Digital Photography to Estimate Anthropometric Measurements in Children

September 14, 2023 updated by: Siobhan T. Pittock, Mayo Clinic

Use of Digital Photography to Estimate Anthropometric Measurements in Children

The purpose of this study is to see if photos taken from home can accurately let physicians know the height, abdominal circumference, and wrist circumference of children, and how these measurements relate to in-person measurements.

Study Overview

Status

Terminated

Conditions

Detailed Description

This study will occur in two distinct parts. Children age 2-18 who present to Mayo for an outpatient clinic appointment will be considered for participation in the study. Patients eligible for the study will receive a portal message the day prior to their appointment informing them of the option to take place in the study as well as instructions on how to measure height, abdominal circumference, and wrist circumference, and how to obtain and submit digital photographs. Participants can submit photographs and home measurements either before or after the in clinic measurements and photographs have been obtained. Those willing to participate will sign a parental consent form and a child assent form. Consent and assent forms can be seen in the supplemental documents.

At Home Participants will be given written instructions asking for 2 photographs to be submitted via the patient portal and for measurements of height, abdominal circumference, and wrist circumference to be obtained using a home tape measure. Detailed patient instructions will be shared.

Study Visit

Traditional Anthropometric Measurements Participant will have a height measurement using a calibrated stadiometer, a weight measurement taken on a scale, a waist circumference taken at the umbilicus, and a wrist circumference will be taken while seated on the dominant wrist over the Lister tubercle of the radius and over the distal ulna. Participants 5 years of age and older who are 90cm and greater will have body composition assessed by impedance. Bioelectrical impedance is not in any way uncomfortable and does not expose the participant to any radiation. Participant measurements will be recorded in the patient record and a secure excel document or in RedCap. Recruited patient's medical record number (MRN) will be documented in a secure excel document or in RedCap.

Digital Photography Measurements The participant will be instructed to take off any thick outer layers and leave on shirt and pants. Tops will be gathered to make cloth tight to body. The participant will stand next to an 8 ½" x 11" piece of paper taped to a wall, to use as a reference for linear regression calculations. The participant will have a photograph taken in the "Frankfurt plane" with lower border of the eyes in line with the external ear canal, palms facing forward and arms to the side, while taking a deep breath at the time of the photograph to have optimal stretching. A photograph will be taken from the side in the sagittal plane with palms facing down and arms outstretched in front of the patient while taking a deep breath at the time of the photograph for optimal stretching. These photos will be taken by a trained member of the research team.

Study Type

Interventional

Enrollment (Actual)

26

Phase

  • Not Applicable

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

    • Minnesota
      • Rochester, Minnesota, United States, 55905
        • Mayo Clinic in Rochester

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

2 years to 18 years (Child, Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Children age 2-18 years old.
  • Seen on Mayo 16 for an outpatient clinic appointment.

Exclusion Criteria:

  • Participant unable to stand for stadiometer height
  • Pregnant patients

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

  • Primary Purpose: Health Services Research
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Photography to Measure Children's Height, Wrist Circumference, and Abdominal Circumference
Subjects will be given instructions on how to take two photographs at home and submit them securely. Subjects will also be given instructions on how to measure height, wrist circumference, and waist circumference and submit this data to the research team.
The participant will be instructed to take off any thick outer layers and leave on shirt and pants. Tops will be gathered to make cloth tight to body. The participant will stand next to an 8 ½" x 11" piece of paper taped to a wall, to use as a reference for linear regression calculations.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Height
Time Frame: 1 day
Measured in cm
1 day
Abdominal circumference
Time Frame: 1 day
Measured in cm
1 day
Wrist circumference
Time Frame: 1 day
Measured in cm
1 day

Collaborators and Investigators

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

Sponsor

Investigators

  • Principal Investigator: Siobhan Pittock, M.B., B.Ch,, Mayo Clinic

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)

August 30, 2021

Primary Completion (Actual)

September 28, 2021

Study Completion (Actual)

September 28, 2021

Study Registration Dates

First Submitted

August 31, 2021

First Submitted That Met QC Criteria

August 31, 2021

First Posted (Actual)

September 5, 2021

Study Record Updates

Last Update Posted (Actual)

September 15, 2023

Last Update Submitted That Met QC Criteria

September 14, 2023

Last Verified

September 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 20-011901

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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