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Klinefelter SyndromeNCT03396562

The eXtroardinarY Babies Study: Natural History of Health and Neurodevelopment in Infants and Young Children With Sex Chromosome Trisomy

An observational study of Klinefelter Syndrome and Trisomy X, run by University of Colorado, Denver at 2 sites in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This study is designed to research the natural history of neurodevelopment, health and early hormonal function in infants with XXY/Klinefelter syndrome, XYY, XXX and other sex chromosome variations in an effort to identify early predictors of developmental and health outcomes. Read more about this study

Who is it for?
Ages 6 weeks to 13 months
Conditions the study is for
Klinefelter Syndrome, Trisomy X, XYY Syndrome
What is being tested?
Assessments of Development and Growth
How many people
300 participants
Where
2 sitesUnited States
Study dates
29 Sep 2017to 1 Mar 2028
Phase
Observational
Are there results?
Not yet: the study is under way

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 weeks to 13 months
  • All sexes
  • No healthy volunteers
  • Child

Study population: Sex Chromosome Trisomies (SCT) including Klinefelter (XXY), Trisomy X (XXX), and XYY. Rare sex tetrasomy and pentasomy conditions are also eligible.

Who may be able to join

  • Prenatal diagnosis of sex chromosome aneuploidy (by cfDNA, chorionic villi sampling, and/or amniocentesis)
  • Postnatal confirmatory karyotype of XXY, XYY, XXX, XXYY, XYYY, XXXY, XXXX, XXXXX, XXXXY, XXXYY, XXYYY, XYYYY (including any mosaicism with <80% 46,XX or 46,XY cell line)
  • English or Spanish speaking
  • Age 6 weeks to 12 months 30 days on enrollment

Who cannot join

  • Previous diagnosis of a different genetic or metabolic disorder with neurodevelopmental or endocrine involvement
  • Prematurity less than 34 weeks gestational age
  • Complex congenital malformation not previously associated with sex chromosome aneuploidy
  • History of significant neonatal complications (ie intraventricular hemorrhage, meningitis, hypoxic-ischemic encephalopathy)
  • Known complex Central Nervous System (CNS) malformation identified by neuroimaging

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Susan Howell, MS, CGC, MBA contact

720-777-8361

susan.howell@childrenscolorado.org

United States2 sites, 2 recruiting
  • Children's Hospital Colorado

    Aurora, Colorado, 80045

    Susan Howell, MS, CGC, MBA, 720-777-8361, susan.howell@childrenscolorado.org

    Mariah Brown, (720)777-6774, mariah.brown2@childrenscolorado.org

    Recruiting
  • Nemours at Thomas Jefferson University

    Philadelphia, Pennsylvania, 19107

    Judith Ross, MD, 215-955-1648, jlross@nemours.org

    Karen Kowal, PAC, 215-9559008, karen.kowal@nemours.org

    Recruiting

Other trials in United States

About this study

This study is designed to research the natural history of neurodevelopment, health and early hormonal function in infants with XXY/Klinefelter syndrome, XYY, XXX and other sex chromosome variations in an effort to identify early predictors of developmental and health outcomes. The Investigators will also evaluate different developmental screening tools in infants with sex chromosome variations so the investigators can develop recommendations for pediatrician caring for infants and young children with XXY/Klinefelter syndrome, XYY, XXX, and other sex chromosome variations.

Read the detailed description

Background: Sex Chromosome Trisomies (SCT) including Klinefelter (XXY), Trisomy X (XXX), and XYY syndromes occur in 1 out of every 500 births and are associated with a broad phenotypic spectrum including increased risk for developmental delays (DD), language/learning disorders, and autism spectrum disorder (ASD). XXY is also associated with testicular failure, XXX increases risk for ovarian failure, and disorders of insulin resistance and other medical problems resulting in increased morbidity and mortality occur in all 3 SCTs. Historically, less than 10% of SCT diagnoses occur in childhood, however the rate of newborns with SCT has markedly increased with new noninvasive prenatal cell-free DNA (cfDNA) screening. SCT natural history research is limited to studies from the 1970's, and the investigators have little knowledge of early predictors of the wide heterogeneity in later outcomes. The high risk for DD in SCT suggests that newborn screening may improve identification for DD and timely initiation of interventions. However, it is not clear whether all SCT infants indeed require intensive developmental assessments and therapies, or if primary care screenings are sufficient to identify those in need. The surge in prenatal SCT diagnoses from cfDNA methods provides an opportunity for longitudinal study of a cohort of infants to explore natural history, and to improve care.

Aims: This study aims to: (1) describe and compare the natural history of neurodevelopment, health and early gonadal function in infants with the 3 SCT conditions through a national prospective eXtraordinarY Babies Study in partnership with the Newborn Screening Translational Research Network (NBSTRN), (2) identify early predictors of poor neurodevelopmental and cardiometabolic outcomes, and (3) evaluate the sensitivities of common primary care developmental screening measures to detect DD and ASD in this high-risk population to inform recommendations for an early neurodevelopmental care protocol.

Approach: Infants with a prenatal diagnosis of XXY, XYY, or XXX will be followed prospectively every 6-12 months for 2-4 years at 2 eXtraordinarY Kids Clinic sites. Demographics, health history, development, interventions, and social/family history will be collected. Assessments will include: (1) measures of cognitive, language, social, motor, and adaptive function, (2) physical exam, gonadal function labs, cardiometabolic measures, and body composition, and (3) quality of life outcomes. Impact: Prospective study of the natural history of prenatally diagnosed infants with SCT will allow investigation of important questions to inform newborn screening considerations, such as the interplay between early hormonal profiles and developmental outcomes. Results will be immediately relevant for counseling and establishing evidence-based care guidelines for the rapidly increasing rate of SCT diagnoses from cfDNA screening. Results will serve as the basis for ongoing longitudinal studies of health and psychological outcomes of SCTs through the lifespan.

Being tested
Assessments of Development and Growth
Keywords
body composition, klinefelter syndrome, XXY, Trisomy X, XXX, XYY, XXYY, XXXY, XXXXY, sex chromosome variation, sex chromosome aneuploidy, sex chromosome trisomy, testosterone, XYYY, XXXX, XXXXX, XXXYY, XXYYY, XYYYY, developmental delay
Medical subject headings
Klinefelter Syndrome, Triple X syndrome, 47, XYY syndrome, Tetrasomy X, 49,XXXXX syndrome, Learning Disabilities

What participants receive

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

  • Assessments of Development and GrowthOther

    Longitudinal observational assessments of development and growth at ages: 2 months, 6 months, 12 months, 18 months, 24 months, 36 months, 48 months, 5 years, 6 years, 7 years, 8 years, 9 years of age.

Study groups in NCT03396562
Study groupRoleWhat they receive
SCT ConditionsSex Chromosome Trisomies Conditions including Klinefelter (XXY), Trisomy X (XXX), XXY Syndromes. Interventions: Longitudinal observational assessments of development and growth at ages: 2 months, 6 months, 12 months, 18 months, 24 months, 36 months, 48 months, and 5 or 6 years.
Receives: Other: Assessments of Development and Growth

What is being measured

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

  1. Longitudinal Descriptive Statistics of Cognitive Scores on the Bayley-III

    Cognitive skills will be assessed using the standardized Bayley Scales of Infant Development--3rd Edition (Bayley-3)

    Measured: 36 months

  2. Longitudinal Descriptive Statistics of Motor Scores on the Bayley-III

    Motor development will be assessed using the standardized Bayley Scales of Infant Development--3rd Edition (Bayley-3)

    Measured: 36 months

  3. Longitudinal Descriptive Statistics of Language Scores on Bayley-III

    Language development will be assessed using the Bayley Scales of Infant Development--3rd Edition (Bayley-3)

    Measured: 36 months

Secondary outcomes (3)
  1. Body Mass Index (BMI)

    BMI will be determined through measurement of length and weight at the research visit.

    Measured: 36 months

  2. Z Score

    The z score will be calculated for age group at the research visit.

    Measured: 36 months

  3. Body Composition (% body fat)

    Body fat percentage will be measured using air Dual Energy X-Ray Absorptiometry (DEXA) at 3 year old visit.

    Measured: 3 year old visit

Timeline

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

  1. First posted11 Jan 2018
  2. Study start29 Sep 2017
  3. Primary completion1 Mar 2028 (estimated)
  4. Study completion1 Mar 2028 (estimated)

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
300 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03396562
Sponsor's protocol ID
17-0118
Status last verified
May 2024
First submitted
5 Dec 2017
Last updated
9 May 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Klinefelter Syndrome and Trisomy X, run by University of Colorado, Denver at 2 sites in United States.

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 4 inclusion and 5 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: looking for participants now, as of the sponsor's last update on 9 May 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United States. 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?

This study is still under way. Results are not available in the source record yet.

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

Contact Nicole Tartaglia, MD, MS ((720) 777-8087, nicole.tartaglia@childrenscolorado.org), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Longitudinal Descriptive Statistics of Cognitive Scores on the Bayley-III (time frame: 36 months). The study lists 3 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 9 May 2024.

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