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Study of Psychological and Motor Effects of Testosterone in Adolescents With XXY/Klinefelter Syndrome (TestoXXY/KS)

Primary Purpose

Klinefelter Syndrome, XXY Syndrome

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Testosterone gel 1%
Placebo gel
Sponsored by
University of Colorado, Denver
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Klinefelter Syndrome focused on measuring Klinefelter syndrome, XXY syndrome, Sex Chromosome Abnormality, Testosterone replacement therapy

Eligibility Criteria

8 Years - 18 Years (Child, Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Males with 47,XXY
  • Participants must be in early puberty (Tanner stage II-III)
  • Age 8 - 18 will be considered, but eligibility will be determined by review of laboratory results, bone age X-ray, and physical examination to determine stage of puberty
  • All racial and ethnic groups

Exclusion Criteria:

  • Other genetic variations of Klinefelter syndrome (48,XXXY, 48,XXYY, 49,XXXXY). The investigator has other studies for these groups and we encourage interested individuals with these disorders to contact us about other available studies.
  • 47,XXY plus another genetic disorder
  • Non-English speaking individuals (because the psychological tests are administered in English)
  • Participants with a medical history of blood clotting problems, blindness, deafness, or cancer

Sites / Locations

  • Childrens Hospital Colorado

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Testosterone gel 1%

Placebo gel

Arm Description

Testosterone gel 1% applied to skin once per day for 1 year. Starting dose 1.25mL per day, titrated in 1.25mL increments for 1st 6 months of study after each study visit up to maximum of 5.0mL per day. Titration based on testosterone levels with target level in mid-range of normal for Tanner stage.

Placebo gel applied to skin once per day for 1 year. Starting dose 1.25mL per day. Dose randomly adjusted in 1.25mL increments for 1st 6 months of study after each study visit up to maximum of 5.0mL per day.

Outcomes

Primary Outcome Measures

Change From Baseline on the Delis-Kaplan Executive Function System
A collection of subtests from the Delis-Kaplan Executive Function System will be used to evaluate different domains of executive functions including planning, problem solving, fluency, inhibition, and working memory. Possible scaled scores range from 0-20 (mean of 10), with higher scores indicating better performance. The value of the change in scaled score from baseline is reported.
Change From Baseline on the Bruininks-Oseretsky Test of Motor Development - 2
This test evaluates many aspects of motor functioning including fine and gross motor skills, visual motor integration, motor planning, and motor coordination. Possible scores range from 20-80, with higher scores indicating a better outcome.
Change From Baseline on the Conners Parent Rating Scales: DSM Attention
This questionnaire allows parents to rate many aspects of behavior including attention, hyperactivity, anxiety, social skills, and emotional lability. The range of possible scores is 0 to 100 (Mean T-score 50), with higher scores indicating a worse outcome.
Change From Baseline on the Conners Parent Rating Scales: DSM Hyperactivity
This questionnaire allows parents to rate many aspects of behavior including attention, hyperactivity, anxiety, social skills, and emotional lability. The range of possible scores is 0 to 100 (Mean T-score 50), with higher scores indicating a worse outcome.
Change From Baseline on the Conners Parent Rating Scales: Anxiety
This questionnaire allows parents to rate many aspects of behavior including attention, hyperactivity, anxiety, social skills, and emotional lability. The range of possible scores is 0 to 100 (Mean T-score 50), with higher scores indicating a worse outcome.
Change From Baseline on the Conners Parent Rating Scales: Social Skills
This questionnaire allows parents to rate many aspects of behavior including attention, hyperactivity, anxiety, social skills, and emotional lability. The range of possible scores is 0 to 100, with higher scores indicating a worse outcome.
Change From Baseline on the Conners Parent Rating Scales: Emotional Lability
This questionnaire allows parents to rate many aspects of behavior including attention, hyperactivity, anxiety, social skills, and emotional lability. The range of possible scores is 0 to 100, with higher scores indicating a worse outcome.

Secondary Outcome Measures

Change From Baseline on the Vineland Adaptive Behavior Scales - 2nd Edition
The Vineland-2 is an interview evaluating adaptive skills in the areas of communication, daily living skills, social skills, and motor skills. Possible scores range from 20 to 160 (mean 100), with higher scores indicating a better outcome.
Change From Baseline on the Wechsler Intelligence Scale for Children - Fourth Edition
This standardized assessment of cognitive functioning allows for evaluation of verbal and nonverbal cognitive skills, working memory, and processing speed. Possible full scale IQ scores range from 40-180 (mean 100), with higher scores indicating a better outcome.
Change From Baseline on the Comprehensive Test of Phonological Processing
This standardized test evaluates reading and language skills. Possible scores range from 20-200 (Mean Standard Score 100), with higher scores indicating a better outcome.

Full Information

First Posted
March 30, 2012
Last Updated
July 16, 2021
Sponsor
University of Colorado, Denver
Collaborators
Colorado Clinical & Translational Sciences Institute, Children's Hospital Colorado, National Institute of Neurological Disorders and Stroke (NINDS)
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1. Study Identification

Unique Protocol Identification Number
NCT01585831
Brief Title
Study of Psychological and Motor Effects of Testosterone in Adolescents With XXY/Klinefelter Syndrome
Acronym
TestoXXY/KS
Official Title
Psychological and Motor Effects of Testosterone Therapy in Adolescents With XXY/Klinefelter Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Completed
Study Start Date
March 2012 (undefined)
Primary Completion Date
October 2017 (Actual)
Study Completion Date
October 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Colorado, Denver
Collaborators
Colorado Clinical & Translational Sciences Institute, Children's Hospital Colorado, National Institute of Neurological Disorders and Stroke (NINDS)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine if testosterone replacement therapy leads to changes in psychological factors and/or motor skills in adolescent males with 47,XXY (also called Klinefelter syndrome). This study will also evaluate whether certain genetic factors of the X chromosome affect the psychological or motor features of XXY/Klinefelter syndrome.
Detailed Description
Klinefelter syndrome (47,XXY) is the most common chromosomal abnormality in humans and occurs in approximately 1 in 650 males. Testosterone deficiency develops during adolescence in the majority of individuals with XXY. However, there are no previous studies that evaluate the psychological and motor effects of testosterone replacement therapy in adolescents with XXY. The study researchers are interested in learning if testosterone therapy initiated in early puberty in XXY (KS) will lead to improvements in psychological and/or motor skills. They are also interested in learning if genetic variations of the androgen receptor gene or the parent-of-origin of the extra X chromosome influence the response to testosterone therapy. Specific psychological factors to be studied include verbal and nonverbal cognitive skills, attention, executive function (organization, problem-solving skills, inhibition), anxiety, language, self-esteem, and other behavioral factors. Motor skills to be studied include gross and fine motor skills, motor coordination, and motor planning. Participants in the study will be randomized to one of two treatment groups, receiving either testosterone gel or placebo, for 12 months. 60% of the study group will receive testosterone, and 40% will receive placebo. The research participants, parents/caregivers, and the members of the study team will be blinded to the treatment group, and will not know whether they are receiving testosterone gel or placebo treatments. The supervising endocrinologist for the study will not be blinded and will know which patients are in the testosterone and placebo groups. This will allow him to monitor results to determine if participants in the placebo group may develop a significant need for testosterone therapy during the study period. If this occurs, the patient will be switched to the testosterone group and will continue to be monitored in the study. All participants will be evaluated at the beginning of the study and at 1, 3, 6, and 12 months. Travel costs are included. Evaluations will include a combination of psychological and motor skills testing, questionnaires completed by the parent/caregiver and study participant, physical examinations, and blood draws for safety monitoring and genetic studies. Participation in the trial will last one year and includes 5 clinic visits to the eXtraordinarY Kids Clinic at Children's Hospital Colorado in Denver.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Klinefelter Syndrome, XXY Syndrome
Keywords
Klinefelter syndrome, XXY syndrome, Sex Chromosome Abnormality, Testosterone replacement therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
48 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Testosterone gel 1%
Arm Type
Experimental
Arm Description
Testosterone gel 1% applied to skin once per day for 1 year. Starting dose 1.25mL per day, titrated in 1.25mL increments for 1st 6 months of study after each study visit up to maximum of 5.0mL per day. Titration based on testosterone levels with target level in mid-range of normal for Tanner stage.
Arm Title
Placebo gel
Arm Type
Placebo Comparator
Arm Description
Placebo gel applied to skin once per day for 1 year. Starting dose 1.25mL per day. Dose randomly adjusted in 1.25mL increments for 1st 6 months of study after each study visit up to maximum of 5.0mL per day.
Intervention Type
Drug
Intervention Name(s)
Testosterone gel 1%
Other Intervention Name(s)
Androgel 1%
Intervention Description
Testosterone gel will be administered on a daily basis. The gel will be dispensed in a syringe, and the specific amount of gel to be applied each day will be determined by the study endocrinologist after reviewing labs.
Intervention Type
Drug
Intervention Name(s)
Placebo gel
Intervention Description
The placebo gel will be administered on a daily basis. The gel will be dispensed in a syringe, and the specific amount of gel to be applied each day will be determined by the study endocrinologist.
Primary Outcome Measure Information:
Title
Change From Baseline on the Delis-Kaplan Executive Function System
Description
A collection of subtests from the Delis-Kaplan Executive Function System will be used to evaluate different domains of executive functions including planning, problem solving, fluency, inhibition, and working memory. Possible scaled scores range from 0-20 (mean of 10), with higher scores indicating better performance. The value of the change in scaled score from baseline is reported.
Time Frame
Visit 1 (baseline) and Visit 5 (1 year)
Title
Change From Baseline on the Bruininks-Oseretsky Test of Motor Development - 2
Description
This test evaluates many aspects of motor functioning including fine and gross motor skills, visual motor integration, motor planning, and motor coordination. Possible scores range from 20-80, with higher scores indicating a better outcome.
Time Frame
Visit 1 (baseline) and Visit 5 (1 year)
Title
Change From Baseline on the Conners Parent Rating Scales: DSM Attention
Description
This questionnaire allows parents to rate many aspects of behavior including attention, hyperactivity, anxiety, social skills, and emotional lability. The range of possible scores is 0 to 100 (Mean T-score 50), with higher scores indicating a worse outcome.
Time Frame
Visit 1 (baseline) and Visit 5 (1 year)
Title
Change From Baseline on the Conners Parent Rating Scales: DSM Hyperactivity
Description
This questionnaire allows parents to rate many aspects of behavior including attention, hyperactivity, anxiety, social skills, and emotional lability. The range of possible scores is 0 to 100 (Mean T-score 50), with higher scores indicating a worse outcome.
Time Frame
Visit 1 (baseline) and Visit 5 (1 year)
Title
Change From Baseline on the Conners Parent Rating Scales: Anxiety
Description
This questionnaire allows parents to rate many aspects of behavior including attention, hyperactivity, anxiety, social skills, and emotional lability. The range of possible scores is 0 to 100 (Mean T-score 50), with higher scores indicating a worse outcome.
Time Frame
Visit 1 (baseline) and Visit 5 (1 year)
Title
Change From Baseline on the Conners Parent Rating Scales: Social Skills
Description
This questionnaire allows parents to rate many aspects of behavior including attention, hyperactivity, anxiety, social skills, and emotional lability. The range of possible scores is 0 to 100, with higher scores indicating a worse outcome.
Time Frame
Visit 1 (baseline) and Visit 5 (1 year)
Title
Change From Baseline on the Conners Parent Rating Scales: Emotional Lability
Description
This questionnaire allows parents to rate many aspects of behavior including attention, hyperactivity, anxiety, social skills, and emotional lability. The range of possible scores is 0 to 100, with higher scores indicating a worse outcome.
Time Frame
Visit 1 (baseline) and Visit 5 (1 year)
Secondary Outcome Measure Information:
Title
Change From Baseline on the Vineland Adaptive Behavior Scales - 2nd Edition
Description
The Vineland-2 is an interview evaluating adaptive skills in the areas of communication, daily living skills, social skills, and motor skills. Possible scores range from 20 to 160 (mean 100), with higher scores indicating a better outcome.
Time Frame
Visit 1 (baseline) and Visit 5 (1 year)
Title
Change From Baseline on the Wechsler Intelligence Scale for Children - Fourth Edition
Description
This standardized assessment of cognitive functioning allows for evaluation of verbal and nonverbal cognitive skills, working memory, and processing speed. Possible full scale IQ scores range from 40-180 (mean 100), with higher scores indicating a better outcome.
Time Frame
Visit 1 (baseline) and Visit 5 (1 year)
Title
Change From Baseline on the Comprehensive Test of Phonological Processing
Description
This standardized test evaluates reading and language skills. Possible scores range from 20-200 (Mean Standard Score 100), with higher scores indicating a better outcome.
Time Frame
Visit 1 (baseline) and Visit 5 (1 year)

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
8 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Males with 47,XXY Participants must be in early puberty (Tanner stage II-III) Age 8 - 18 will be considered, but eligibility will be determined by review of laboratory results, bone age X-ray, and physical examination to determine stage of puberty All racial and ethnic groups Exclusion Criteria: Other genetic variations of Klinefelter syndrome (48,XXXY, 48,XXYY, 49,XXXXY). The investigator has other studies for these groups and we encourage interested individuals with these disorders to contact us about other available studies. 47,XXY plus another genetic disorder Non-English speaking individuals (because the psychological tests are administered in English) Participants with a medical history of blood clotting problems, blindness, deafness, or cancer
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nicole Tartaglia, MD
Organizational Affiliation
University of Colorado School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Childrens Hospital Colorado
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80045
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
32542985
Citation
Davis SM, DeKlotz S, Nadeau KJ, Kelsey MM, Zeitler PS, Tartaglia NR. High prevalence of cardiometabolic risk features in adolescents with 47,XXY/Klinefelter syndrome. Am J Med Genet C Semin Med Genet. 2020 Jun;184(2):327-333. doi: 10.1002/ajmg.c.31784. Epub 2020 Jun 16.
Results Reference
derived
Links:
URL
http://www.genetic.org
Description
KS&A supports individuals with XXY/Klinefelter syndrome and other X&Y chromosome variations
URL
http://www.childrenscolorado.org/conditions/behavior/xychromosome.aspx
Description
The eXtraordinary Kids Clinic at Children's Hospital Colorado is a multispecialty clinic that evaluates and treats children, adolescents, and young adults with all X&Y chromosome variations

Learn more about this trial

Study of Psychological and Motor Effects of Testosterone in Adolescents With XXY/Klinefelter Syndrome

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