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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04320446
Other study ID # Nº 507/CEIH/2018
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 1, 2019
Est. completion date November 30, 2019

Study information

Verified date March 2020
Source Universidad de Granada
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Maximal fat oxidation during exercise (MFO) and the intensity of exercise that elicits MFO (Fatmax) has been recognized as potential determinants of endurance performance.

The purpose of this study was to determine the possible interaction between the effects of diurnal variation (morning vs. afternoon) and caffeine ingestion on MFO, Fatmax and VO2 max in endurance-trained men. Specifically, the investigators sought to elucidate whether the stimulant actions of caffeine could reverse the decrements of MFO and Fatmax observed in the morning.


Description:

Body weight, height, body composition (DXA), exercise test (MFO and VO2max assessment) will be measured during the 4 evaluations.

Participants were randomized into 4 exercise test conditions:

1. Exercise test in the morning with placebo intake

2. Exercise test in the evening with placebo intake

3. Exercise test in the morning with caffeine intake

4. Execrise test in the evening with caffeine intake


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date November 30, 2019
Est. primary completion date November 30, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Having a body mass index (BMI) ranged from 18.5 to 28 kg/m2

- not suffering any specific disease which can be aggravated by physical exercise

- having previous experience in endurance training (i.e. self-reporting at least 2 years of cycling or running training including more than 3 training sessions/week).

- Participant must be capable and willing to provide consent, understand exclusion criteria, instructions and protocols.

Exclusion Criteria:

- Being smoker

- Taking medication or drugs

- Any non-controlled medical condition which could influence results or could be worsened by the participation in the study

- Are deemed unsuitable by the investigator for any other reason, that prevent data collection.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Test in the morning
The exercise test was performed between 8 a.m and 11 a.m
Test in the afternoon
The exercise test was performed between 5 p.m. and 8 p.m.a

Locations

Country Name City State
Spain Instituto Mixto Universitario Deporte Salud Granada

Sponsors (1)

Lead Sponsor Collaborator
Universidad de Granada

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary MFO Maximal fat oxidation during exercise Through study completion, an average of 1 month
Secondary FATmax The intensity of exercise that elicits MFO Through study completion, an average of 1 month
Secondary VO2max Cardiorrespiratory fitness measured by maximal oxygen uptake Through study completion, an average of 1 month
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