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Effects of High Intensity Training Combined with Sodium Bicarbonate Supplementation on Skin Condition in Healthy Individuals

Effects of High Intensity Training Combined with Sodium Bicarbonate Supplementation on Skin Condition in Healthy Individuals

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101272
Enrollment
Unknown
Registered
2025-04-23
Start date
2025-04-30
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Skin diseases

Interventions

Control group:Control solvent+high intensity training
Experiment group:Sodium Bicarbonate+high intensity training

Sponsors

Xiangtan First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: (1) Basic inclusion conditions Demographic indicators Age: 18~40 years old (including boundary value) Gender: unlimited (gender distribution needs to be recorded, and the final enrollment needs to meet the sex ratio of 1:1 between the experimental group and the control group) BMI index: 18.5= male, 120 g/L>= female White blood cell count: (4~10)×10?/L Fasting blood glucose: 3.9~6.1 mmol/L Four blood lipids: Total cholesterol =50th percentile value for age and sex No abnormal ST segment changes in exercise stress test (Bruce protocol assessment) Baseline test of physical fitness 1 minute push-up >= 20 times for men and 12 times for women Seated forward bend >= +10 cm (5) Other access requirements Legal and cognitive requirements Persons with full capacity for civil conduct who hold valid identity certificates; Pre-authorization informed consent process: Read the informed consent form completely and sign it independently> designated agent reads the informed consent form and signs it independently> designated agent reads and signs the informed consent form If there is a designated agent, the designated agent needs to sign the informed consent form together with the agent's relevant documents. Study Adherence: Commitment to continuous participation in the training program (attendance>=85%) Agree to comply with the dietary management of the study side (>= 20 hours per day)

Exclusion criteria

Exclusion criteria: If any of the following criteria is met, subjects cannot be enrolled in this interventional study: (1) Participated in any interventional clinical study (including drug and instrument biologics trials) within 3 months before enrollment; (2) History of major systemic diseases (need to meet the current clinical significance), the details are as follows: Circulatory system diseases (such as coronary heart disease, hypertension level II or above, severe arrhythmia), metabolic endocrine diseases (diabetes, hypothyroidism, etc.), urinary system diseases (chronic kidney disease stage 3 and above), neurological diseases (epilepsy, stroke sequelae, etc.), immune system abnormalities (primary acquired immune deficiency, autoimmune diseases), other system diseases (hematologic system, respiratory system, mental diseases, etc.); (3) Renal function limitation requirements (serum creatinine needs to be standardized detection methods) CockcroftGault formula calculates creatinine clearance (CrCl) <80mLémin; CrCl = [(140 age) × weight (kg)] / [0.814 × Scr(µmol/L)] (4) Clinical examination abnormalities, any of the following clinically significant abnormalities (researchers judged): abnormal signs of physical examination, pathological changes in ECG, laboratory test values ??exceeding the normal range by more than 20%, significant abnormalities in ultrasound radiation imaging, and continuous deviations from the baseline value; (5) Other situations that are not suitable for selection: After comprehensive evaluation by the research team, there are special circumstances that affect the integrity of the study or the safety of the subjects.

Design outcomes

Primary

MeasureTime frame
Skin condition assessment;

Secondary

MeasureTime frame
Blood routine;Blood biochemistry;Blood high-throughput sequencing;Serum inflammatory factor ;Magnetic resonance examination;

Countries

China

Contacts

Public ContactGenqing Xie

The first people's hospital of Xiangtan hospital

genqingxie@qq.com+86 181 6360 2595

Outcome results

None listed

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