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Sports nutrition intervention studies

Sports nutrition intervention studies

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076750
Enrollment
Unknown
Registered
2023-10-17
Start date
2023-03-02
Completion date
Unknown
Last updated
2023-10-22

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

Conditions

Healthy participants

Interventions

Intervention group 1:During the intervention period, the intervention group consumed meal replacement products three times a week in place of dinner and aerobic exercise three times a week for approxi
Control group 1:During the intervention period, the control group ate normally and aerobic exercise three times a week for approximately 40 minutes each time while maintaining their habitual exercise
Intervention group 2:During the intervention period, the intervention group exercised anaerobically 3 times per week for 40 minutes each time and took the intervention protein drink within 30 minutes
Control group 2:During the intervention period, the intervention group exercised anaerobically 3 times per week for 40 minutes each time and took the bottled water within 30 minutes after exercise.

Sponsors

Nankai University Medical School
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 34 Years

Inclusion criteria

Inclusion criteria: Product 1 was planned to recruit healthy women aged 18-35 years with BMI 24-28 kg/m2 or body fat =25% or waist-to-hip ratio =0.8 (20 in each group) and Product 2 was planned to recruit healthy men aged 18-35 years with BMI 18.5-23.9 kg/m2 and no anaerobic exercise habit (15 in each group).

Exclusion criteria

Exclusion criteria: Exclude participants who do not accept the flavor of the product, participants who are not willing to cooperate with fat loss diet or exercise, participants with diseases related to exercise, such as cardiovascular diseases, bone and joint diseases, chronic pain diseases, participants with gastrointestinal diseases, participants with abnormal thyroid function; participants who are taking other exercise supplements during the trial; participants with smoking and alcohol habits; and other participants who are considered unsuitable by PI to participate in the trial.

Design outcomes

Primary

MeasureTime frame
Body composition;Body circumference;

Secondary

MeasureTime frame
Blood parameters;Urine parameters;

Countries

China

Contacts

Public ContactDancai Fan

School of Medicine, Nankai University

fandancai@nankai.edu.cn+86 186 1304 3081

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 12, 2026