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Study on the effect of compound amino acid energy drink on alleviating sports fatigue

Study on the effect of compound amino acid energy drink on alleviating sports fatigue.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066249
Enrollment
Unknown
Registered
2022-11-29
Start date
2022-12-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

exercise fatigue

Interventions

Energy drink Group:compound amino acid energy drink(after 7 to 14 days washout,the placebo drink is given )
control group:placebo drink(after 7 to 14 days washout,the compound amino acid energy drink is given)

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Healthy youth, male or female; 18-35 years old; Maintain at least 1 year, >= 3 times/week, and carry out aerobic endurance exercise for more than 30 minutes each time.

Exclusion criteria

Exclusion criteria: 1) BMI>=28kg/m 2 2) Smokers; 3) Have participated in or are participating in other clinical trials within three months recently (the first time of taking the study product); 4) Those who often drink coffee or strong tea or functional drinks, the frequency of drinking is more than 3 times/week, and the caffeine intake each time is more than 200mg; 5) Those who are about to receive or are receiving drug treatment; 6) Patients with abnormal glucose tolerance, hyperglycemia or diabetes; 7) The maximum MET value of cardiopulmonary exercise test is less than 8.0; 8) Those with organic diseases such as heart, liver, kidney and blood system or those with chronic diseases; 9) Unable to perform physical function test and answer the questionnaire questions correctly; 10) Failure to follow the test procedure; 11) Those who are allergic to the tested product components; 12) Pregnant and lactating women; 13) Refusing to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
lactic acid;RPE;

Secondary

MeasureTime frame
Heart rate;blood pressure;Fatigue related hormone;Change of substance metabolism;

Countries

China

Contacts

Public ContactChang Cuiqing

Peking University Third Hospital

13521960678@163.com13521960678

Outcome results

None listed

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