NCT02203539

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
74

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jul 2014

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 16, 2014

Completed
3 months until next milestone

Study Start

First participant enrolled

July 1, 2014

Completed
29 days until next milestone

First Posted

Study publicly available on registry

July 30, 2014

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2015

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2015

Completed
Last Updated

July 2, 2015

Status Verified

July 1, 2015

Enrollment Period

10 months

First QC Date

April 16, 2014

Last Update Submit

July 1, 2015

Conditions

Keywords

circadian rhythmlight exposureexercise capacityendurancestrengthreaction

Outcome Measures

Primary Outcomes (1)

  • 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.

Secondary Outcomes (2)

  • Reaction time in milliseconds (ms)

    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.

  • Maximum handgrip strength in kilo gramm (kg)

    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.

Study Arms (3)

bright light

EXPERIMENTAL

Intervention: exposure to bright light

Other: exposure to bright light

blue-enriched light

EXPERIMENTAL

Intervention: exposure to blue-enriched light

Other: exposure to blue-enriched light

normal light

EXPERIMENTAL

Intervention: exposure to normal light

Other: exposure to normal light

Interventions

exposure for 60 minutes in duration

normal light

exposure to bright light for 60 minutes of duration

bright light

exposure to blue-enriched light for 60 minutes of duration

blue-enriched light

Eligibility Criteria

Age18 Years - 35 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • BMI 18 to 30 kg/m2
  • endurance performance \>= 55 ml/min/kg peak oxygen uptake

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department for Sport, Exercise and Health, Section Sports and Exercise Medicine, University of Basel

Basel, 4052, Switzerland

Location

Study Officials

  • Arno Schmidt-Trucksäss, Prof Dr

    Departement of Sports, Exercise and Health, University of Basel

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Prof Arno Schmidt-Trucksäss, MD, MA

Study Record Dates

First Submitted

April 16, 2014

First Posted

July 30, 2014

Study Start

July 1, 2014

Primary Completion

May 1, 2015

Study Completion

May 1, 2015

Last Updated

July 2, 2015

Record last verified: 2015-07

Locations