Exercise Timing and Postprandial Glucose Responses
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Timed Endurance Exercise, No Exercise Control.
- Who it may be relevant to
- Registry conditions: Exercise Timing, Postprandial Glucose. Basic parameters: 18 years — 35 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Germany
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Exercise Timing and Postprandial Glucose Responses in Healthy Adults
Overview
This interventional crossover study examines the effect of exercise timing relative to meal intake on postprandial glucose responses in healthy, physically active young adults. Participants complete five experimental conditions involving endurance exercise performed before or after breakfast or dinner, as well as a non-exercise control condition, while wearing a continuous glucose monitoring device. Postprandial glucose responses are assessed for the three consecutive meals following each exercise session. Following morning exercise, outcomes are assessed after breakfast, lunch, and dinner on the same day. Following evening exercise, outcomes are assessed after dinner on the same day and after breakfast and lunch on the subsequent day. All meals are standardized and consumed at fixed clock times.
Detailed description
This study is conducted as a repeated measures, randomized crossover trial. Each participant completes five intervention conditions within a 14 day study period while wearing a continuous glucose monitoring device. The order of conditions is randomized, and all participants complete all conditions.
The five conditions include endurance exercise performed before breakfast, after breakfast, before dinner, after dinner, and a recovery day without exercise. On exercise days, participants complete a 45 minute outdoor run at a vigorous intensity at predefined times relative to standardized meals. Breakfast, lunch, and dinner are consumed at fixed clock times (08:00, 13:00, and 18:00, respectively).
Postprandial glucose outcomes are assessed for the three consecutive meals following each exercise session. In conditions involving exercise performed before or after breakfast, outcomes are assessed following breakfast, lunch, and dinner on the same day. In conditions involving exercise performed before or after dinner, outcomes are assessed following dinner on the same day and following breakfast and lunch on the subsequent day.
Dietary intake is fully standardized across all intervention days. Meal composition is identical across intervention days within participants, with macronutrient composition held constant. Meals are designed to have a high glycemic load, calculated using published glycemic index tables and established food composition databases. Meals must be consumed within a predefined consumption window, with the start of meal intake serving as the reference time point for postprandial glucose analyses. Adherence to meal timing and consumption is verified using time-stamped photographs of meals and packaging, along with a standardized checklist documenting consumption times.
Habitual waking times compatible with the fixed breakfast time are required for study participation. During the intervention period, participants are instructed to standardize bedtime as closely as possible across study days and to record wake time and sleep duration daily by self-report. Caffeine consumption is restricted on intervention days and on the day preceding each intervention day. On the day before each intervention day, participants are also instructed to refrain from structured exercise and alcohol. Participants are further instructed to replicate, as closely as possible, the type and timing of meals consumed on the day preceding each intervention condition in order to standardize pre-intervention nutritional status. This applies particularly to the day before conditions involving morning exercise and to earlier meals consumed on days with evening exercise.
All exercise sessions are completed outdoors on the same route. Ambient temperature and precipitation are recorded for each exercise session using smartphone-based weather data. Exercise sessions may be rescheduled in cases of extreme weather conditions or acute illness to ensure participant safety and protocol consistency.
Interventions
- Behavioral Timed Endurance Exercise
The exercise intervention consists of a 45 minute continuous outdoor run performed on a standardized route. Participants are instructed to maintain a consistent running pace across all exercise conditions. Exercise intensity is standardized using a target heart rate corresponding to 75 to 85 percent of maximal heart rate, and participants must be able to complete 45 minutes of continuous running at this intensity without stopping. Heart rate, duration, distance, and pace are recorded using a he - Behavioral No Exercise Control
This intervention involves a non-exercise control condition
Primary outcome measures
- 3-hour postprandial glucose area under the curve (AUC) [Time frame: During each intervention condition within the 14-day study period, assessed over the 3-hour period following each of the three consecutive meals after each condition]
Secondary outcome measures (5)
- Incremental postprandial glucose AUC [Time frame: During each intervention condition within the 14-day study period, assessed over the 3-hour period following each of the three consecutive meals after each condition]
- Peak postprandial glucose concentration [Time frame: During each intervention condition within the 14-day study period, assessed over the 3-hour period following each of the three consecutive meals after each condition]
- Time to peak glucose [Time frame: During each intervention condition within the 14-day study period, assessed over the 3-hour period following each of the three consecutive meals after each condition]
- Subjective appetite ratings [Time frame: Repeatedly during each intervention condition within the 14-day study period, assessed before and after each meal and exercise session]
- Rating of perceived exertion [Time frame: Immediately after each exercise session during each intervention condition within the 14-day study period]
Eligibility criteria
Inclusion criteria
- Age 18 to 35 years
- Body mass index 18.5 to 24.9 kg per square meter
- Able to complete 45 minutes of continuous running at an intensity corresponding to 75 to 85 percent of maximal heart rate without stopping
- Engages in regular endurance-type physical activity
- Habitual waking times are compatible with the fixed breakfast time of 08:00
- Willing and able to comply with all study procedures, including standardized meals, exercise sessions, behavioral restrictions, and continuous glucose monitoring
- For female participants: non-pregnant and using stable hormonal contraception for at least 3 months
Exclusion criteria
- Acute or chronic illness
- Metabolic disorders or conditions associated with altered glucose or lipid metabolism
- Use of medications known to interfere with glucose metabolism or study outcomes
- Intolerance or allergy to components of the standardized study diets
- Pregnancy or breastfeeding
- Body mass index greater than or equal to 25 kg per square meter
- Current or past eating disorder, or any medical condition or medication that could affect appetite regulation, glucose regulation, or make vigorous endurance exercise unsafe
- Current smoking or use of nicotine-containing products
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Crossover
- Masking
- Open label
- Primary purpose
- Other
Study locations
Germany · 1 center
- Technical University of Munich — München
Identifiers
NCT: NCT07434349 · ExTime-Glu