Clinical Application and Functionality for an Application for Measurement of Head Circumference.

February 27, 2023 updated by: Mr Stefan Yordanov, University of Cambridge

Clinical Application and Functionality for an Application for Measurement of Head Circumference in Neonates and Children

Title of clinical study:Clinical application, validation, and functionality evaluation of the Mobile Head Circumference Application in neonates and children

Sponsor: University Hospitals NHS Foundation Trust

Purpose of study:Evaluate and validate the utility of the mobile Head Circumference application for use in the clinical and outpatient setting for evaluation of head circumference of neonates and infants

Primary objectives:Evaluate usefulness of and feasibility of the application in the clinical setting comparing it to normal practice.

Secondary objectives:Evaluate parent/guardian reliability and satisfaction of the use of the mobile head circumference app.

Study Design:Prospective

Sample Size:Treating clinicians employed by Cambridge University Hospitals NHS Foundation Trust will identify patients eligible for this study (infants <18 months of age) and notify research team members with the patient's/guardian's consent. Once identified, research team members will approach patients' parents/guardians to seek informed consent before their clinic appointment or at the bedside on the ward. An information sheet will be used. If they choose to participate, we will measure the HC during the clinic appointment or on the ward. (Please refer to Flowchart 1). Sample size estimation was calculated with 90% statistical power to detect a change of means by 1 and a standard deviation of 1. This, along with 10% iteration, equals 33 participants.

Summary of eligibility criteria:Neonatal patients and infants with need of continuous measurement of Head Circumference up to the age of 18months.

Investigational techniques:Mobile application for Automatic measurement of head circumference.

Study Overview

Status

Completed

Detailed Description

An accurate head circumference (HC) measurement is a quick and cost-effective assessment which is essential when clinically evaluating a neonate or infant. HC outside the normal range may indicate a disorder of brain development, hydrocephalus, or an intracranial mass lesion. The growth pattern of HC, determined from serial measurements, also provides useful clinical information. For example, changes in HC are used to help determine whether hydrocephalus needs treatment. HC growth is also predictive of neurodevelopmental outcomes. [Lippé et al. 2018]

HC is measured by measuring the widest circumference of the head with a tape measure. Typically, this is performed by health care workers, but parents can be taught to take measurements reliably. With the increasing use of telephone and virtual clinics as a substitute to face-to-face appointments, parental measurement of HC is increasingly used to help guide clinical management in a wide variety of clinical specialties including Neurosurgery, Neonatology, Paediatrics, and General Practice.

Tape measure HC measurements are prone to error, particularly when performed by parents, due to individual differences in head shape, hair style and texture, subject cooperation, and examiner differences in tape measure placement and tautness.6 There is therefore the need for a more reliable method.

Rationale for the study:

We have developed a HC mobile application (HCMA) that can measure the head circumference of an infant and plot it against standardised growth charts.

The rationale of this study is to validate the HCMA in a clinical setting and to review its usability by parents in the community.

Research objective and purpose

The main objective of the study is to validate the accuracy of the HC app and to prove its utility and feasibility in clinical practice.

Secondary objectives will be to evaluate parent/guardian reliability and satisfaction of using the HC app.

Primary Objective:

Hypothesis 1: There is no statistically significant difference between HC measured with a tape measure and HC measured with HCMA;

Secondary Objectives:

Hypothesis 2: Intra-rater Reliability(precision/repeatability) - The variability of series of three measurements of HC using HCMA (performed by a healthcare professional) is within 0.5 cm -(the standard error margin for measurement measurements) Hypothesis 3: Inter-rater Reproducibility - HC measurements made using the HCMA will not be significantly different when measured by parents or healthcare professionals we will then compare measurements of HC using HCMA performed by healthcare professional with the measurements performed by the parents/guardians using the HCMA. These should be within the standard error of margin for the measurement with tape measure.

Hypothesis 4: Parents are satisfied using the HCMA and find it easy to use'

Study Type

Observational

Enrollment (Actual)

37

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Cambridge, United Kingdom, CB2 0QQ
        • Addenbrookes Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

No older than 1 year (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Infants up to 18 months with neurological disorders(attending Neurosurgery Clinics)

Description

Inclusion Criteria:

  • Infants up to 18 months old seen in a paediatric clinic with a requirement for continuous head circumference measurements.

Exclusion Criteria:

  • Infants above the age of 18 months, Patients in emergency setting, Withdrawal of consent of parents/guardians

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Researcher
Patients will have their Head circumference measured with a tape and with the mobile phone app.
Measurement of Head circumference of Babies/Infants with a mobile phone application.
Parent
Patients will have their Head circumference measured with a tape and with the mobile phone app.
Measurement of Head circumference of Babies/Infants with a mobile phone application.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Criterion Validity(Vs Gold Standard)
Time Frame: Day 0
Proof of concept of that the HCMA is an accurate and precise tool for measuring HC compared to standard practice (tape measure);
Day 0

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Repeatability and reliability
Time Frame: Day 0
Within-rater variability using three consecutive measurements with HCMA by a health care professional;
Day 0
Reliability of parents/guardians in measurement of head circumference with a tape measure (supervised by a health care professional);
Time Frame: Day 0
Day 0
Reliability of parents/guardians in measurement of head circumference using the HCMA
Time Frame: Day 0
Day 0

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Ibrahim Jalloh, FRCS(Nsgy), University of Cambridge
  • Principal Investigator: Stefan Yordanov, MRCSed, University of Cambridge

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 1, 2022

Primary Completion (Actual)

January 15, 2023

Study Completion (Actual)

February 1, 2023

Study Registration Dates

First Submitted

May 16, 2022

First Submitted That Met QC Criteria

February 27, 2023

First Posted (Estimate)

March 10, 2023

Study Record Updates

Last Update Posted (Estimate)

March 10, 2023

Last Update Submitted That Met QC Criteria

February 27, 2023

Last Verified

February 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • Ver2

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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