Testing the Feasibility of a Novel Growth Monitoring Smartphone App
1 other identifier
observational
146
1 country
1
Brief Summary
The goal of this clinical trial is to test the acceptability, feasibility, accuracy and precision of the 'GrowthMonitor' smartphone app in a pilot population.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Mar 2021
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 18, 2021
CompletedFirst Submitted
Initial submission to the registry
March 6, 2023
CompletedFirst Posted
Study publicly available on registry
April 25, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
January 31, 2025
CompletedMarch 10, 2025
March 1, 2025
3.9 years
March 6, 2023
March 7, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Reliability
Inter- and intra-rater reproducibility of the GrowthMonitor app
At baseline
Agreement
Agreement between the GrowthMonitor app and wall-fixed stadiometer
At baseline
Secondary Outcomes (1)
Usability
At 1 week
Eligibility Criteria
Patients attending prearranged new and follow-up outpatient appointments at the Children's Hospital at Barts Health Trust, London. Participants will be recruited through convenience sampling in order to maximize recruitment efforts during the time of the study. Data on gender, age, and height will be collected.
You may qualify if:
- Children and young people (male and female) aged 1-18 yr receiving height measurements as part of their routine / prearranged attendance to a paediatric endocrinology or other paediatric out-patient appointment at Barts Health Trust.
- Participants require a smartphone to take part in the study.
You may not qualify if:
- Children under the age of 1 years
- Young people aged 16-18yr who lack capacity to consent
- Other individuals unable to reliably stand for an accurate height measurement e.g.
- individuals with severe disability and/or confined to a wheelchair
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Barts Health NHS Trust
London, United Kingdom
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Helen Storr, PhD
Queen Mary University, London
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 6, 2023
First Posted
April 25, 2023
Study Start
March 18, 2021
Primary Completion
January 31, 2025
Study Completion
January 31, 2025
Last Updated
March 10, 2025
Record last verified: 2025-03
Data Sharing
- IPD Sharing
- Will not share