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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02297646
Other study ID # Saarland University - CHO
Secondary ID
Status Completed
Phase Phase 0
First received September 10, 2013
Last updated November 20, 2014
Start date August 2012
Est. completion date December 2013

Study information

Verified date November 2014
Source Saarland University
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate the effects of carbohydrate intake on training efficacy and health parameters of an endurance training program in healthy adults.


Description:

Carbohydrate availability in endurance exercise seems to attenuate exercise-induced perturbations of cellular homeostasis and consequently diminishes the stimulus for training adaptation. Therefore, a negative relationship with exercise efficacy seems plausible. However, experimental evidence is rare and far from conclusive. Therefore, the present study aims to test the influence of carbohydrate intake on the efficacy of a typical preventive training program.


Recruitment information / eligibility

Status Completed
Enrollment 23
Est. completion date December 2013
Est. primary completion date December 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 30 Years to 65 Years
Eligibility Inclusion Criteria:

- no diseases

- nonsmoker

- BMI 25-30 kg/m²

- blood pressure <160/100 mm/Hg

- unmedicated

- untrained status

- V?O2max < 50 mL/kg/min

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms

  • Health Status
  • Maximal and Submaximal Parameters of Physical Performance

Intervention

Behavioral:
Endurance Training


Locations

Country Name City State
Germany Institute of Sports and Preventive Medicine, Saarland University Saarbrücken Saarland

Sponsors (1)

Lead Sponsor Collaborator
Saarland University

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Maximum oxygen consumption (VO2max) VO2max 24 weeks No
Secondary Numerous serum parameters from venous blood (LDL, HDL, Cholesterol, Triglycerides) cardiovascular parameters:
LDL
HDL
Cholesterol
Triglycerides
24 weeks No
Secondary Resting heart rate 24 weeks No
Secondary Resting blood pressure 24 weeks No
Secondary Body fat (Skinfold thickness) Skinfold thickness 24 weeks No
Secondary Ventilatory anaerobic threshold (VT) VT 24 weeks No
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