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Functional Food Application of Okara Protein Hydrolysate (OPH)- for Anti-exercise-fatigue

Functional Food Application of Okara Protein Hydrolysate (OPH)- for Anti-exercise-fatigue

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05000918
Enrollment
18
Registered
2021-08-11
Start date
2020-07-17
Completion date
2020-10-31
Last updated
2021-08-11

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

Conditions

Healthy

Brief summary

The aim of this study is to investigate the anti-exercise-fatigue effects of okara protein hydrolysate (OPH) in men

Detailed description

Each subject must undergo a cardiopulmonary capacity test to assess the maximum oxygen uptake 1 week before the intervention (day 1), and then eat the test food for 4 weeks (day 8 to day 35). Before and after the intervention (the 8th and 35th day), posture measurement, diet questionnaire survey and endurance exercise ability test were carried out. The trial period was 35 days. The subjects will take blood samples before, during, after, and 30 minutes and 60 minutes after the end of the two endurance exercise tests. During the whole period of participating in the program, blood will be collected 10 times, each with a blood volume of 15 mL. Gas is collected during the period and within 1 hour after exercise. Gas is collected every 15 minutes and 1 minute at a time. Analyze his exercise time, oxygen intake and blood biochemical value.

Interventions

DIETARY_SUPPLEMENTOkara protein hydrolysate (OPH)

Okara protein hydrolysate (OPH) was a pack of dried beige powder. It can be stored at room temperature, but it must be exposed to direct sunlight.

Sponsors

National Taichung University of Education
CollaboratorUNKNOWN
Chung Shan Medical University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
20 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* The subject is a male and aged 20-40. * The subject has a usual exercise habit (exercising 2 times or more per week) and did not participate in professional sports competitions or professional sports training during the study period. * No smoking or drinking habits. * No food allergies and the liver function is normal. * No cardiovascular diseases or other chronic diseases, and no serious illnesses requiring hospitalization during the study period. * The subject can understand the test process described in the consent form and the possible potential risks and benefits, and can sign the consent form. * The subject can accept dietary control during the trial period.

Exclusion criteria

* Those who have taken nutritional supplements containing branched-chain amino acids. * Those who cannot complete the endurance exercise ability test. * Those who are diagnosed with kidney disease, heart disease, or cancer and are still under active treatment. * Have used other drugs, whose pharmacological effects may affect fatigue. * Subjects who have systemic infections and require systemic antibiotics.

Design outcomes

Primary

MeasureTime frameDescription
Change the metabolic substances level after intervention8th day, 35th dayCompare the difference of blood lactate, lactate dehydrogenase, and creatine kinase level after exercise between pre- and post-intervention

Secondary

MeasureTime frameDescription
Change the exercise time after intervention8th day, 35th dayCompare the exercise time between pre- and post-intervention

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026