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OpenTrials
Completed

NCT Number: NCT03508843

Improving Child Restraint Installation

The investigators will conduct a pre-post trial with 150 parents in rural South Central Montana. The study will recruit families to cooperating community locations (e.g., churches, public libraries) to participate in research evaluating the efficacy of parents installing restraints with guidance from a remotely-located technician using interactive virtual presence. Following informed consent procedures, parents will complete a brief survey on behaviors, attitudes, and perceptions about child safety and restraints while an on-site technician evaluates baseline safety of the restraint. Parents will then engage remotely using their personal smartphone with an off-site certified car seat technician, obtaining advice to install the child restraint properly via the HelpLightning interactive virtual presence app. Following the remote interaction, the on-site technician will again inspect the restraint using the validated checklist (and correct any errors prior to the participant leaving). The overall goal is to demonstrate installation of child restraints can be effectively accomplished to rural populations using interactive virtual presence. The study has 2 specific aims:

Specific Aim 1. Demonstrate technological and behavioral efficacy of providing instructions on child restraint installation remotely to rural populations. Demonstrate >95% of interactions proceed without technical problems, without reports of communication difficulty on either end of the exchange (the parent or the technician), and without interruption.

Specific Aim 2. Identify accuracy of child restraint installation by parents using instructions provided by a remotely-located certified technician via interactive virtual presence. Demonstrate installation in this manner achieves ≥90% accuracy across all aspects of child restraint installation. Demonstrate installation in this manner significantly reduces restraint installation errors.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

UAB Youth Safety Lab, University of Alabama at Birmingham

Birmingham, Alabama, 35294, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • communicate in English
  • drive a vehicle with one or more car seats present
  • willing to install a car seat into the vehicle

Exclusion criteria

  • none

Treatment and study plan

interactive virtual presence

Behavioral

installing the car seat with advice via interactive virtual presence

Primary outcomes

  1. Number of Participants Who Accurately Select a Safe Child Restraint

    Time frame: immediately (< 5 minutes) after the car seat is installed

    accurate selection of a safe child restraint that was proper for the child's age and size

  2. Number of Participants Who Install the Child Restraint Accurately Into the Vehicle

    Time frame: immediately (< 5 minutes) after the car seat is installed

    accurate installation of the child restraint into the vehicle

  3. Number of Participants Who Properly Position the Child Restraint in the Vehicle

    Time frame: immediately (< 5 minutes) after the car seat is installed

    proper positioning of the child restraint in the vehicle

Sponsors and collaborators

Lead sponsor

University of Alabama at Birmingham

Other

Registry information

Official study title

Improving Child Restraint Installation in Rural America Through Interactive Virtual Presence

Important dates

Study start
2018
Primary completion
2018
Study completion
2018
First posted
Apr 26, 2018
Registry last updated
Oct 18, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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