Circadian Amplification in Diabetic Retinopathy

Description

This study will test the effects of a 6-week comprehensive circadian optimization intervention Amplify-RHYTHM in patients with diabetic retinopathy. The outcomes of interest are objective and subjective sleep parameters, evening salivary cortisol and melatonin levels, and glucose parameters from continuous glucose monitoring

Conditions

Diabetic Retinopathy

Study Overview

Study Details

Study overview

This study will test the effects of a 6-week comprehensive circadian optimization intervention Amplify-RHYTHM in patients with diabetic retinopathy. The outcomes of interest are objective and subjective sleep parameters, evening salivary cortisol and melatonin levels, and glucose parameters from continuous glucose monitoring

Circadian Amplification in Diabetic Retinopathy

Circadian Amplification in Diabetic Retinopathy

Condition
Diabetic Retinopathy
Intervention / Treatment

-

Contacts and Locations

Chicago

University of Illinois at Chicago, Chicago, Illinois, United States, 60612

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * type 2 diabetes
  • * a history of at least moderate non-proliferative diabetic retinopathy
  • * would like to improve sleep
  • * own a smartphone compatible with fitbit.
  • * Use of melatonin
  • * Use of antipsychotics
  • * Use of more than one antidepressant. The dose of which needs to be stable for 6 weeks.
  • * illicit drug use
  • * night shift work or travel beyond 2 time zones in the month before enrollment
  • * end stage renal disease requiring renal replacement therapy
  • * history of stroke or transient ischemic attacks
  • * history of dementia or memory impairment
  • * uncontrolled congestive heart failure or recent hospitalization for cardiac condition (6 months)
  • * chronic obstructive pulmonary disease requiring oxygen
  • * severe chronic liver disease such as cirrhosis
  • * ongoing treatment for major medical problems such as cancer
  • * history of severe hypoglycemia defined as hypoglycemic episodes requiring assistance from others within the past six months.
  • * Regular use of sedatives and hypnotics (\>2 times/ month).
  • * clinically significant epiretinal membranes, clinically significant lens opacities, or cystoid macular edema, iris neovascularization, iris atrophy, or an asymmetrically shaped pupil, nuclear sclerotic, posterior subcapsular, or cortical lens opacities greater than 2+, a history of pan-retinal photocoagulation.
  • * Significant depressive symptoms as assessed by PHQ-8 questionnaire (score \>14)
  • * No health insurance coverage
  • * History of untreated severe OSA.
  • * Uncontrolled hypertension (blood pressure ≥ 160/100 mmHg),
  • * Uncontrolled diabetes (A1C ≥ 11%)

Ages Eligible for Study

40 Years to 65 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Illinois at Chicago,

Study Record Dates

2026-06