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Active, Not Recruiting

NCT Number: NCT07203196

Circadian Health Regulation and Optimization for Rejuvenation Outcomes

In this single arm intervention trial, the investigators will assess the impact of a personalized lifestyle plan, centered on supporting biological rhythms, on blood sugar levels, physical, cognitive and immune function in older adults with a habitual eating window of 12 hours or more, and elevated blood glucose levels.

All participants will be provided with a personalized circadian rhythm optimization plan (CRO) centered on improving (1) diet, (2) exercise (3) sleep habits based on their body's natural rhythms. The study includes a 2-week screening/baseline assessments, with follow-up health assessments at 2-months.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

50 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of California San Diego

La Jolla, California, 92037, United States

About this study

The purpose of this study is to assess if modifying lifestyle behaviors such as improving nutrition quality while consolidating caloric intake to a consistent 8-10 hour window, incorporating regular exercise and ensuring a consistent sleep window will help improve glucose (sugar) regulation, physical, cognitive and immune function and improve other markers of metabolic, cardiovascular health and aging (i.e. lipid levels, inflammation markers, etc.).

Circadian clocks ("circa" means approximately and "dia" means day) are daily rhythms in physiology and behavior (activity, sleep, eating pattern) that help the body anticipate and adapt to predictable events in the environment. These rhythms are generated and maintained by biological clocks that are present in the brain and almost every organ. Remarkably, even in the absence of any timing information from a device, the human body can keep track of time and thereby help us eat and sleep at optimum times. However, our lifestyle and work schedules can lead us to eat, exercise, and sleep at times that the clocks in our body are not prepared for. When these abnormal daily patterns continue for several weeks or years, it can affect our health in many ways including increased body weight, poor sleep, and elevated risk for various chronic diseases.

A growing body of preclinical research has shown that synchronizing behaviors, such as food intake, exercise, and light exposure, with the body's biological clock improves skeletal muscle function, cognitive performance, and inflammatory markers. Clinical studies have further validated these findings, showing that circadian-based interventions, such as time-restricted eating (TRE), which restricts all caloric intake to a personalized consistent daily eating window, daytime light exposure and exercise have been shown to improve mood, sleep quality and cardiometabolic health. Despite these promising individual findings, no study has comprehensively examined the combined effects of TRE, structured exercise and optimized sleep schedule as an integrated strategy to restore circadian alignment and reverse key physiological markers of aging in older adults.

In this study, the investigators are interested in evaluating the effects of modifying eating, activity and sleeping patterns on age related health outcomes in older adults with elevated blood sugar levels. All participants will be provided with a personalized circadian rhythm optimization (CRO) program centered on (1) consuming a Mediterranean diet within a personalized 8-10-hour daytime window, (2) increasing daytime light exposure and reducing bright light at night, (3) incorporating 150 minutes of moderate-intensity aerobic exercise each week (4) holding a consistent 7-9 hour sleep schedule (5) taking supplements based on individual needs.

The study is 90-days including a 2-week screening/baseline assessment followed by a 2-week period to developed their personalized plan based off their baseline assessments and finally a 8-week guided intervention period. Health assessments will be taken at screening/baseline, and at 90 days. Assessments will include cognitive function (cognitive assessment battery), physical function (VO2 Max, isometric strength, short physical performance battery), dietary recall (ASA24), blood tests (biomarkers of cardiometabolic health and immune parameters), glycemic regulation (Continuous Glucose Monitors), body composition ( bioelectrical impedance scan), dietary intake (logged on the myCircadianClock smartphone app), sleep and quality of life questionnaires, and activity, sleep, and wrist temperature (actigraphy watch) and subclavian and ankle surface temperature (non-invasive temperature sensor).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age: 50-80 years
  • Fasting glucose ≥ 100 mg/dL or HbA1c > 5.6%
  • Own a smartphone (Apple iOS or Android OS)
  • Proficient in reading and speaking in English
  • An eating window ≥12 hour/day
  • Willing to travel to sports facilities for exercise training sessions
  • Participants on cardiovascular medications (HMG CoA reductase inhibitors (statins), metformin, SLGT2 inhibitors, GLP1 receptor agonists other lipid-modifying drugs (including over-the counter drugs such as red yeast rice and fish oil), anti-hypertensive, drugs), are allowed if on a stable dose for 6-months, but dose adjustments are not allowed during the study

Exclusion criteria

  • Insufficient dietary logging on the mCC app during screening, defined as less than 7 of 14 days of baseline of dietary logging with a minimum of 2 items a day, at least 5 hours apart
  • Type 1 Diabetes or Insulin-dependent Type 2 Diabetes
  • HbA1C > 9.0%
  • Use of sulfonylurea or insulin within the last 3 months (due to unknown safety with TRE)
  • Change in medications that could impact study outcomes within the past 6 months
  • Change in weight of >4kg in the past 3 months
  • Systolic BP greater than 160 mmHg and/or diastolic BP greater than 110 mmHg at rest
  • Fasting LDL cholesterol greater than 250 mg/dL
  • Fasting triglycerides greater than 500g/dL
  • Variable work hours, such as working night shifts
  • Caregiver for a dependent requiring frequent nocturnal care/sleep interruptions
  • Active tobacco use, illicit drug use, or history of treatment for alcohol abuse in the past 5 years.
  • Travel involving a time zone change of more than 3 hours twice or more during the study period
  • Active treatment for inflammatory and/or rheumatologic disease
  • History of a major adverse cardiovascular event within the past year (acute coronary syndrome, percutaneous coronary intervention, coronary artery bypass graft surgery, hospitalization for congestive heart failure, stroke/transient ischemic attack)
  • Uncontrolled arrhythmia (i.e. rate-controlled atrial fibrillation/atrial flutter are acceptable)
  • Previously diagnosed with sever aortic stenosis
  • Previously diagnosed with sever COPD (FEV1/FVC ratio <.7 & FEV1 (%predicted) <49
  • Orthopedic impairments severely compromising exercise performance
  • BMI <18.5 kg/m2
  • History of thyroid disease requiring dose titration of thyroid replacement medication(s) within the past 6 months (i.e. hypothyroidism on a stable dose of thyroid replacement therapy is not an exclusion).
  • History of adrenal disease in the past 5 years
  • History of malignancy undergoing active treatment, except non-melanoma skin cancer, in the past 5 years
  • History of an eating disorder in the past 5 years
  • History of cirrhosis in the past 5 years
  • History of stage 4 or 5 chronic kidney disease or dialysis in the past 5 years
  • History of HIV/AIDs
  • Currently enrolled in weight-loss or weight-management program
  • Regularly engages in 100 minutes or more of structured exercise
  • VO2 max threshold is above average for that individuals age group [78]
  • Uncontrolled psychiatric disorder including prior hospitalization

Treatment and study plan

Circadian Rhythm Optimization

Behavioral

Participants will follow a Mediterranean diet while consuming all calories within a personalized 8-10 hour daytime window. They will increase daytime light exposure to at least one hour per day, engage in a minimum of 150 minutes of moderate-intensity aerobic exercise each week (including at least two sessions lasting no less than 60 minutes), maintain a consistent 7-9 hour sleep schedule, and take supplements as recommended based on individual needs. Participants will also record all food and beverage intake, as well as exercise, using the myCircadianClock app.

Primary outcomes

  1. HbA1c (%)

    Time frame: Baseline and 90 days

    HbA1c levels (%) as assessed by fasting blood draw

Secondary outcomes

  1. Grip Strength

    Time frame: Baseline and 90 days

    Maximal grip force (Kg)

  2. Isometric Knee Strength

    Time frame: Baseline and 90 days

    Maximal force output for knee flexion and extension (Kg)

  3. VO2 Max

    Time frame: Baseline and 90 days

    Maximal oxygen consumption (mL/kg/min).

  4. Time to 85% of Age Predicted Maximal Heart Rate

    Time frame: Baseline and 90 days

    Time to 85% of age predicted maximal heart rate (mins).

  5. Flanker Inhibitory and Control and Attention Test (Fully-Corrected T-score)

    Time frame: Baseline and 90 days

    Flanker Inhibitory and Control and Attention Test (Fully-Corrected T-score) assessed through NIH cognitive assessment battery. The score compares an individual's cognitive performance to a nationally representative norming sample correcting for age, sex, race/ethnicity, and educational attainment.

  6. Dimensional Change Card Sort (Fully-Corrected T-score)

    Time frame: Baseline and 90 days

    Dimensional Change Card Sort (Fully-Corrected T-score) assessed through NIH cognitive assessment battery. The score compares an individual's cognitive performance to a nationally representative norming sample correcting for age, sex, race/ethnicity, and educational attainment.

  7. Pattern Comparison Processing Speed Test (Fully-Corrected T-score)

    Time frame: Baseline and 90 days

    Pattern Comparison Processing Speed Test (Fully-Corrected T-score) assessed through NIH cognitive assessment battery. The score compares an individual's cognitive performance to a nationally representative norming sample correcting for age, sex, race/ethnicity, and educational attainment.

  8. Picture Sequence Memory test (Fully-Corrected T-score)

    Time frame: Baseline and 90 days

    Picture Sequence Memory test (Fully-Corrected T-score) assessed through NIH cognitive assessment battery. The score compares an individual's cognitive performance to a nationally representative norming sample correcting for age, sex, race/ethnicity, and educational attainment.

  9. Trail Making Test

    Time frame: Baseline and 90 days

    Trail making test part A and B will be assessed by the time to completion (seconds) for each assessment.

  10. Glucagon (pg/mL)

    Time frame: Baseline and 90 days

    Glucagon (pg/mL) assessed through fasting blood draw

  11. Leptin (ng/mL)

    Time frame: Baseline and 90 days

    Leptin (ng/mL) assessed through fasting blood draw

  12. IL-1α (pg/mL)

    Time frame: Baseline and 90 days

    IL-1α (pg/mL) assessed through fasting blood draw

  13. IL-1β (pg/mL)

    Time frame: Baseline and 90 days

    IL-1β (pg/mL)assessed through fasting blood draw

  14. IL-2 (pg/mL)

    Time frame: Baseline and 90 days

    IL-2 (pg/mL) assessed through fasting blood draw

  15. IL-3 (pg/mL)

    Time frame: Baseline and 90 days

    IL-3 (pg/mL) assessed through fasting blood draw

  16. IL-4 (pg/mL)

    Time frame: Baseline and 90 days

    IL-4 (pg/mL) assessed through fasting blood draw

  17. IL-5 (pg/mL)

    Time frame: Baseline and 90 days

    IL-5 (pg/mL) assessed through fasting blood draw

  18. IL-6 (pg/mL)

    Time frame: Baseline and 90 days

    IL-6 (pg/mL) assessed through fasting blood draw

  19. IL-7 (pg/mL)

    Time frame: Baseline and 90 days

    IL-7 (pg/mL) assessed through fasting blood draw

  20. IL-8

    Time frame: Baseline and 90 days

    IL-8 (pg/mL) assessed through fasting blood draw

  21. IL-9 (pg/mL)

    Time frame: Baseline and 90 days

    IL-9 (pg/mL) assessed through fasting blood draw

  22. IL-10 (pg/mL)

    Time frame: Baseline and 90 days

    IL-10 (pg/mL) assessed through fasting blood draw

  23. IL-12p70 (pg/mL)

    Time frame: Baseline and 90 days

    IL-12p70 (pg/mL) assessed through fasting blood draw

  24. IL-13 (pg/mL)

    Time frame: Baseline and 90 days

    IL-13 (pg/mL) assessed through fasting blood draw

  25. IL-15 (pg/mL)

    Time frame: Baseline and 90 days

    IL-15 (pg/mL) assessed through fasting blood draw

  26. IL-16 (pg/mL)

    Time frame: Baseline and 90 days

    IL-16 (pg/mL) assessed through fasting blood draw

  27. IL-17A (pg/mL)

    Time frame: Baseline and 90 days

    IL-17A (pg/mL) assessed through fasting blood draw

  28. IL-17F (pg/mL)

    Time frame: Baseline and 90 days

    IL-17F (pg/mL) assessed through fasting blood draw

  29. IL-18 (pg/mL)

    Time frame: Baseline and 90-days

    IL-18 (pg/mL) assessed through fasting blood draw

  30. IL-20 (pg/mL)

    Time frame: Baseline and 90 days

    IL-20 (pg/mL) assessed through fasting blood draw

  31. IL-21 (pg/mL)

    Time frame: Baseline and 90 days

    IL-21 (pg/mL) assessed through fasting blood draw

  32. IL-22 (pg/mL)

    Time frame: Baseline and 90 days

    IL-22 (pg/mL) assessed through fasting blood draw

  33. IL-23 (pg/mL)

    Time frame: Baseline and 90 days

    IL-23 (pg/mL) assessed through fasting blood draw

  34. IL-27 (pg/mL)

    Time frame: Baseline and 90 days

    IL-27 (pg/mL) assessed through fasting blood draw

  35. IL-28 (pg/mL)

    Time frame: Baseline and 90 days

    IL-28 (pg/mL) assessed through fasting blood draw

  36. IL-33 (pg/mL)

    Time frame: Baseline and 90 days

    IL-33 (pg/mL) assessed through fasting blood draw

  37. MCP-1 (pg/mL)

    Time frame: Baseline and 90 days

    MCP-1 (pg/mL) assessed through fasting blood draw

  38. MCP-2

    Time frame: Baseline and 90 days

    MCP-2 (pg/mL) assessed through fasting blood draw

  39. MCP-3 (pg/mL)

    Time frame: Baseline and 90 days

    MCP-3 (pg/mL) assessed through fasting blood draw

  40. MCP-4 (pg/mL)

    Time frame: Baseline and 90 days

    MCP-4 (pg/mL) assessed through fasting blood draw

  41. TGFα (pg/mL)

    Time frame: Baseline and 90 days

    TGFα (pg/mL) assessed through fasting blood draw

  42. TNFβ (pg/mL)

    Time frame: Baseline and 90 days

    TNFβ (pg/mL) assessed through fasting blood draw

  43. EGF (pg/mL)

    Time frame: Baseline and 90 days

    EGF (pg/mL) assessed through fasting blood draw

  44. TNF-α (pg/mL)

    Time frame: Baseline and 90 days

    TNF-α (pg/mL) assessed through fasting blood draw

  45. Ghrelin (pg/mL)

    Time frame: Baseline and 90-days

    Ghrelin (pg/mL) assessed through fasting blood draw

  46. IGF-1 (ng/mL)

    Time frame: Baseline and 90 days

    IGF-1 (ng/mL) assessed through fasting blood draw

  47. IGF-2 (ng/mL)

    Time frame: Baseline and 90 days

    IGF-2 (ng/mL) assessed through fasting blood draw

  48. IL-1RA (pg/mL)

    Time frame: Baseline and 90 days

    IL-1RA (pg/mL) assessed through fasting blood draw

  49. TRAIL (pg/mL)

    Time frame: Baseline and 90 days

    TRAIL (pg/mL) assessed through fasting blood draw

  50. VEGF-A (pg/mL)

    Time frame: Baseline and 90 days

    VEGF-A (pg/mL) assessed through fasting blood draw

  51. IGFBP-1 (ug/mL)

    Time frame: Baseline and 90 days

    IGFBP-1 (ug/mL) assessed through fasting blood draw

  52. GIP (pg/mL)

    Time frame: Baseline and 90-days

    GIP(pg/mL) assessed through fasting blood draw

  53. GLP-1 (pmol/L)

    Time frame: Baseline and 90 days

    GLP-1 (pmol/L) assessed through fasting blood draw.

  54. Total Recall (T-score)

    Time frame: Baseline and 90-days

    Total Recall (T-score) as assessed through Hopkins Verbal Learning Test - Revised. T-score is adjusted for participant's age.

  55. Delayed Recall (T-score)

    Time frame: Baseline and 90-days

    Delayed Recall (T-score) as assessed through Hopkins Verbal Learning Test. T-score is adjusted for participant's age.

  56. Retention Percentage (T-score)

    Time frame: Baseline and 90-days

    Retention Percentage (T-score) as assessed through Hopkins Verbal Learning Test - Revised. T-score is adjusted for participant's age.

  57. Recognition Discrimination Index (T-score)

    Time frame: Baseline and 90-days

    Recognition discrimination index as assessed through Hopkins Verbal Learning Test-Revised. T-score is adjusted for participant's age.

  58. Cognition Fluid Composite (Fully-Corrected T-score)

    Time frame: Baseline and 90-days

    Cognition Fluid Composite (Fully-Corrected T-score) as assessed through a composite score of several tests, namely the Flanker inhibitory control and attention test, the dimensional change card sort test, the picture sequence memory test, the list sorting working memory test, and the pattern comparison processing speed test. The score compares an individual's cognitive performance to a nationally representative norming sample correcting for age, sex, race/ethnicity, and educational attainment.

Other outcomes

  1. Total Body Fat Mass (kg)

    Time frame: Baseline and 90 days

    Total Body Fat Mass (kg) assessed by bioelectrical impedance scan

  2. Fat Free Mass

    Time frame: Baseline and 90 days

    Whole body fat free mass (kg) assessed by bioelectrical impedance scan

  3. Intra-Daily Glycemic Variability: CONGA (A.U.)

    Time frame: Baseline and 90-days

    Continuous Overall Net Glycemic Action (CONGA) assessed via continuous glucose monitor

  4. Inter-Daily Glycemic Variability: MODD (mg/dL)

    Time frame: Baseline and 90 days

    Mean of Daily Differences (MODD) assessed via continuous glucose monitor

  5. Glycemic Variability: MAGE (mg/dL)

    Time frame: Baseline and 90 days

    Mean Amplitude of Glycemic Excursions (MAGE) assessed by continuous glucose monitor

  6. Mean Glucose (mg/dL)

    Time frame: Baseline and 90 days

    Mean Glucose assessed by continuous glucose monitor

  7. Fasting Glucose

    Time frame: Baseline and 90 days

    Fasting Glucose (mg/dL) assessed through fasting blood draw

  8. Fasting Insulin

    Time frame: Baseline and 90 days

    Fasting insulin (μU/mL) assessed through fasting blood draw

  9. HOMA-IR

    Time frame: Baseline and 90 days

    HOMA-IR assessed through fasting blood draw

  10. Skin Surface Temperature

    Time frame: Baseline and 90 days

    Mean daily Skin surface temperature at the wrist, ankle and subclavian region of the chest (Degrees C) assessed through actigraphy watch and non-invasive skin temperature probe.

  11. Short Physical Performance Battery

    Time frame: Baseline and 90 days

    A sum of the scores from the Chair Stand Test , Gait Speed Test, Side-By-Side- Stand, Semi-Tandem Stand & Tandem Stand Balance Tests. The scoring for each assessment will be based off the previously established and widely used Short Physical Performance Battery Protocol and score sheet where the Chair Stand Test , Gait Speed Test and balance tests scoring are based off the participants ability to rise from the chair, duration is takes to cover 4m distance (seconds) and duration they are able to balance (seconds) respectively.

  12. Quality of Life Assessment

    Time frame: Baseline and 90 days

    Short-Form 36 (SF-36) Survey. Scores range from 0-100 (an average of all questions which each have a 0-100 scale), with 100 indicating better physical and emotional health.

  13. Triglycerides (mg/dL)

    Time frame: Baseline and 90 days

    Triglycerides (mg/dL) from fasted blood draw.

  14. Total Cholesterol (mg/dL)

    Time frame: Baseline and 90 days

    Total cholesterol (mg/dL) from fasted blood draw.

  15. HDL-cholesterol (mg/dL)

    Time frame: Baseline and 90 days

    HDL-cholesterol (mg/dL) from fasted blood draw.

  16. hs-CRP (mg/dL)

    Time frame: Baseline and 90 days

    hs-CRP (mg/dL) from a fasted blood draw.

  17. LDL Particle number (nmol/L)

    Time frame: Baseline and 90 days

    LDL Particle number (nmol/L) assessed by NMR lipoprotein profiles from a fasted blood draw.

  18. Apo A (mg/dL)

    Time frame: Baseline and 90 days

    Apo A (mg/dL) assessed by NMR lipoprotein profiles from a fasted blood draw.

  19. Apo B (mg/dL)

    Time frame: Baseline and 90 days

    Apo B (mg/dL) assessed by NMR lipoprotein profiles from a fasted blood draw.

  20. Apo A/B ratio

    Time frame: Baseline and 90 days

    Apo A/B ratio assessed by NMR lipoprotein profiles from a fasted blood draw.

  21. Very Low Density Lipoprotein (VLDL) Size (nm)

    Time frame: Baseline and 90 days

    VLDL size (nm) assessed by NMR lipoprotein profiles from a fasted blood draw.

  22. HDL Particle number (umol/L)

    Time frame: Baseline and 90 days

    HDL Particle number (umol/L) assessed by NMR lipoprotein profiles from a fasted blood draw.

  23. Thyroid-Stimulating Hormone (µU/mL)

    Time frame: Baseline and 90 days

    Thyroid-Stimulating Hormone (µU/mL) assessed through fasting blood draw

  24. Sex Hormone Binding Globulin (nmol/L)

    Time frame: Baseline and 90 days

    Sex Hormone Binding Globulin (nmol/L) assessed through fasting blood draw

  25. Gamma-Glutamyl Transferase (IU/L)

    Time frame: Baseline and 90 days

    Gamma-Glutamyl Transferase (IU/L) assessed through fasting blood draw

  26. Cystatin C (mg/L)

    Time frame: Baseline and 90 days

    Cystatin C (mg/L) assessed through fasting blood draw

  27. N-terminal pro-B-type natriuretic peptide (pg/mL)

    Time frame: Baseline and 90 days

    N-terminal pro-B-type natriuretic peptide (pg/mL) assessed through fasting blood draw

  28. Vitamin D

    Time frame: Baseline and 90-days

    Vitamin D levels (ng/mL) assessed through fasting blood draw.

Sponsors and collaborators

Lead sponsor

Salk Institute for Biological Studies

Other

Collaborators

  • University of California, San Diego

Registry information

Official study title

Circadian Health Regulation and Optimization for Rejuvenation Outcomes: The CHRONO Study

Acronym: CHRONO

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Oct 2, 2025
Registry last updated
Dec 31, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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