A Non-Drug Study of The Suitability of Neurocognitive Tests And Functioning Scales For The Measurement of Cognitive And Functioning Changes in Individuals With Down Syndrome

NCT ID: NCT01580384

Last Updated: 2015-03-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

90 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-02-29

Study Completion Date

2014-01-31

Brief Summary

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This non-drug, longitudinal, multi-center, multi-national study will evaluate the suitability of neurocognitive tests and functioning scales for the measurement of cognitive and functioning changes in individuals with Down Syndrome. Tests will be administered at clinic visits in Weeks 1, (4) and 24. The duration of the study for each individual will be between 24 and 27 weeks.

Detailed Description

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Conditions

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Down Syndrome

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Cohort

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Males and females, 12 to 30 years of age, with diagnosis of Down Syndrome
* Down Syndrome subjects meeting clinical diagnostic criteria for generalized anxiety disorders, major depressive disorders, autism spectrum disorder, attention deficit and hyperactivity disorder can participate in the study provided they are on stable medication for at least 8 weeks prior to screening and likely to cooperate and take part successfully in the study assessments

* Subjects who may not be able to comply with the protocol or perform the outcome measures due to significant hearing or visual impairment
* Subjects with evidence of dementia or meeting clinical diagnosis for dementia
* Subjects with thyroid dysfunction or diabetes that is not adequately controlled and stabilized on treatment for at least 8 weeks prior to randomization
Minimum Eligible Age

12 Years

Maximum Eligible Age

30 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hoffmann-La Roche

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Clinical Trials

Role: STUDY_DIRECTOR

Hoffmann-La Roche

Locations

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Tucson, Arizona, United States

Site Status

Durham, North Carolina, United States

Site Status

Ciudad Autonoma de Bs As, , Argentina

Site Status

Ciudad de Buenos Aires, , Argentina

Site Status

Kentville, Nova Scotia, Canada

Site Status

Paris, , France

Site Status

Saint-Etienne, , France

Site Status

Rome, Lazio, Italy

Site Status

Palermo, Sicily, Italy

Site Status

Barcelona, Barcelona, Spain

Site Status

London, , United Kingdom

Site Status

Redruth, , United Kingdom

Site Status

Countries

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United States Argentina Canada France Italy Spain United Kingdom

References

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Spiridigliozzi GA, Goeldner C, Edgin J, Hart SJ, Noeldeke J, Squassante L, Visootsak J, Heller JH, Khwaja O, Kishnani PS, Liogier d'Ardhuy X. Adaptive behavior in adolescents and adults with Down syndrome: Results from a 6-month longitudinal study. Am J Med Genet A. 2019 Jan;179(1):85-93. doi: 10.1002/ajmg.a.60685. Epub 2018 Dec 20.

Reference Type DERIVED
PMID: 30569586 (View on PubMed)

Other Identifiers

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BP25612

Identifier Type: -

Identifier Source: org_study_id

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