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Clinical Trials in China / NCT07769840
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Rowing and Cycling Reduce Inflammation in Early-Stage Type 2 Diabetes

NCT07769840 · tracked via the Priya Life Science China tracker
Sponsor
The 95th Hospital of Putian,Putian, Fujian, China
Phase
Not applicable
Started
2026-10-01
Last updated
2026-08-18

Condition(s) studied

Diabetes

Investigational drug(s) / intervention(s)

Continuous Exercise - Cycling GroupRowing Ergometer High-Intensity Interval TrainingCombined Training Standard

Continuous Exercise - Cycling Group: Warm-up: 5 minutes of low-intensity cycling (50-60 W, approximately 40%-50% HRmax of continuous power cycling at) Main Training: 40 minutes 65%-75% HRmax (approximately 60%-70% VO₂peak), maintaining a cadence of 60-80 rpm Cool-down: 5 minutes of low-intensity cycling followed by stretching Total Duration: 50 minutes

Rowing Ergometer High-Intensity Interval Training: Warm-up: 5 minutes of low-intensity rowing at approximately 50% of maximum heart rate (HRmax). Main Training: 24 minutes of interval training consisting of 4 sets of high-intensity rowing for 4 minutes each (85%-90% HRmax), with 2 minutes of low-intensity active recovery (50%-60% HRmax) between each set. Maintain a stroke rate of 24-30 strokes per minute (SPM) for high-intensity intervals and 18-22 SPM for recovery intervals. Cool-down: 5 minutes of low-intensity rowing combined with stretching. Total Duration: 34 minutes

Combined Training Standard: Warm-up: 5 minutes of low-intensity activity (choose either cycling or rowing). Rowing Machine Segment: 20 minutes at an intensity of 65%-75% of maximum heart rate (HRmax) (approximately 60%-70% of VO₂peak), with a stroke rate of 22-26 strokes per minute (SPM). Bicycle Segment: 20 minutes at an intensity of 65%-75% of HRmax (approximately 60%-70% of VO₂peak), with a cadence of 60-80 revolutions per minute (rpm). Cool-down: 5 minutes of stretching. Total Duration: 50 minutes

Study summary

This multicenter randomized controlled trial evaluates the short-term (7-day) effects of different rowing-cycling exercise regimens on postprandial glycemic excursions in newly diagnosed type 2 diabetes patients (aged 18-60 years, diagnosis ≤12 months, drug-naïve). A total of 120 participants will be randomized into five groups: control, moderate-intensity continuous cycling, high-intensity interval rowing, and standard combined exercise (rowing + cycling, 50 min). The primary outcome is inflammatory cytokines (IL-6, TNF-α, IL-1β, IL-1ra, IL-10, hs-CRP), body Composition and functional Indicators. Secondary outcomes include change in continuous glucose monitoring-derived glycemic variability (CONGA), and time-in-range. Mixed-effects models will quantify dose-response relationships and identify key effect modifiers (e.g., age). This study aims to establish an evidence-based precision exercise prescription for early-stage type 2 diabetes management.

Eligibility

Sex
ALL
Min age
18 Years
Max age
60 Years
Healthy volunteers
No
Inclusion Criteria: 1. Age between 18-60 years, no gender limited; 2. Meeting the WHO 1999 diagnostic criteria for T2DM, with a diagnosis time ≤12 months; 3. Not having received hypoglycemic drug treatment (or only lifestyle intervention, and stopped medication ≥4 weeks before enrollment); 4. Fasting blood glucose 7.0-13.9 mmol/L, glycated hemoglobin (HbA1c) 6.5%-10.0%; 5. No regular exercise in the past 3 months (less than 2 times per week of moderate or higher intensity exercise, each \<30 minutes); 6. Voluntarily signing the informed consent form. Exclusion Criteria: 1. Type 1 diabetes, gestational diabetes, or other special types of diabetes; 2. Severe cardiovascular or cerebrovascular diseases (NYHA heart function ≥III, recent myocardial infarction or unstable angina); 3. Uncontrolled hypertension (resting systolic blood pressure ≥160 mmHg or diastolic blood pressure ≥100 mmHg); 4. Severe liver or kidney dysfunction (ALT/AST ≥3 times the upper limit of normal, or eGFR\<60 mL/min/1.73m²); 5. Severe diabetic complications (such as proliferative retinopathy, severe neuropathy, diabetic foot); 6. Pregnant or breastfeeding women; 7. Mental illness or cognitive impairment that prevents compliance with the study; 8. Stress events such as infection, trauma, or surgery in the past month; 9. Participation in other interventional clinical studies; 10. Musculoskeletal diseases of the upper or lower limbs that affect rowing machine or bicycle exercise.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The Ethics Committee of Putian 95 Hospital Putian Fujian

More The 95th Hospital of Putian,Putian, Fujian, China trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07769840 on ClinicalTrials.gov ↗ ← All trials in China