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Exercise Timing and Postprandial Glucose Responses

Exercise Timing and Postprandial Glucose Responses in Healthy Adults

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07434349
Acronym
ExTime-Glu
Enrollment
30
Registered
2026-02-25
Start date
2026-04-01
Completion date
2026-08-01
Last updated
2026-04-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Exercise Timing, Postprandial Glucose

Keywords

Exercise Timing, Postprandial Glucose, Continuous Glucose Monitoring, Endurance Exercise, Glycemic Response

Brief summary

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

BEHAVIORALTimed 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 heart rate monitor and GPS enabled device. Ambient temperature and precipitation are recorded for each session. Exercise sessions may be rescheduled in cases of extreme weather or acute illness.

This intervention involves a non-exercise control condition

Sponsors

Technical University of Munich
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
3-hour postprandial glucose area under the curve (AUC)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 conditionThe area under the curve for interstitial glucose concentration during the 3-hour period following each of the three consecutive meals assessed after each exercise or control condition, measured using continuous glucose monitoring.

Secondary

MeasureTime frameDescription
Incremental postprandial glucose AUCDuring each intervention condition within the 14-day study period, assessed over the 3-hour period following each of the three consecutive meals after each conditionIncremental area under the curve for interstitial glucose concentration during the 3-hour postprandial period following each assessed meal, calculated relative to pre-meal baseline glucose concentration.
Peak postprandial glucose concentrationDuring each intervention condition within the 14-day study period, assessed over the 3-hour period following each of the three consecutive meals after each conditionMaximum interstitial glucose concentration following each meal.
Time to peak glucoseDuring each intervention condition within the 14-day study period, assessed over the 3-hour period following each of the three consecutive meals after each conditionTime from meal initiation to peak interstitial glucose concentration.
Subjective appetite ratingsRepeatedly during each intervention condition within the 14-day study period, assessed before and after each meal and exercise sessionSubjective sensations of hunger, fullness, prospective food consumption, desire to eat, nausea, and thirst are assessed using electronic 100-mm visual analog scales administered before and after each meal and each exercise session.
Rating of perceived exertionImmediately after each exercise session during each intervention condition within the 14-day study periodPerceived exertion following each exercise session is assessed using the Borg Rating of Perceived Exertion scale (6-20).

Countries

Germany

Contacts

CONTACTChristoph Höchsmann, PD Dr.
christoph.hoechsmann@tum.de+49 89 289 24488
CONTACTKarsten Köhler, Prof. Dr.
karsten.koehler@tum.de
PRINCIPAL_INVESTIGATORChristoph Höchsmann, PD Dr.

Technical University of Munich

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 21, 2026