Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05129917
Other study ID # TSMH No.13-023-A2
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 1, 2013
Est. completion date December 31, 2013

Study information

Verified date November 2021
Source TCI Co., Ltd.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The main purpose of the present study is to determine the effects of acute and short-term (14 days) ginseng combined with branch chained amino acids supplementation on endurance exercise performance and the ability of anti-fatigue. In addition, this study also measured the performance of continuous attention during recovery period to examine the effect of supplementation on central fatigue.


Description:

Muscle fatigue was a common problem after exercise. When fatigue occured, body functions were affected and changed. Changbai Mountain ginseng had higher anti-fatigue substances than general commercial ginseng. And recent studies had showed that the supplementation of branched chain amino acids (BCAA), including leucine, isoleucine and valine, can increase attention and reduce fatigue. However, its effect on Changbai Mountain ginseng combined with BCAA was still unclear. Subjects were allocated to Gojinsen® drinks and placebo group (1:1 ratio) for 14 days, and then examined by maximal oxygen consumption, time to exhaustion, rating of perceived exertion (RPE), oxygen saturation (SPO2) , blood lactate concentration, and continuous attention performance test (CPT II). The Gojinsen® group significant increased maximal oxygen consumption, time to exhaustion, and attention compared to placebo group. Moreover, the Gojinsen® group significant decreased lactate concentration and fatigue compared to placebo group. By this study, Gojinsen® drinks did not showed absolute anti-fatigue effect but provided the objective evidence of fatigue-related measurement and the therapeutic potential for people suffering from exercise fatigue.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date December 31, 2013
Est. primary completion date December 1, 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 25 Years
Eligibility Inclusion Criteria: 1. healthy male and female adults aged 20-25 years old . 2. without heart, liver, kidney, endocrine or other major organic diseases). 3. had at least 3 months experience in performing exercise Exclusion Criteria: 1. BMI of the study subjects must be less than 25.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Placebo
consume 1 sachet per day for 14 day
Gojinsen® drinks
consume 1 sachet per day for 14 day

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
TCI Co., Ltd.

Outcome

Type Measure Description Time frame Safety issue
Primary Endurance exercise performance testing the subjects arrived to the laboratory and wore the oxygen uptake mask of energy metabolism analyzer (Sensor Medics, Vmax29, USA) to measure the subjects' oxygen uptake Execution on the 14th day
Primary rating of perceived exertion The Rated Perceived Exertion was measured during the treadmill exercise by Bruce Protocol, a gradual increase in the speed and the slope of the treadmill every 3 minutes. Execution on the 14th day
Primary blood lactate fingertip capillary blood was placed in automated blood lactate analyzer Execution on the 14th day
Primary Continuous attention performance test 10 minutes after maximal exercise test, the subjects performed attention tests that used Canon continuous attention software Execution on the 14th day
See also
  Status Clinical Trial Phase
Completed NCT01515033 - Aerobic Exercise on PETCO2 Response in Coronary Artery Disease Patients Phase 2
Completed NCT06061237 - Effects of Aerobic Thai Dance in Patient With Diabetic Peripheral Neuropathy N/A
Completed NCT03986840 - Multicomponent Exercise Training in Frail Elderly N/A
Completed NCT03082781 - Dietary Choice in Active Older Adult Women N/A
Completed NCT03007459 - The Health of Competitive Fitness Athletes
Completed NCT04135729 - Mental Health in Fitness Instructors
Not yet recruiting NCT05241925 - Effects of Continuous and Interval Physical Training Through the Intensity of the Incremental Shuttle Walk Test, on Functional Capacity and Quality of Life in Women With Malignant Breast Cancer During Chemotherapy Treatment N/A
Terminated NCT05429307 - Turkish Adaptation, Validity and Reliability of Exercise Sensitivity Questionnaire
Active, not recruiting NCT05410899 - Exercise and Pelvic Floor Health Education Program Effectiveness
Completed NCT04220541 - Investigation of the Effects of Exercise on Patients With Chiari Malformation N/A
Completed NCT04010981 - Comparison of the Effectiveness of Virtual Reality and Video Assisted Exercises in Pediatric Chronic Kidney Disease. N/A
Recruiting NCT01783210 - Pregnancy Complications in Women With BMI>25 kg/m2 Enrolled in a Healthy Lifestyle and Eating Habits Program N/A
Not yet recruiting NCT06424743 - Preference of Women With Fibromyalgia Undergoing a Three Different Volumes of Resistance Training N/A
Recruiting NCT02768818 - Modulation of the Intestinal Flora With the Probiotic VIVOMIXX™ in Pregnant Women at Risk of Metabolic Complications Phase 3
Active, not recruiting NCT02766426 - Cytokine and Body Composition's Changes in Overweight/Obese Women N/A
Completed NCT06244030 - The Effect of Core Stabilization Exercises in Female Wrestlers N/A
Not yet recruiting NCT04940702 - Effectiveness of Focal Vibration and Blood Flow Restriction Within a Multicomponent Exercise Programme. N/A
Active, not recruiting NCT03005990 - The Effects of Exercise Training in Community-dwelling Elderly With Sleep Disturbances With Follow-up N/A
Completed NCT02106533 - Aerobic Exercise on Ventilatory Efficiency in CAD Patients Phase 2
Completed NCT01320904 - Exercise and Muscle Stimulation in Patients With Knee Osteoarthritis N/A