NCT04745312

Brief Summary

The aim of the study is to examine the efficacy of supplementing sub-optimal ambient room lighting with a task lamp on working memory and procedural learning.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
16

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2021

Geographic Reach
1 country

1 active site

Status
unknown

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

February 4, 2021

Completed
5 days until next milestone

First Posted

Study publicly available on registry

February 9, 2021

Completed
20 days until next milestone

Study Start

First participant enrolled

March 1, 2021

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2022

Completed
Last Updated

February 18, 2022

Status Verified

February 1, 2022

Enrollment Period

1 year

First QC Date

February 4, 2021

Last Update Submit

February 16, 2022

Conditions

Keywords

LightCognitionAlertnessLearning

Outcome Measures

Primary Outcomes (1)

  • Working memory

    Percent correct responses on a 2-minute mental arithmetic task

    8 hour light exposure

Secondary Outcomes (1)

  • Procedural learning

    8 hour light exposure

Other Outcomes (5)

  • Vigilance

    8 hour light exposure

  • Subjective sleepiness

    8 hour light exposure

  • Memory recall

    8 hour light exposure

  • +2 more other outcomes

Study Arms (2)

Ambient light

ACTIVE COMPARATOR

Fluorescent ambient lighting

Device: Visible light

Ambient light plus task lamp

EXPERIMENTAL

Fluorescent ambient lighting plus task lamp

Device: Visible light

Interventions

Ambient room lighting will be supplemented with additional light from a task lamp.

Ambient lightAmbient light plus task lamp

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Aged between 18-30 years;
  • Healthy (no medical, psychiatric or sleep disorders;
  • Non-smoking for at least 6 months;
  • Body Mass Index of \>18 or \<30 kg/m2;
  • Able to maintain 7-hour consistent sleep schedule during the study
  • Able to refrain from caffeine, alcohol, medication and supplements during the study

You may not qualify if:

  • History of alcohol or substance abuse;
  • positive result on drugs of abuse urine toxicology;
  • Current or past history of sleep disorders, including but not limited to obstructive sleep apnea, narcolepsy, insomnia, or any significant sleep complaint
  • Psychiatric disorder, or first degree relative with a psychiatric disorder
  • Recent acute or chronic medical disorder
  • Use of drugs or medication (birth control OK) likely to affect sleep, alertness or light sensitivity, as determined by the investigators
  • Visual disorder, including but not limited to color blindness, or family history of glaucoma
  • Pregnancy or lactation
  • Shift work (\> 2 nights / week in the last 3 months and not during the study)
  • Transmeridian travel (2 or more time zones) in the past 3 months
  • Any other reason as determine by the Principal Investigator

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Brigham and Women's Hospital

Boston, Massachusetts, 02115, United States

Location

Related Publications (1)

  • Grant LK, Crosthwaite PC, Mayer MD, Wang W, Stickgold R, St Hilaire MA, Lockley SW, Rahman SA. Supplementation of ambient lighting with a task lamp improves daytime alertness and cognitive performance in sleep-restricted individuals. Sleep. 2023 Aug 14;46(8):zsad096. doi: 10.1093/sleep/zsad096.

Study Officials

  • Shadab A Rahman, PhD, MPH

    Brigham and Women's Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Model Details: Randomized crossover
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Neuroscientist

Study Record Dates

First Submitted

February 4, 2021

First Posted

February 9, 2021

Study Start

March 1, 2021

Primary Completion

March 1, 2022

Study Completion

March 1, 2022

Last Updated

February 18, 2022

Record last verified: 2022-02

Data Sharing

IPD Sharing
Will not share

Locations