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CompletedNCT02053012Updated Apr 10, 2018

Investigating Reaction Time Among Children Who Snore

An observational study in Snoring, sponsored by Vidya Raman. Completed at 1 site in United States. Open to participants aged 6 Years to 18 Years. Per ClinicalTrials.gov, last updated 2018-04-10.

Sponsored by Vidya Raman · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
93
Ages
6 Years to 18 Years
Sex
All
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Study summary

The investigators feel that children who have OSA or sleep-disordered breathing may have a different reaction time than normal variants. Children who have OSA are known to have behavioral and sleep patterns that are different. It makes sense their reaction time may be different than normal as well. We plan to measure reaction times via a 10 minute psychomotor vigilance test device in children who snore who are coming in for a sleep study or for adenotonsillectomy.

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Conditions studied

  • Snoring

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03

In context

Snoring

122 studies on the registry are indexed under Snoring; 15 are open to participants now.

This study's enrollment of 93 is close to the median of 100 across 22 observational studies indexed under Snoring.

Browse Snoring studies →

Lead sponsor

Vidya Raman is the lead sponsor of 9 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
6 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Children who snore and are coming to Nationwide Children's for a sleep study or adenotonsillectomy.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Ability to understand how to perform reaction time test and complete without assistance.

Exclusion criteria

Exclusion Criteria:

  • Children who are unable to understand or perform test or parents refusal.
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
93 participants (actual)
Patient registry
No

Groups and cohorts

  • PVT-192

    Device: PVT-192

Interventions

  • DevicePVT-192

    PVT-192 Psychomotor Vigilance Task Monitor is a hand-held, self-contained system used for repetitive reaction time measurement.

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What researchers measure

Primary outcomes

  1. Reaction time

    We plan to measure reaction times via a 10 minute psychomotor vigilance test (PVT, Ambulatory Monitoring Inc., NY) device.

    Time frame: 10 minutes

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Study locations

1 site
  • Nationwide Children's Hospital
    Columbus, Ohio 43205, United States
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 10, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02053012
Lead sponsor
Vidya Raman
Responsible party
Vidya Raman (Clinical Assistant Professor, Nationwide Children's Hospital) — Sponsor-investigator
First posted
Feb 3, 2014
Start date
Jan 2014
Primary completion
Feb 23, 2018
Completion
Feb 23, 2018
Last update
Apr 10, 2018

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2018. You cannot join it, but the record below documents what was studied.

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Discussion

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