INSIGHTS: Inspiring New Science In Guiding Healthcare in Turner Syndrome Registry

Sponsor
University of Colorado, Denver (Other)
Overall Status
Recruiting
CT.gov ID
NCT05052606
Collaborator
(none)
5,000
6
64.4
833.3
12.9

Study Details

Study Description

Brief Summary

INSIGHTS is a registry research study that collects key information on medical history for girls and women with Turner syndrome and the clinical care they receive. This includes genetic tests, imaging, medications, and more for hundreds of patients seen at a number of clinics across the US. In addition to learning a lot about the current state of health for individuals with TS, INSIGHTS serves as an infrastructure to conduct future studies are meaningful to patients and their families.

Condition or Disease Intervention/Treatment Phase
  • Other: No intervention

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
5000 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
INSIGHTS Registry - Inspiring New Science In Guiding Healthcare in Turner Syndrome
Actual Study Start Date :
May 20, 2020
Anticipated Primary Completion Date :
Oct 1, 2025
Anticipated Study Completion Date :
Oct 1, 2025

Outcome Measures

Primary Outcome Measures

  1. Health conditions [From study start until condition observed, up to 15 years]

    Average number of chronic diagnoses per person

Secondary Outcome Measures

  1. Prevalence of mental health diagnoses [From study start until condition observed, up to 15 years]

    Prevalence of mental health diagnoses is defined as the number of participants in the sample diagnosed with a mental health disorder by a clinician according to their medical record out of the total sample. This will be determined by a diagnosis of any of the following in a clinical encounter, problem list, and/or past medical history: Depression Anxiety Mood disorder NOS Psychotic disorder Attention-deficit/hyperactivity disorder (ADHD) Autistic disorder

  2. Prevalence of premature ovarian insufficiency [From study start until condition observed, up to 15 years]

    Prevalence of premature ovarian insufficiency is defined as the number of participants in the sample with a diagnosis of premature ovarian insufficiency (or failure) in their medical record clinical encounter, problem list, and/or past medical history or laboratory results in their medical record consistent with this diagnosis (elevated FSH or undetectable AMH) out of the total sample.

  3. Prevalence of hearing loss [From study start until condition observed, up to 15 years]

    Prevalence of hearing loss is defined as the number of participants in the sample formally diagnosed with a hearing loss in their medical record in a clinical encounter, problem list, and/or past medical history or an audiology report consistent with hearing impairment out of the total sample.

  4. Cardiometabolic diagnoses - prevalence of obesity [From study start until condition observed, up to 15 years]

    Prevalence of obesity is defined as the number of participants in the sample with obesity in their medical record out of the total sample. Obesity in pediatric populations is determined using BMI-for-age and obesity in adult populations is determined using BMI. BMI is calculated as the weight in kilograms divided by the height in meters squared. Participants will be considered to have obesity if: There is a diagnosis of obesity in the medical record in a clinical encounter, problem list, and/or past medical history For children 17 years and younger: there is an available growth chart/height/weight/other data necessary to calculate the BMI-for-age and the BMI-for-age is at or above the 95th percentile For adults 18 years and older: there is a BMI at or above 30 kg/m2 or the data necessary to calculate BMI and it is at or above 30 kg/m2

  5. Cardiometabolic diagnoses - prevalence of dyslipidemia [From study start until condition observed, up to 15 years]

    Prevalence of metabolic syndrome is defined as the number of participants in the sample with dyslipidemia in their medical record out of the total sample. Dyslipidemia will be defined as: Diagnosis of dyslipidemia, hypertriglyceridemia, hypercholesterolemia in a clinical encounter, problem list, and/or past medical history Laboratory evidence of elevated total cholesterol, LDL, triglycerides, and/or low HDL for sex and age

  6. Cardiometabolic diagnoses - prevalence of fatty liver disease [From study start until condition observed, up to 15 years]

    Prevalence of fatty liver disease is defined as the number of participants in the sample with a formal diagnosis of fatty liver disease in their medical record out of the total sample. Fatty liver disease diagnosis in the medical record in a clinical encounter, problem list, and/or past medical history may also present as: Non-alcoholic fatty liver disease (NAFLD) Hepatic steatosis Simple fatty liver disease Non-alcoholic steatohepatitis

  7. Cardiometabolic diagnoses - prevalence of hypertension [From study start until condition observed, up to 15 years]

    Prevalence of hypertension is defined as the number of participants in the sample with evidence of hypertension in their medical record out of the total sample. Evidence of hypertension includes: Formal diagnosis of hypertension in a clinical encounter, problem list, and/or past medical history For children under 13 years old: a blood pressure reading at or above the 95th percentile for age, height, and sex For children between 13 and 17 years old: a blood pressure reading at or above 130/80 mmHg For adults 18 years or older: a blood pressure reading at or above 140/90 mmHg

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Individuals with TS and TS variants as defined by the TS Clinical Practice Guideline definition (karyotype consistent with TS, phenotypic female, clinical feature(s) of TS)

  2. Clinic visit at a participating center within the past 12 months (any specialty acceptable)

  3. Informed consent/assent as appropriate

Exclusion Criteria:
  1. Lack of a TS diagnosis on file

Contacts and Locations

Locations

Site City State Country Postal Code
1 Children's Hospital Colorado Aurora Colorado United States 80045
2 Children's National Washington District of Columbia United States 20010
3 Lurie Children's Glenview Illinois United States 60026
4 UNC Hospitals Children's Specialty Clinic Chapel Hill North Carolina United States 27514
5 Children's Hospital of Philadelphia Philadelphia Pennsylvania United States 19104
6 The University of Texas Health Science Center at Houston Houston Texas United States 77030

Sponsors and Collaborators

  • University of Colorado, Denver

Investigators

  • Principal Investigator: Shanlee M Davis, MD, PhD, Children's Hospital Colorado

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Colorado, Denver
ClinicalTrials.gov Identifier:
NCT05052606
Other Study ID Numbers:
  • 19-3027
First Posted:
Sep 22, 2021
Last Update Posted:
Sep 22, 2021
Last Verified:
Sep 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 22, 2021