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Clinical Trials in China / NCT07693049
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Cardiopulmonary Exercise Testing-based High-intensity Interval Training For Improving Heart Failure With Preserved Ejection Fraction

NCT07693049 · tracked via the Priya Life Science China tracker
Sponsor
Peking University Third Hospital
Phase
Not applicable
Started
2026-07
Last updated
2026-07-14

Condition(s) studied

HFpEF - Heart Failure With Preserved Ejection Fraction

Investigational drug(s) / intervention(s)

High-intensity interval training

High-intensity interval training: Subjects in the intervention group will receive a personalized high-intensity interval training (HIIT) protocol based on cardiopulmonary exercise testing (CPET) and will undergo a 24-week HIIT intervention, four times per week.The exercise protocol consisted of a 5-minute warm-up at 30-40 watts, followed by 8 cycles of high-intensity exercise performed at 80-90% of peak VO₂ for 30 seconds, each interspersed with a 60-second active recovery period of low-intensity exercise at 50-60% of peak VO₂ , and concluded with a 5-minute cool-down at 30-40 watts.

Study summary

Cardiovascular-Kidney-Metabolic (CKM) Syndrome is a continuous clinical disease spectrum integrating cardiovascular, renal, and metabolic disorders. Heart failure with preserved ejection fraction (HFpEF) is considered Stage 4 of CKM syndrome, characterized primarily by impairment of cardiac structure and function. Numerous studies have confirmed that exercise intervention is effective in improving metabolic profiles and inflammatory status in Stages 0-3 of CKM syndrome (e.g., obesity, metabolic syndrome, hypertension, and diabetes), and significantly improves clinical outcomes. However, for Stage 4 CKM syndrome, especially in patients with HFpEF, conventional exercise prescription faces significant challenges in balancing safety and efficacy. Moreover, traditional "one-size-fits-all" exercise rehabilitation strategies have failed to significantly improve clinical outcomes due to the lack of individualized precision approaches.

To address this gap, this study proposes to adopt a multicenter, randomized, controlled design, enrolling patients with HFpEF at Stage 4 of CKM syndrome and randomly assigning them to either a personalized high-intensity interval training (HIIT) intervention group or a standard care control group. The \*\*primary endpoint\*\* of this study is the change in peak oxygen consumption (peak VO₂) from baseline after 24 weeks of intervention. In addition, a series of \*\*secondary endpoints\*\* have been established for comprehensive evaluation, including inflammatory biomarkers, cardiac structure and function, quality of life, and composite clinical events. These endpoints aim to comprehensively assess the intervention effects from the perspectives of cardiopulmonary function, metabolism and inflammation, quality of life, and clinical outcomes, as well as to explore the underlying mechanisms.

This study is expected to validate the beneficial effects of personalized exercise on peak VO₂ and various secondary endpoints in patients with Stage 4 CKM syndrome. It will not only provide high-level evidence-based support for exercise therapy in HFpEF but also deepen the understanding of the role of exercise intervention in the full-course management of CKM syndrome, offering key scientific support for the development of precision prevention and treatment strategies across all stages.

Eligibility

Sex
ALL
Min age
35 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: 1. Men and women aged 35-70 years; 2. Physical inactivity / sedentary lifestyle defined as: Sedentary behavior: average daily sitting time \> 6 hours over the past 6 months; AND/OR Insufficient physical activity: average weekly moderate-intensity physical activity \< 150 minutes or vigorous-intensity physical activity \< 75 minutes as assessed by the International Physical Activity Questionnaire (IPAQ); 3. Patients with HFpEF at Stage 4 of CKM syndrome who have been clinically stable within the past month (New York Heart Association \[NYHA\] functional class II-III); 4. Willingness to improve health status through appropriate exercise. Exclusion Criteria: 1. Presence of contraindications to cardiopulmonary exercise testing (CPET); 2. Positive findings on the exercise electrocardiogram (ECG) during CPET; 3. Diagnosis of psychiatric disorders; 4. Presence of movement disorders or lower extremity exercise-related injuries within the past 6 months; 5. Women who are pregnant, breastfeeding, or planning to become pregnant in the near future; 6. Other conditions deemed unsuitable for participation in this study by the investigators; 7. Refusal to sign the informed consent form.

Primary outcome measure(s)

Trial sites (12)

FacilityCityRegionStatus
Beijing Chao-Yang Hospital, Capital Medical University Beijing China
Beijing Hospital Beijing China
Beijing Xiaotangshan Hospital Beijing China
Beijing Zhongguancun Hospital Beijing China
Community Health Station of the Party School of the Central Committee of C.P.C Beijing China
Jimenli Community Health Service Center Beijing China
Peking University First Hospital Beijing China
Peking University People's Hospital Beijing China
Peking University Third Hospital Beijing China
Xueyuanlu Community Health Service Center Beijing China
Shanghai East Hospital Shanghai China
Wuhan Asia Heart Hospital Wuhan China

More Peking University Third Hospital trials in China

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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 NCT07693049 on ClinicalTrials.gov ↗ ← All trials in China