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Growth DisordersECROIPEDNCT07026812

Impact of Screens on Children's Growth

An observational study of Growth Disorders, run by University Hospital, Rouen at 1 site in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Short stature is defined as a height less than -2 Standard Deviations (SD) for age and a slowing of growth velocity by a loss of 1 SD/year. The causes of short stature are multiple (chronic diseases, growth hormone deficiency, hypothyroidism, hyperadrenocorticism, genetic syndromes, etc.). Read more about this study

Who is it for?
Ages 6 to 16 years
Conditions the study is for
Growth Disorders
How many people
150 participants
Where
1 siteFrance
Study dates
26 Sep 2022to 1 Jun 2025
How long will I take part?
1 Day
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 to 16 years
  • All sexes
  • No healthy volunteers
  • Child

Study population: Any patient coming to the day hospital for a growth hormone stimulation test and/or for an oral provocation test in the context of an allergy,

Who may be able to join

  • Children aged 6 to 16 years old coming to the day hospital for a growth hormone stimulation test or an oral provocation test (without growth disorders)
  • Not opposed to participating in the study
  • Patients affiliated with the Social Security system

Who cannot join

  • Growth hormone deficiency confirmed by 2 tests
  • Hypothyroidism
  • Hypercorticism
  • All chronic diseases
  • Skeletal pathologies: Turner syndrome, constitutional bone disease Intrauterine growth retardation
  • Pubertal delay defined by absence of puberty onset >13 years in girls and 14 years in boys
  • Patient under guardianship

Trial locations and contacts

1 site in 1 country.

France1 site
  • University Hospital of Rouen

    Rouen, 76031

Other trials in France

About this study

Short stature is defined as a height less than -2 Standard Deviations (SD) for age and a slowing of growth velocity by a loss of 1 SD/year. The causes of short stature are multiple (chronic diseases, growth hormone deficiency, hypothyroidism, hyperadrenocorticism, genetic syndromes, etc.). However, nearly 30% are considered idiopathic, with no identified etiology (Naccache et al., unpublished).

Growth hormone (GH) is secreted in a pulsatile manner with maximum peaks primarily at night, raising questions about the relationship between sleep disturbances and short stature.

In children, one of the main causes of sleep disturbances in the digital age is screen use, which is becoming increasingly important, particularly in the pediatric population.

Read the detailed description

During the night, physiologically, the retina, which no longer receives light signals, sends a message to the suprachiasmatic nucleus, the main key element of the internal clock, and to the pineal gland, which synthesizes melatonin, the sleep hormone. Exposing screens to blue light therefore disrupts melatonin secretion, which leads to a disruption of the circadian rhythm and therefore sleep. Note that this effect of light on melatonin secretion depends on the time of day of exposure, the intensity, and the duration. Thus, exposure to screens before bedtime can be responsible for a delay or even an absence of melatonin synthesis, particularly in the case of nighttime awakenings.

While many studies have examined the impact of screens on children's psychological balance, weight, etc., none, to our knowledge, has examined the potential impact of screens on children's height growth. Hypothesis of this project: 70% of GH synthesis takes place at night, a few minutes after entering slow-wave sleep, sleep disturbed by screens could mean a lower secretion of GH and consequently a delay in height growth.

The objective of this project is to evaluate the impact of screen consumption on sleep and the impact of sleep on idiopathic growth disorder.

Keywords
Growth hormone
Medical subject headings
Growth Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07026812
Study groupRoleWhat they receive
Growth hormone stimulation test groupNot described

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Screen consumption on sleep

    Evaluation of the Impact of Screen Consumption on Sleep by Answers to the Questionnaire Given to the Child and/or Parent(s) (Depending on Age)

    Measured: At enrollment visit

  2. Screen consumption on sleep

    Sleep assessment by responses to the questionnaire given to the child and/or the parent(s) (depending on age) in order to assess the duration of sleep

    Measured: At enrollment visit

  3. Screen consumption on sleep

    Evaluation of the Impact of Screen Consumption on Sleep by Answers to the Questionnaire Given to the Child and/or Parent(s) (Depending on Age) in Order to Evaluate child's physical activity

    Measured: At enrollment visit

  4. Impact of sleep on idiopathic growth disorder

    Collection of auxological data at the time of the day hospital consultation (height) noted in the health record and/or in the hospital medical file

    Measured: At enrollment visit

  5. Impact of sleep on idiopathic growth disorder

    Collection of auxological data at the time of the day hospital consultation (weight) noted in the health record and/or in the hospital medical file

    Measured: At enrollment visit

  6. Impact of sleep on idiopathic growth disorder

    Collection of auxological data at the time of the day hospital consultation (age) noted in the health record and/or in the hospital medical file

    Measured: At enrollment visit

Secondary outcomes (1)
  1. Impact of screens on body size (BMI)

    Evaluation of the impact of screens on body size (BMI) by response to the questionnaire given to the child and/or the parent(s)

    Measured: At enrollment visit

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Jun 2025
  2. Study start26 Sep 2022
  3. Primary completion11 Sep 2024
  4. Study completion1 Jun 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Prospective
Enrolment
150 participants (actual)
Target duration
1 Day
IDs, dates and publications
ClinicalTrials.gov ID
NCT07026812
Sponsor's protocol ID
2021/138/OB
Other IDs
ID RCB : 2021-A01115-36
Acronym
ECROIPED
Status last verified
Jan 2025
First submitted
10 Jun 2025
Last updated
18 Jun 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: The data provided will be the property of the sponsor and will be used solely for its own research activities.

Questions about this trial

What is this clinical trial studying?

An observational study of Growth Disorders, run by University Hospital, Rouen at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 18 Jun 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Screen consumption on sleep (time frame: At enrollment visit). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Jun 2025.

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