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NCT03805334 · ClinicalTrials.gov registry record · NA

The Effectiveness of Bilateral Alternating Tactile Stimulation for Improving Sleep in Children

A NA study, sponsored by Virginia Commonwealth University.

Completed
Registry status
NA
Development phase
3
Enrollment target

NCT03805334: Completed NA study, sponsored by Virginia Commonwealth University.

NCT03805334 is a NA study that has completed, run by Virginia Commonwealth University. The registered enrollment target is 3 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03805334, a NA study, has completed, sponsored by Virginia Commonwealth University.

COMPLETED
Registry status
NA
Development phase
3 participants
Enrollment target

Study Summary

The investigators hypothesize that wearing bilateral therapeutic vibrating devices before bed will result in positive changes in outcome measures related to sleep (e.g., sleep efficiency) in children who are sensitive to stimuli in their environment (aka sensory over responsiveness or SOR).

Primary Outcome

The Short Sensory Profile 2 is a caregiver questionnaire for children ages 3-14 years. It draws questions from the Child Sensory Profile 2 which measures sensory processing on two intersecting scales: high vs. low threshold for responding to sensations and passive vs. active self-regulation in anticipation or response to sensory stimuli. The Short Sensory Profile 2 is primarily used for research and screening purposes while the Child Sensory Profile 2 is for clinical practice. The investigators

Interventions

  • OTHER Touchpoints

Trial Details

FieldValue
Enrollment Target 3 participants
Start Date 2019-02-12
Est. Completion 2019-09-01
Phase NA
Virginia Commonwealth University

558 total trials

What the finished NCT03805334 record still lists

NCT03805334 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 3 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).

The record links to 0 conditions, and to 1 intervention - of which Touchpoints is the first listed.

NCT03805334 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03805334 about?

NCT03805334 is a clinical study titled "The Effectiveness of Bilateral Alternating Tactile Stimulation for Improving Sleep in Children". The investigators hypothesize that wearing bilateral therapeutic vibrating devices before bed will result in positive changes in outcome measures related to sleep (e.g., sleep efficiency) in children who are sensitive to stimuli in their environment (aka sensory over responsiveness or SOR).

What is the current status of trial NCT03805334?

This trial is currently completed. It is a NA study. The enrollment target is 3 participants. The study started on 2019-02-12. Estimated completion is 2019-09-01.

What interventions are being tested in trial NCT03805334?

The interventions under investigation include: Touchpoints (OTHER).

Who is sponsoring clinical trial NCT03805334?

This trial is sponsored by Virginia Commonwealth University, which has 558 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03805334's enrollment target sits among peer trials

3 1996th of 2000 higher than 4 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03805334, the US trial registry maintained by the National Library of Medicine. NCT03805334 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.