One-Minute Exercise Snacks and Daytime Glucose in Adults With Type 2 Diabetes
Type 2 Diabetes Mellitus
What this study involves
The registry does not currently label this study as recruiting. Ask about its status before planning a screening visit.
- Study type
- Interventional
- Phase
- Not applicable
- Age range
- 35 years - 75 years
- Sex eligible
- All sexes
- Healthy volunteers
- Not accepted
- Participants
- 40 Actual
These are starting points, not an eligibility decision. The research team must review the full requirements.
About the research
This randomized crossover trial investigated whether brief, one-minute bouts of exercise, known as "exercise snacks," could improve daytime blood glucose levels in adults with type 2 diabetes who were not receiving insulin treatment. The study also examined whether increasing the number of daily exercise snacks provided additional benefits for blood glucose control.
Participants were randomly assigned to different sequences of four experimental conditions: no prescribed exercise snacks (CON), four exercise snacks per day (ES4), six exercise snacks per day (ES6), and eight exercise snacks per day (ES8). Each condition lasted two consecutive days, with a washout period of at least 72 hours between conditions. Each exercise snack consisted of one minute of vigorous body-weight movements. Three exercise sessions were scheduled after meals, while additional sessions were performed at other times of the day.
Participants followed standardized meal plans and wore continuous glucose monitoring devices to measure glucose levels throughout the study. The primary outcome was mean daytime sensor glucose from 6:00 AM to midnight. Additional assessments included glucose variability, post-meal glucose responses, physical activity, exercise adherence, participant acceptability, and safety.
The researchers hypothesized that at least one exercise snack condition would reduce daytime glucose compared with the control condition, while additional daily exercise sessions might not necessarily produce greater glucose-lowering benefits. The findings were intended to inform practical, time-efficient exercise recommendations for adults with type 2 diabetes.
Read the full description
This study was designed as a single-center, randomized, four-condition, four-period crossover trial using a Williams balanced design to evaluate the effects of different daily frequencies of one-minute exercise snacks on glucose regulation in adults with type 2 diabetes who were not treated with insulin.
Study Design and Procedures The study employed four experimental conditions: CON (no prescribed exercise snacks), ES4 (four exercise snacks per day), ES6 (six exercise snacks per day), and ES8 (eight exercise snacks per day). Participants were randomly allocated to one of four Williams balanced intervention sequences, ensuring that each condition appeared once in each experimental period and balancing potential first-order carryover effects.
Before randomization, participants underwent baseline clinical assessments, habitual physical activity monitoring, dietary assessment, and supervised exercise familiarization. Each experimental condition was implemented for two consecutive days, separated by washout periods of at least 72 hours. The four experimental periods were scheduled to be completed over approximately four weeks.
Exercise Snack Interventions Each exercise snack consisted of four consecutive 15-second body-weight exercises, totaling one minute of vigorous physical activity. The exercise combinations included movements such as jumping jacks, squats, high knees, lunges, and modified burpees. Exercise intensity was targeted at 7-9 on the Borg CR-10 rating of perceived exertion scale.
In all three exercise conditions, three exercise snacks were performed approximately 45 minutes after the beginning of breakfast, lunch, and dinner. Additional sessions were distributed across predefined non-postprandial time windows. The ES4 condition included one additional non-postprandial session, ES6 included three, and ES8 included five. Non-postprandial exercise windows were balanced across participants using a Latin-square allocation scheme.
Participants performed the prescribed exercises independently in their usual living or working environments. Exercise adherence and intensity were monitored through electronic exercise logs, Polar H10 heart-rate recordings, mobile reminders, and daily remote follow-up.
Dietary Standardization and Glucose Monitoring During all experimental conditions, participants consumed standardized individualized meals with consistent energy and macronutrient composition. Antidiabetic medication regimens were maintained without changes, and participants were instructed to avoid additional structured exercise.
Glucose concentrations were monitored using a blinded continuous glucose monitoring system (FreeStyle Libre Pro), which recorded interstitial glucose at 15-minute intervals. Participants could not access real-time glucose readings during monitoring.
Outcome Assessment The primary outcome was mean daytime sensor glucose measured from 06:00 to 24:00, averaged across the two observation days of each experimental condition.
Secondary assessments included 24-hour and nighttime mean glucose, non-postprandial daytime glucose, glucose variability, time in predefined glucose ranges, postprandial glucose responses, exercise adherence and intensity, acceptability, habitual physical activity, and adverse events.
Statistical Analysis Linear mixed-effects models were specified to compare glucose outcomes across experimental conditions, accounting for treatment condition, experimental period, randomized sequence, and repeated measurements within participants.
The primary hypothesis was that at least one exercise snack condition would reduce mean daytime glucose compared with the control condition. Additional exploratory analyses examined the shape of the exercise frequency-response relationship and glucose responses following individual exercise snacks performed during postprandial and non-postprandial periods.
The study was intended to provide evidence regarding the optimal daily frequency and practical implementation of brief exercise interventions for improving glucose management in adults with type 2 diabetes.
Who may be able to participate?
The list below is the sponsor’s full registry wording. It can include conditions, prior treatment, test results and other requirements. A match in search does not mean you qualify.
Inclusion Criteria:
1. Adults aged 35-75 years.
2. Diagnosis of type 2 diabetes mellitus for at least 6 months.
3. Glycated hemoglobin (HbA1c) level between 6.5% and 9.0% at screening.
4. Not receiving insulin therapy.
5. Stable glucose-lowering medication regimen for at least 3 months before enrollment.
6. Physically inactive, defined as less than 150 minutes per week of moderate-to-vigorous physical activity, assessed using the Chinese version of the International Physical Activity Questionnaire-Short Form (IPAQ-SF).
7. Able to independently perform body-weight exercises, including jumping jacks, squats, and high knees.
8. Able to use a smartphone and willing to wear a continuous glucose monitoring (CGM) sensor and a heart-rate chest strap.
9. Willing to participate voluntarily and provide written informed consent.
Exclusion Criteria:
1. Current use of insulin, sulfonylureas, or meglitinides.
2. Recent history of severe hypoglycemia or hypoglycemia unawareness.
3. Unstable cardiovascular disease, including unstable angina, acute ischemic changes on a resting electrocardiogram, decompensated heart failure (New York Heart Association class III-IV), uncontrolled severe arrhythmias, symptomatic severe aortic stenosis, acute myocarditis or pericarditis, or other cardiovascular conditions considered absolute contraindications to vigorous exercise.
4. Myocardial infarction or stroke within the preceding 6 months.
5. Uncontrolled severe hypertension (blood pressure ≥180/110 mmHg).
6. Severe proliferative diabetic retinopathy.
7. Active diabetic foot disease or severe peripheral neuropathy.
8. Estimated glomerular filtration rate (eGFR) \<30 mL/min/1.73 m² or severe hepatic dysfunction, defined as alanine aminotransferase (ALT) \>3 times the upper limit of normal.
9. Pregnancy, breastfeeding, or planned pregnancy.
10. Shift work or markedly irregular sleep-wake schedules.
11. Any other condition that, in the investigator's judgment, made the individual unsuitable for participation in the study.
Treatment, groups and participation
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- Assignment
- Random assignment
- Masking
- Single masked
Sequence 1: CON-ES4-ES8-ES6
Participants received four experimental conditions in the following order: CON (no prescribed exercise snacks), ES4 (four 1-minute exercise snacks per day), ES8 (eight 1-minute exercise snacks per day), and ES6 (six 1-minute exercise snacks per day). Each condition lasted two consecutive days, with washout periods of at least 72 hours between conditions.
Behavioral: 1-Minute Exercise Snacks
Sequence 2: ES4-ES6-CON-ES8
Participants received four experimental conditions in the following order: ES4 (four 1-minute exercise snacks per day), ES6 (six 1-minute exercise snacks per day), CON (no prescribed exercise snacks), and ES8 (eight 1-minute exercise snacks per day). Each condition lasted two consecutive days, with washout periods of at least 72 hours between conditions.
Behavioral: 1-Minute Exercise Snacks
Sequence 3: ES6-ES8-ES4-CON
Participants received four experimental conditions in the following order: ES6 (six 1-minute exercise snacks per day), ES8 (eight 1-minute exercise snacks per day), ES4 (four 1-minute exercise snacks per day), and CON (no prescribed exercise snacks). Each condition lasted two consecutive days, with washout periods of at least 72 hours between conditions.
Behavioral: 1-Minute Exercise Snacks
Sequence 4: ES8-CON-ES6-ES4
Participants received four experimental conditions in the following order: ES8 (eight 1-minute exercise snacks per day), CON (no prescribed exercise snacks), ES6 (six 1-minute exercise snacks per day), and ES4 (four 1-minute exercise snacks per day). Each condition lasted two consecutive days, with washout periods of at least 72 hours between conditions.
Behavioral: 1-Minute Exercise Snacks
1-Minute Exercise Snacks BEHAVIORAL
Participants performed vigorous 1-minute exercise snacks consisting of four consecutive 15-second body-weight movements without rest. Exercises included jumping jacks, squats, high knees, lunges, and modified burpees. Individualized exercise combinations were determined during familiarization and remained unchanged across conditions. Target intensity was 7-9 on the Borg CR-10 scale.
Three exercise frequencies were evaluated: ES4 (4 sessions/day: 3 after meals and 1 non-postprandial), ES6 (6 sessions/day: 3 after meals and 3 non-postprandial), and ES8 (8 sessions/day: 3 after meals and 5 non-postprandial). Postprandial exercise was scheduled approximately 45 minutes after meal initiation. Each condition lasted 2 consecutive days, with washout periods of at least 72 hours. Exercise was performed independently, with adherence monitored using heart-rate recordings and electronic logs.
What researchers are measuring
Outcome measures describe what is being studied. They are not proof that a treatment works.
Primary measures
Mean Daytime Sensor Glucose (06:00-24:00)
Time frame: Days 1-2 of each of the four experimental conditions (06:00-24:00 daily), across approximately 4 weeks.
Mean interstitial glucose concentration (mmol/L) measured using a blinded continuous glucose monitoring (CGM) system (FreeStyle Libre Pro). Daytime glucose was defined as the average sensor glucose concentration recorded between 06:00 and 24:00 on each observation day. The primary outcome was calculated as the mean daytime sensor glucose across the two consecutive observation days within each experimental condition (CON, ES4, ES6, and ES8). Glucose measurements were recorded at 15-minute intervals.
Secondary measures
Mean 24-Hour Sensor Glucose
Time frame: Days 1-2 of each of the four experimental conditions (approximately 4 weeks in total).
Mean sensor glucose concentration (mmol/L) measured using blinded continuous glucose monitoring (CGM) from 00:00 to 24:00, averaged across the two observation days of each condition.
Mean Nighttime Sensor Glucose
Time frame: Days 1-2 of each of the four experimental conditions (approximately 4 weeks in total).
Mean CGM-derived sensor glucose concentration (mmol/L) between 00:00 and 06:00, averaged across the two observation days of each experimental condition.
Mean Non-Postprandial Daytime Sensor Glucose
Time frame: Days 1-2 of each of the four experimental conditions (approximately 4 weeks in total).
Mean sensor glucose concentration (mmol/L) during the 12 non-postprandial daytime hours, excluding the three designated 2-hour postprandial windows from 06:00 to 24:00, averaged across two observation days per condition.
Standard Deviation of Sensor Glucose
Time frame: Days 1-2 of each of the four experimental conditions (approximately 4 weeks in total).
Standard deviation (SD) of glucose concentrations (mmol/L) derived from CGM readings during each experimental condition, representing absolute glycemic variability.
Coefficient of Variation of Sensor Glucose
Time frame: Days 1-2 of each of the four experimental conditions (approximately 4 weeks in total).
Coefficient of variation (CV, %) of CGM-derived glucose, calculated as 100 multiplied by the glucose standard deviation divided by the mean glucose concentration for each condition.
Mean Amplitude of Glycemic Excursions
Time frame: Days 1-2 of each of the four experimental conditions (approximately 4 weeks in total).
Mean amplitude of glycemic excursions (MAGE, mmol/L) calculated from CGM recordings according to the prespecified Service method to characterize glucose fluctuations.
Time in Range (3.9-10.0 mmol/L)
Time frame: Days 1-2 of each of the four experimental conditions (approximately 4 weeks in total).
Percentage of valid CGM monitoring time during which sensor glucose concentrations were within the target range of 3.9-10.0 mmol/L.
Time in Tight Range (3.9-7.8 mmol/L)
Time frame: Days 1-2 of each of the four experimental conditions (approximately 4 weeks in total).
Percentage of valid CGM monitoring time during which sensor glucose concentrations were within the tighter glucose range of 3.9-7.8 mmol/L.
Time Above Range (>10.0 mmol/L)
Time frame: Days 1-2 of each of the four experimental conditions (approximately 4 weeks in total).
Percentage of valid CGM monitoring time during which sensor glucose concentrations exceeded 10.0 mmol/L.
Time Below Range (<3.9 mmol/L)
Time frame: Days 1-2 of each of the four experimental conditions (approximately 4 weeks in total).
Percentage of valid CGM monitoring time during which sensor glucose concentrations were below 3.9 mmol/L.
Mean Postprandial Sensor Glucose
Time frame: 0-120 minutes after breakfast, lunch, and dinner on Days 1-2 of each of the four experimental conditions.
Mean CGM-derived glucose concentration (mmol/L) during the 0-120-minute period following the first bite of each meal, evaluated for breakfast, lunch, and dinner.
Peak Postprandial Sensor Glucose
Time frame: 0-120 minutes after breakfast, lunch, and dinner on Days 1-2 of each of the four experimental conditions.
Maximum CGM-derived glucose concentration (mmol/L) observed within 120 minutes after the first bite of breakfast, lunch, or dinner.
Postprandial Incremental Glucose Area Under the Curve
Time frame: 0-120 minutes after breakfast, lunch, and dinner on Days 1-2 of each of the four experimental conditions.
Incremental glucose area under the curve (iAUC, mmol/L × min) from 0 to 120 minutes after meal initiation, calculated by the trapezoidal method using the mean of the readings at meal initiation and 15 minutes before the meal as baseline. Areas below baseline were excluded.
Self-Reported Completed Exercise Snacks per Day
Time frame: Days 1-2 of the ES4, ES6, and ES8 conditions, across approximately 4 weeks.
Mean daily number of prescribed exercise snacks reported as completed in electronic exercise logs, calculated separately for the ES4, ES6, and ES8 conditions.
Heart-Rate-Verified Exercise Snacks per Day
Time frame: Days 1-2 of the ES4, ES6, and ES8 conditions, across approximately 4 weeks.
Mean daily number of self-reported exercise snacks verified by synchronized Polar H10 heart-rate records, with matching completion times within ±10 minutes and a heart-rate rise consistent with a 1-minute exercise bout.
Delivered Exercise Snack Dose per Day
Time frame: Days 1-2 of the ES4, ES6, and ES8 conditions, across approximately 4 weeks.
Mean daily number of exercise snacks meeting the protocol-defined level-3 verification criteria, requiring heart-rate-confirmed completion and achievement of the prespecified intensity threshold. The count was averaged over the two observation days of each exercise condition.
Self-Reported Exercise Completion Rate
Time frame: Days 1-2 of the ES4, ES6, and ES8 conditions, across approximately 4 weeks.
Percentage of prescribed exercise snack sessions reported as completed in the electronic exercise log, calculated separately for each exercise condition.
Rating of Perceived Exertion During Exercise Snacks
Time frame: Each prescribed exercise session on Days 1-2 of the ES4, ES6, and ES8 conditions, across approximately 4 weeks.
Perceived exertion recorded after each exercise snack using the Borg CR-10 scale (0-10), with higher scores indicating greater perceived exertion. The prescribed target was 7-9.
Peak Heart Rate During Exercise Snacks
Time frame: Each prescribed exercise session on Days 1-2 of the ES4, ES6, and ES8 conditions, across approximately 4 weeks.
Maximum heart rate (beats per minute) recorded using a Polar H10 chest strap during each exercise snack.
Peak Heart Rate as a Percentage of Age-Predicted Maximum
Time frame: Each prescribed exercise session on Days 1-2 of the ES4, ES6, and ES8 conditions, across approximately 4 weeks.
Peak heart rate expressed as a percentage of age-predicted maximum heart rate, calculated using the Tanaka equation: 208 - 0.7 × age (years).
Exercise Enjoyment Score
Time frame: Each prescribed exercise session on Days 1-2 of the ES4, ES6, and ES8 conditions, across approximately 4 weeks.
Self-reported enjoyment after each exercise snack on a numerical scale from 0 (not enjoyable at all) to 10 (extremely enjoyable). Higher scores indicate greater enjoyment.
Muscle Soreness Score
Time frame: Each prescribed exercise session on Days 1-2 of the ES4, ES6, and ES8 conditions, across approximately 4 weeks.
Self-reported muscle soreness after each exercise snack on a 4-level scale: 0 = none, 1 = mild, 2 = moderate, and 3 = severe.
Interval Between Consecutive Exercise Snacks
Time frame: Days 1-2 of the ES4, ES6, and ES8 conditions, across approximately 4 weeks.
Elapsed time in minutes between consecutive completed exercise snack sessions within each exercise condition, derived from recorded completion times.
Number of Exercise Interval Rule Violations
Time frame: Days 1-2 of the ES4, ES6, and ES8 conditions, across approximately 4 weeks.
Number of occasions on which consecutive exercise snack sessions were separated by less than the prescribed minimum interval of 60 minutes.
Daily Step Count
Time frame: Days 1-2 of each of the four experimental conditions (approximately 4 weeks in total).
Mean daily step count measured using a waist-worn ActiGraph wGT3X-BT accelerometer during each experimental condition.
Daily Sedentary Time
Time frame: Days 1-2 of each of the four experimental conditions (approximately 4 weeks in total).
Daily sedentary time (minutes per day) measured by accelerometry, using fewer than 100 vertical-axis counts per minute to identify sedentary behavior.
Non-Intervention Moderate-to-Vigorous Physical Activity
Time frame: Days 1-2 of each of the four experimental conditions (approximately 4 weeks in total).
Daily minutes of moderate-to-vigorous physical activity (MVPA) measured by accelerometry, excluding activity recorded from 1 minute before to 1 minute after each prescribed exercise snack.
Number of Symptomatic Hypoglycemic Events
Time frame: From baseline assessment through the final adverse-event follow-up after the fourth condition (approximately 5 weeks per participant).
Number of symptomatic hypoglycemia episodes confirmed by capillary blood glucose measurements below 3.9 mmol/L. Symptoms included palpitations, sweating, hunger, or dizziness.
Number of CGM-Detected Hypoglycemic Events Below 3.9 mmol/L
Time frame: Days 1-2 of each of the four experimental conditions (approximately 4 weeks in total).
Number of CGM-derived hypoglycemic events defined as sensor glucose below 3.9 mmol/L continuously for at least 15 minutes.
Number of CGM-Detected Level 2 Hypoglycemic Events
Time frame: Days 1-2 of each of the four experimental conditions (approximately 4 weeks in total).
Number of CGM-derived level 2 hypoglycemic events defined as sensor glucose below 3.0 mmol/L continuously for at least 15 minutes.
Number of Adverse Events
Time frame: From baseline assessment through the final adverse-event follow-up after the fourth condition (approximately 5 weeks per participant).
Number of adverse medical events recorded during the study, regardless of relationship to the intervention, including musculoskeletal injury, cardiovascular symptoms, and other clinical events.
Number of Serious Adverse Events
Time frame: From baseline assessment through the final adverse-event follow-up after the fourth condition (approximately 5 weeks per participant).
Number of serious adverse events recorded during the study, including events resulting in death, life-threatening conditions, hospitalization or prolonged hospitalization, or major disability.
Other measures
Relative Support for Candidate Exercise Dose-Response Models
Time frame: Days 1-2 of each of the four experimental conditions (approximately 4 weeks in total).
Akaike weights derived from comparisons of seven prespecified dose-response models: linear, log-linear, quadratic, threshold, Emax, unimodal with a peak at six sessions per day, and fully categorical. Weights represent relative model support in the specified candidate set.
Change in Sensor Glucose 60 Minutes After Individual Exercise Snacks
Time frame: From 30 minutes before to 120 minutes after each exercise snack during Days 1-2 of ES4, ES6, and ES8 conditions.
Change in CGM sensor glucose (mmol/L) from the exercise completion time (0 minutes) to 60 minutes afterward, separately for postprandial and non-postprandial exercise windows. Glucose trajectories from -30 to +120 minutes were examined, with corresponding clock-time readings from the control condition used as a reference.
Review the complete result tables and limitations in the official record.
Open official results ↗Research locations (1)
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1 locations
Capital University of Physical Education and SportsBeijing, Beijing Municipality, ChinaStatus unknown
Study team and timeline
- Lead sponsor
- Capital University of Physical Education and Sports, China
- Study start
- Sep 1, 2025 Actual
- Primary completion
- Oct 6, 2025 Actual
- Study completion
- Jul 1, 2026 Actual
- First posted
- Nov 10, 2026 Actual
- Last updated
- Nov 10, 2026 Actual
Official study contacts
No central contact is listed. Check the locations and the official record.
Official study title
Effects of 1-Min Exercise Snacks on Daytime Glucose in Adults With Type 2 Diabetes Not Treated With Insulin: A Randomized Crossover Trial
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Source: ClinicalTrials.gov API v2. Information is submitted by sponsors and investigators. NLM does not approve the safety or science of all listed studies. Registry disclaimer.
Retrieved: Nov 12, 2026 · Last registry update: Nov 10, 2026
