Multidimensional Measurement of Psychopharmacological Treatment Response

NCT ID: NCT01184235

Last Updated: 2014-01-06

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

44 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-08-31

Study Completion Date

2011-08-31

Brief Summary

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The study examines actigraphic, observational, psychometric and associated repeated measurements obtained prior to and during psychopharmacological treatment.

Detailed Description

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Baseline actigraphic measurements, multi-symptom operationally defined observations and psychometric data will be established and repeated to measure treatment response. Additional biological and biometric measures that have potential to further characterize the cohorts under study or treatment response will be collected as practical and when possible.

Conditions

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Autism Spectrum Disorders Mood Disorders Sleep Disorders Attention Deficit Disorders

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Autism Spectrum Disorders

This group will include those receiving or anticipating receiving pharmacological intervention whose primary diagnosis is Autism Spectrum Disorder

Pharmacological Intervention

Intervention Type DRUG

This study will include those anticipating or receiving any pharmacological intervention

Attention Deficit Hyperactivity Disorder

This group will include those receiving or anticipating receiving pharmacological intervention whose primary diagnosis is Attention Deficit Hyperactivity Disorder.

Pharmacological Intervention

Intervention Type DRUG

This study will include those anticipating or receiving any pharmacological intervention

Unaffected 1st Degree Relatives

This group will include unaffected, non treated first degree relatives of this study's subjects receiving or anticipating receiving pharmacological intervention.

No interventions assigned to this group

Mood Disorders

This group will include those receiving or anticipating receiving pharmacological intervention whose primary diagnosis is mood disorder.

Pharmacological Intervention

Intervention Type DRUG

This study will include those anticipating or receiving any pharmacological intervention

Interventions

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Pharmacological Intervention

This study will include those anticipating or receiving any pharmacological intervention

Intervention Type DRUG

Other Intervention Names

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antipsychotics antidepressants mood stabilizers stimulants NMDA antagonists

Eligibility Criteria

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Inclusion Criteria

* Diagnosis of:
* Autism Spectrum Disorder
* Mood Disorder
* Attention Deficit Hyperactivity Disorder
* Unaffected First Degree Relative of Study Subject
* Anticipation of pharmacological intervention or current pharmacological intervention

Exclusion Criteria

Inability to wear an actigraphy watch
Minimum Eligible Age

6 Months

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Child Psychopharmacology Institute

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Bill J Duke, M.A., Ph.D.

Role: PRINCIPAL_INVESTIGATOR

Child Psychopharmacology Institute

Robert D Staton, Ph.D., M.D.

Role: PRINCIPAL_INVESTIGATOR

Child Psychopharmacology Institute

Locations

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Child Psychopharmacology Institute

Fargo, North Dakota, United States

Site Status

Countries

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United States

References

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B. Duke and D. Staton,

Reference Type RESULT

Other Identifiers

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Act3

Identifier Type: -

Identifier Source: org_study_id

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