann Arbor, Michigan, United States, 48105
Actively Recruiting
Research Team
H
Helen Burgess
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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