Skip to main content
OpenTrials
Completed

NCT Number: NCT05108987

Exercise and Time of Day in Type 2 Diabetes

The overall purpose of the study is to test the effect exercise time of day in adults with type 2 diabetes or prediabetes. The overarching hypothesis is that afternoon exercise in the afternoon may promote better changes in metabolic and vascular insulin sensitivity. We anticipate that these changes will correlate with glycemic control and blood pressure changes.

Completed

Looking for future studies?

Notify Me

Key information

Age range

30 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

New Jersey Institute for Food, Nutrition, and Health, New Brunswick, New Jersey, United States

Loading trial locations.

About this study

Type 2 diabetes (T2D) is associated with a 3-fold cardiovascular disease (CVD) mortality risk compared with healthy controls, and it is estimated that 30 million adults in the United States have the disease. In recent years the American Diabetes Association (ADA) and American College of Sports Medicine (ACSM) recommend moderate intensity (40-60% heart rate max, HRmax) aerobic exercise 3-5d/wk for the management of T2D. The statement also recognized that higher exercise intensity (>60% HRmax) predicts better blood glucose control than exercise volume. Cardiovascular health (e.g. fitness, blood pressure, etc.) also appears to respond in an exercise dose dependent manner. Despite these suggestions, many people exercising compensate by eating calories back from exercise, thereby negating weight loss. Moreover, compliance and adherence to exercise and diet medical counsel is disappointingly low.

Recent work has begun to target the best time of day to exercise in effort to improve weight loss and related health. This has evolved in part since circadian biology reveals people tend to become glucose intolerant, and develop insulin resistance and endothelial dysfunction in the evening compared with morning. As a result, it would be reasonable to hypothesize that exercise in the afternoon may be best at combating natural declines in health as well as optimizing training adaptations. However, not all studies agree that afternoon is the best time to exercise. In fact, some have demonstrated that 12 wks of aerobic plus resistance exercise improved glycemic control whether performed in the morning or afternoon in adults with T2D. Moreover, consistent morning exercise has been suggested to improve exercise adherence through possible enjoyment as well as lead to greater weight loss. Taken together, additional work is warranted to understand time of day in which exercise is performed given circadian influence may contribute to variations in favorable metabolic as well as vascular adaptation for CVD prevention/treatment. Excitingly, we have preliminary data showing that afternoon exercise induces greater weight loss, reductions in food intake as well as perceptions of appetite and increased insulin sensitivity when compared to morning exercisers. Thus, the overall purpose of this proposal is to determine whether exercise time of day differentially enhances likelihood of weight loss via appetite regulation as well as glycemic control. Our overarching hypothesis is that afternoon exercise will enhance the effectiveness of exercise to induce weight loss, improve appetite and improve glycemic regulation compared to exercise in the morning. Taken together, findings from this study will inform public health recommendations to contemporary behavioral strategies to treat T2D. The study will also provide much needed experimental evidence to time of day in which exercise is performed influences public health risk.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Male or female >30 and <80 years old.
  • Has a body mass index >25 and <45 kg/m2.
  • Previously diagnosed with prediabetes and/or T2D.
  • If not previously diagnosed, has a fasting blood glucose ≥ 100 mg/dL and/or HbA1c ≥ 5.7%

Exclusion criteria

  • Morbidly obese patients (BMI >45 kg/m2) and lean patients (BMI <25 kg/m2)
  • Evidence of type 1 diabetes and diabetics requiring insulin therapy.
  • Subjects who have not been weight stable (>2 kg weight change in past 3 months)
  • Subjects who have been recently active (>30 min of moderate/high intensity exercise, 3 times/week).
  • Subjects who are smokers or who have quit smoking <1 years ago
  • Subjects with abnormal estimated glomerular filtration rate (eGFR).
  • Hypertriglyceridemic (>400 mg/dl) and hypercholesterolemic (>260 mg/dl) subjects
  • Hypertensive (>160/100 mmHg)
  • Subjects with a history of significant metabolic, cardiac, congestive heart failure, cerebrovascular, hematological, pulmonary, gastrointestinal, liver, renal, or endocrine disease or cancer that in the investigator's opinion would interfere with, alter the outcome measures, or impact subject safety.
  • Pregnant (as evidenced by positive urine pregnancy test) or nursing women.
  • Subjects with contraindications to participation in an exercise training program
  • Currently taking active weight suppression medication (e.g. phentermine,orlistat, lorcaserin, naltrexone-bupropion in combination, liraglutide, benzphetamine, diethylpropion, phendimetrazine)
  • Known hypersensitivity to perflutren (contained in Definity)

Treatment and study plan

Morning Exercise

Behavioral

Sixty minutes of supervised exercise at an intensity ~85% VO2max will be performed in the morning (between 7:00am - 11:00am) for up to 10 sessions.

Afternoon exercise

Behavioral

Sixty minutes of supervised exercise at an intensity ~85% VO2max will be performed in the afternoon (between 4:00pm - 8:00pm) for up to 10 sessions.

Primary outcomes

  1. Body Weight

    Time frame: Over the course of 2 weeks.

    The primary outcome is changes in body weight pre- and post-intervention

Secondary outcomes

  1. Glucose Tolerance

    Time frame: Over the course of 2 weeks.

    We will examine the influence of Noom on the glucose area under the curve during the oral glucose tolerance test.

  2. Flow-mediated dilation

    Time frame: Over the course of 2 weeks.

    We will assess blood flow to better understand nutrient/glucose delivery.

Sponsors and collaborators

Lead sponsor

Rutgers, The State University of New Jersey

Other

Registry information

Official study title

Exercise Time of Day for Cardiometabolic Health in Type 2 Diabetes

Important dates

Study start
2021
Primary completion
2025
Study completion
2025
First posted
Nov 5, 2021
Registry last updated
May 18, 2026

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.

Published trials that share one or more normalized conditions with this study.