TRE x ICR: Impact of Time Restricted Eating on Patients With Coronary Artery Disease (CAD) Undergoing Cardiac Rehabilitation

Sponsor
University of California, San Diego (Other)
Overall Status
Recruiting
CT.gov ID
NCT05014880
Collaborator
Salk Institute for Biological Studies (Other), The Cleveland Clinic (Other)
40
1
2
17.9
2.2

Study Details

Study Description

Brief Summary

The purpose of this study is to see if reducing the number of hours during which one eats each day will help reduce levels of LDL cholesterol and improve other markers of metabolic and cardiovascular health (i.e. blood sugar levels and blood pressure). The study also aims to assess changes in exercise capacity and trimethylamine N-oxide (TMAO) levels in response to Time Restricted Eating (TRE) and Intensive Cardiac Rehabilitation (ICR) versus ICR alone. TMAO is a metabolite, or a substance, produced during digestion and metabolism. Preliminary data illustrates a correlation between high levels of TMAO and higher risk of cardiovascular disease and mortality. We will also be looking at participants' long-term cardiovascular health status after they complete the ICR program.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: ICR (Intensive Cardiac Rehabilitation)
  • Behavioral: ICR x TRE (Intensive Cardiac Rehabilitation x Time-Restricted Eating)
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Investigator)
Primary Purpose:
Treatment
Official Title:
Impact of Time Restricted Eating on Exercise Capacity, Cardiometabolic Parameters, and Trimethylamine N-oxide (TMAO) Levels in Patients With Coronary Artery Disease (CAD) Undergoing Cardiac Rehabilitation
Actual Study Start Date :
Sep 2, 2021
Anticipated Primary Completion Date :
Mar 2, 2023
Anticipated Study Completion Date :
Mar 2, 2023

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: ICR (Intensive Cardiac Rehabilitation)

20 patients will be randomly assigned to the standard of care group, which will receive the standard health and nutritional wellness guidelines that are required of UCSD's 9-week ICR program, referred to as the "ICR" group.

Behavioral: ICR (Intensive Cardiac Rehabilitation)
Participants in this arm will not have to adopt a 10-hour eating window while taking part in UCSD's 9-week ICR program.

Experimental: ICR x TRE (Intensive Cardiac Rehabilitation x Time-Restricted Eating)

20 patients will be randomly assigned to the Time-Restricted Eating (TRE) group which will be asked to limit the number of hours they eat in a day to 10 hours in addition to receiving the standard of care health and nutritional wellness guidelines that are required of UCSD's 9-week ICR program, referred to as the "ICR x TRE" group.

Behavioral: ICR x TRE (Intensive Cardiac Rehabilitation x Time-Restricted Eating)
Participants in this arm will adhere to a daily, consistent 10-hour eating window while undergoing UCSD's 9-week ICR program to see if there is an improvement on cardiometabolic parameters.

Outcome Measures

Primary Outcome Measures

  1. Change in Exercise Capacity (MetS) [Baseline and Week 1-9]

    Exercise Capacity

Secondary Outcome Measures

  1. Change in LDL cholesterol [Baseline and Week 9]

    LDL cholesterol (mg/dL)

  2. Change in non-HDL cholesterol [Baseline and Week 9]

    non-HDL cholesterol (mg/dL)

  3. Change in Triglycerides [Baseline and Week 9]

    Triglycerides (mg/dL)

Other Outcome Measures

  1. Change in TMAO levels [Baseline and Week 9]

    TMAO levels (uM)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Age: 18-75 years

  2. Enrollment and planned participation in UC San Diego's 9-week Intensive Cardiac Rehabilitation Program

  3. Established diagnosis of coronary artery disease (concomitant systolic or diastolic HF is allowable)

  4. Own a smartphone (Apple iOS or Android OS)

  5. If patients are on cardiovascular medications (HMG CoA reductase inhibitors (statins), other lipid modifying drugs (including over the counter drugs such as red yeast rice and fish oil), anti-hypertensive, anti-diabetes drugs, no dose adjustments will be allowed during the study period.

Exclusion Criteria:
  1. Taking insulin within the last 6 months.

  2. Known inflammatory and/or rheumatologic disease.

  3. Active tobacco abuse or illicit drug use or history of treatment for alcohol abuse.

  4. Pregnant or breast-feeding women.

  5. Shift workers with variable (e.g. nocturnal) hours.

  6. Caregivers for dependents requiring frequent nocturnal care/sleep interruptions.

  7. Planned international travel during study period.

  8. Systolic HF alone.

  9. Heart transplant within the past 1 year.

  10. Presence of left ventricular assist device.

  11. Uncontrolled arrhythmia (i.e. rate-controlled atrial fibrillation/atrial flutter are not exclusion criteria).

  12. History of thyroid disease requiring dose titration of thyroid replacement medication(s) within the past 3 months (i.e. hypothyroidism on a stable dose of thyroid replacement therapy is not an exclusion).

  13. History of adrenal disease.

  14. History of malignancy undergoing active treatment, except non-melanoma skin cancer.

  15. History of type I diabetes with ongoing insulin dependence.

  16. History of eating disorders.

  17. History of cirrhosis.

  18. History of stage 4 or 5 chronic kidney disease or requiring dialysis.

  19. History of HIV/AIDS.

  20. Currently enrolled in a weight-loss or weight-management program. This does not include UC San Diego's Cardiac Rehabilitation Programs.

  21. On a special or prescribed diet for other reasons (e.g. Celiac disease).

  22. Currently taking any medication that is meant for, or has a known effect on, appetite.

  23. Any history of surgical intervention for weight management.

  24. Uncontrolled psychiatric disorder (including history of hospitalization for psychiatric illness).

  25. Baseline eating window <14 hours per day as documented on mCC app.

  26. Failure to use the smartphone app for documentation (defined as <2 meals/day for ≥3 days during baseline).

Contacts and Locations

Locations

Site City State Country Postal Code
1 Altman Clinical and Translational Research Institute La Jolla California United States 92093

Sponsors and Collaborators

  • University of California, San Diego
  • Salk Institute for Biological Studies
  • The Cleveland Clinic

Investigators

  • Principal Investigator: Pam R Taub, MD, UC San Diego Health

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Pam Taub, MD, Professor of Medicine, University of California, San Diego
ClinicalTrials.gov Identifier:
NCT05014880
Other Study ID Numbers:
  • 200530
First Posted:
Aug 20, 2021
Last Update Posted:
Sep 13, 2021
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Pam Taub, MD, Professor of Medicine, University of California, San Diego
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 13, 2021