Development of an Instrument That Monitors Behaviors Associated With OCD

August 10, 2016 updated by: University of Minnesota
To support the discovery of new means for revealing the presence of Obsessive Compulsive Disorder (OCD), facilitating detection through new technology-based metrics, and attempt to automate existing diagnostic procedures allowing for more efficient diagnostic methods that would broaden clinical scope and outreach.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Aim 1: To observe and compare childhood behaviors regarding handwashing in OCD and control populations

Hypothesis 1: Control participants will spend less time washing their hands, will wash them less frequently, and will be less preoccupied with the sink when doing other activities.

Aim 2: To observe and compare childhood behaviors regarding organizing a cluttered area.

Hypothesis 2: OCD participants will be more disturbed by the presence of clutter and more compelled to organize the items than control participants

Aim 3: To observe and compare childhood behaviors regarding turning on/off light switches

Hypothesis 3: OCD children will be more likely to exhibit compulsive repetitive behaviors regarding the light switch than control participants

Study Type

Observational

Enrollment (Actual)

40

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Minnesota
      • Minneapolis, Minnesota, United States, 55454
        • University of Minnesota

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

5 years to 17 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

The investigators will recruit 20 children and adolescents with OCD aged 5-17 who present to the University of Minnesota Child and Adolescent Anxiety and Mood Disorders Clinic or who are referred from outside clinicians. Twenty healthy controls will be recruited from the community.

Description

Inclusion Criteria:

  • Male and female children
  • Aged 5 to 17

Exclusion Criteria:

  • Inability or unwillingness to provide written informed consent/assent

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Healthy Controls
Observational Study: No intervention
OCD
Observational Study: No intervention

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Length of Handwashing
Time Frame: Same Day
Researchers blindly rate the how long (secs) it takes participants to wash their hands.
Same Day
Behaviors Associated with Handwashing
Time Frame: Same Day
Researchers blindly rate whether participants exhibit any unique behavior while washing their hands.
Same Day
Length of Free Arrangement
Time Frame: Same Day
Researchers blindly rate how long it takes participants to freely organize a box of school supplies.
Same Day
Frequency of Movements During Free Arrangement
Time Frame: Same Day
Researchers blindly rate how many times participants move an object while freely arranging a box of school supplies.
Same Day
Amount of Space Used During Free Arrangement
Time Frame: Same Day
Researchers blindly rate how much space participants use while freely arranging a box of school supplies (small, medium, or large space).
Same Day
Length of Carpet Arrangement
Time Frame: Same Day
Researchers blindly rate and compare how long (secs) it takes participants to arrange a box of school supplies on a plain versus patterned carpet.
Same Day
Frequency of Movements During Carpet Arrangement
Time Frame: Same Day
Researchers blindly rate and compare how many times participants move an object while arranging a box of school supplies on a plain versus patterned carpet.
Same Day
Frequency of Adjustments During Carpet Arrangement
Time Frame: Same Day
Researchers blindly rate and compare how many times participants adjust the positioning of an object while arranging a box of school supplies on a plain versus patterned carpet.
Same Day
Size of Arrangement According to Sample
Time Frame: Same Day
Researchers blindly rate and compare how accurately participants replicate the size of the arrangement according to a sample picture (smaller than sample, approximate to sample, larger than sample) on a plain versus patterned carpet.
Same Day
Frequency of Checking the Sample
Time Frame: Same Day
Researchers blindly rate and compare how many times participants check the sample picture of the arrangement while organizing a box of school supplies on a plain versus patterned carpet.
Same Day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Gail A Bernstein, MD, University of Minnesota

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

March 1, 2014

Primary Completion (Actual)

March 1, 2015

Study Completion (Actual)

March 1, 2015

Study Registration Dates

First Submitted

August 1, 2016

First Submitted That Met QC Criteria

August 10, 2016

First Posted (Estimate)

August 15, 2016

Study Record Updates

Last Update Posted (Estimate)

August 15, 2016

Last Update Submitted That Met QC Criteria

August 10, 2016

Last Verified

August 1, 2016

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 1403M49006
  • CNS 1338042 (Other Grant/Funding Number: United States National Science Foundation)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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