Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03062527
Other study ID # ULS00001
Secondary ID
Status Completed
Phase N/A
First received February 14, 2017
Last updated February 20, 2017
Start date January 2015
Est. completion date May 1, 2015

Study information

Verified date February 2017
Source Poznan University of Life Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the present study was to assess the influence of low vs moderate glycemic index of a 3-week diet on aerobic capacity, endurance performance and body mass and composition in endurance-trained athletes in a randomized, controlled crossover trial.


Description:

The effect of glycemic index of pre-exercise meal on endurance capacity and performance has been widely investigated. However, little is known about the adaptations to longer dietary interventions with different glycemic index and their influence on aerobic capacity and body composition in runners. Therefore, the purpose of this study was the assessment of the influence of low GI vs moderate GI of a 3-week diet on aerobic capacity, endurance performance and body mass and composition in endurance-trained athletes in a randomised, controlled crossover trial.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date May 1, 2015
Est. primary completion date February 6, 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 17 Years to 37 Years
Eligibility Inclusion Criteria:

- written consent to participate,

- male and female,

- a current medical clearance to practice sports,

- training experience: at least 3 years,

- minimum of 4 workout sessions a week lasting at least 1.5-2 hours/day,

- age: 17 - 37 years.

Exclusion Criteria:

- current injury,

- any health-related contraindication,

- declared general feeling of being unwell,

- unwilling to follow the study protocol,

- smoking, illicit drug use, alcohol consumption greater than 1-2 drinks/week, dietary supplements use less than 3 weeks before the study,

- females- being pregnant or planning to become pregnant during the study.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Dietary Intervention: Low vs. moderate glycemic index


Locations

Country Name City State
Poland Poznan University of Life Sciences, ul.Wojska Polskiego 31 Poznan Wielkopolska

Sponsors (1)

Lead Sponsor Collaborator
Poznan University of Life Sciences

Country where clinical trial is conducted

Poland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in aerobic capacity following low glycemic index diet Baseline and after 3 weeks
Primary Changes in aerobic capacity following moderate glycemic index diet Baseline and after 3 weeks
Primary Changes in performance in 12-min running test following low glycemic index diet Baseline and after 3 weeks
Primary Changes in performance in 12-min running test following moderate glycemic index diet Baseline and after 3 weeks
Primary Changes in fat mass and fat free mass following low glycemic index diet Fat mass (kg) and fat free mass (kg) analysis Baseline and after 3 weeks
Primary Changes in fat mass and fat free mass following moderate glycemic index diet Fat mass (kg) and fat free mass (kg) analysis Baseline and after 3 weeks
Secondary Statistical evaluation of the significance of differences between the changes in aerobic capacity indices 1 year
Secondary Statistical evaluation of the significance of differences between the changes in performance in 12-min running test 1 year
Secondary Statistical evaluation of the significance of differences between the changes in fat mass and fat free mass Fat mass (kg) and fat free mass (kg) 1 year
See also
  Status Clinical Trial Phase
Not yet recruiting NCT05934318 - L-ArGinine to pRevent advErse prEgnancy Outcomes (AGREE) N/A
Recruiting NCT05867433 - Strong Teens for Healthy Schools Change Club: A Civic Engagement Approach to Improving Physical Activity and Healthy Eating Environments N/A
Completed NCT02376530 - Price Changes and Nutrient Profiling Among Adult Grocery Shoppers N/A
Completed NCT01040975 - Teen CHAT: Improving Physician Communication With Adolescents About Healthy Weight N/A
Completed NCT00957814 - Nutritional Orientations and Adherence, Nutritional Status, Clinical and Life Quality Parameters of Heart Failure (HF) Patients N/A
Completed NCT00808756 - Study on Fermentable Carbohydrates in Healthy Infants N/A
Completed NCT03290118 - The Efficacy of Front-of-package Labelling Schemes: an Experimental Study N/A
Completed NCT03575884 - Fit 5 Kids Screen Time Reduction Curriculum for Latino Preschoolers N/A
Completed NCT03963778 - Organisational Culture and Nutritional Care
Completed NCT05633251 - Using Reinforcement Schedules to Increase Fruit&Vegetable Intake, Reduce Waste, and Increase School Lunch Participation N/A
Recruiting NCT05977959 - Optimizing the Impact of the Healthy School Recognized Campus Program on Youth's CVD Risk Factors N/A
Recruiting NCT05138276 - Effect of Autologous Cord Blood Mononuclear Cells for Digestive System in Preterm Neonates Early Phase 1
Completed NCT03906851 - Active and Healthy Kids in Telemark - a School Based Health Promoting Intervention N/A
Not yet recruiting NCT02950779 - Assessment of Handgrip Strength in Adults With Inflammatory Bowel Disease N/A
Completed NCT02486588 - Increasing Engagement With a Healthy Food Benefit N/A
Withdrawn NCT01184027 - Impact of Nutrition and Swallowing Function of Head and Neck Cancer Patients During the Course of Treatment N/A
Completed NCT01178398 - Understanding Fish Consumption Habits During Pregnancy N/A
Completed NCT01249508 - Nutrition Labeling Program to Promote Healthy Dietary Patterns N/A
Terminated NCT00577499 - Effect of Lubiprostone on Nutritional Status and Pulmonary Function in Adults With Cystic Fibrosis N/A
Completed NCT00109551 - Community Trial of Zinc Supplementation on Preschool Child Mortality and Morbidity in Southern Nepal Phase 3