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An Exploratory Clinical Study on the Impact of Time-Restricted Feeding on Cardiac Function in Myocardial Infarction Patients During Recovery

An Exploratory Clinical Study on the Impact of Time-Restricted Feeding on Cardiac Function in Myocardial Infarction Patients During Recovery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113235
Enrollment
Unknown
Registered
2025-11-26
Start date
2025-11-27
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

Cardiac Dysfunction

Interventions

Time-Restricted Feeding Group:Participants in the Time-Restricted Eating (TRE) group will be required to consume all daily food within a self-selected 8-hour window, such as 8:00-16:00, 9:00-17:00, or
Regular Diet Group:The Normal Diet Group will maintain their regular eating pattern.

Sponsors

Tai'an Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1 Age 25-70 years; 2 Patients with myocardial infarction (with or without stent placement) within 1 month of onset. Diagnosis of myocardial infarction shall be based on symptoms, electrocardiogram, myocardial enzyme profiles, and imaging findings. Cardiac function classification shall follow NYHA criteria, while systolic and diastolic function shall be assessed through cardiac color Doppler ultrasound combined with serological test data; 3 Presence of systolic and/or diastolic dysfunction; 4 Voluntary participation in the trial with signed informed consent.

Exclusion criteria

Exclusion criteria: 1 Patients with severe chronic diseases such as diabetes, malignant tumors, hepatic or renal insufficiency, depression, hyperthyroidism, infectious diseases, etc; 2 Pregnant or lactating women; heavy smokers or individuals with alcohol abuse; 3 Those with poor compliance or inability to cooperate with examinations, thereby compromising clinical research integrity.

Design outcomes

Primary

MeasureTime frame
Left ventricular ejection fraction by echocardiography(LVEF);Results of the Six-Minute Walk Test;NT-proBNP;Left atrial volume index by echocardiography;Electrocardiogram (ECG);

Secondary

MeasureTime frame
Troponin I;Soluble ST-2;blood pressure;

Countries

China

Contacts

Public ContactSuJing

Tai'an Central Hospital

sujing0538@126.com+86 187 0538 1077

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026