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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02203539
Other study ID # EKNZ 2014-056
Secondary ID
Status Completed
Phase N/A
First received April 16, 2014
Last updated July 1, 2015
Start date July 2014
Est. completion date May 2015

Study information

Verified date July 2015
Source University of Basel
Contact n/a
Is FDA regulated No
Health authority Switzerland: Ethikkommission
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine if an exposure to light in the evening has a positive influence on physical performance regarding endurance, strength and reaction time.


Recruitment information / eligibility

Status Completed
Enrollment 74
Est. completion date May 2015
Est. primary completion date May 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 35 Years
Eligibility Inclusion criteria:

- BMI 18 to 30 kg/m2

- endurance performance >= 55 ml/min/kg peak oxygen uptake

Exclusion criteria:

- cardiovascular disease

- renal dysfunction

- shiftworking

- travels over time zones in the last 4 weeks

- high blood pressure (systolic blood pressure >170mmHg, diastolic blood pressure >100mmHg)

- depression

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Other:
exposure to normal light
exposure for 60 minutes in duration
exposure to bright light
exposure to bright light for 60 minutes of duration
exposure to blue-enriched light
exposure to blue-enriched light for 60 minutes of duration

Locations

Country Name City State
Switzerland Department for Sport, Exercise and Health, Section Sports and Exercise Medicine, University of Basel Basel

Sponsors (1)

Lead Sponsor Collaborator
University of Basel

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Work performed in kilo Joule (kJ) during the time trial ergometer test adjusted for the VO2peak. Participants will perform one baseline test (ergometer ramp test) and seven days later a twelve minute lasting ergometer time trial test which starts 10 minutes after an exposure to light for 60minutes. The work performed in kilo Joule during the time trial ergometer test will be assesed at the end of the time trial and will be the main outcome measure and adjusted for the VO2peak meausred during the baseline test. The outcome measure will be assesed at the end of the 12minute time trial ergometer test. No
Secondary Reaction time in milliseconds (ms) Participants will perform one baseline reaction time task 20 to 15 minutes before the light exposure. 0 to 5 minutes after the 60 minutes lasting light exposure they will perform the reaction task again. The time in milliseconds from the reaction task after the light exposure will be the secondary outcome measure and adjusted for the baseline test before light exposure. Reaction time task will be performed at baseline (20 to 15 minutes before the light exposure) and 0 to minutes after the light exposure which will be the secondary outcome measure. No
Secondary Maximum handgrip strength in kilo gramm (kg) Participants will perform one baseline maximum hand grip strength test 15 to 10 minutes before the 60 minutes lasting light exposusre and perform a second test, which will be the outcome measure 5 to 10 minutes after the light exposure. The strength in kg will be adjusted for the strength in kg measured at baseline. Maximum handgrip strength will be tested at baseline (15 to 10 minutes before the light exposure) and 5 to 10 minutes after the 60 minutes lasting light exposure. No
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