- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01518738
Attention Training
June 3, 2014 updated by: University of Wisconsin, Madison
The purpose of this study is to understand whether attention training is effective in moderating mind wandering.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Our subjective worlds are built from those things in our internal and external environments that capture our attention.
Environments can be ambiguous with respect to which objects are most important for our attention, and the characteristics of stimuli that allow them to dominate attention are thus of great interest.
Self-relevant objects, such as internally generated experience (e.g.
thought), may receive substantial attention, but research on this dimension has been hampered by the difficulty of measuring such objects experimentally.
The proposed study seeks to make headway in this area using several behavioral (accuracy, response time, response pattern) measures, with the hypothesis that internally generated experience will vie for attention in a way reflected by behavior.
Such research will extend previous work the investigators' lab has done studying stimulus parameters that influence attention, and as a whole may present a more complete picture of how objects and attention interact to shape our worlds.
Study Type
Interventional
Enrollment (Actual)
94
Phase
- Not Applicable
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
-
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Wisconsin
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Madison, Wisconsin, United States, 53706
- University of Wisconsin Brogden Psychology Building
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-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Exclusion Criteria:
- Non-English speakers
Inclusion Criteria:
- Must be able to use a computer
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
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: no training
|
|
Experimental: breath attention training
|
4 week training
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Active Comparator: working memory attention training
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4 week training
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
change in mind wandering frequency after intervention
Time Frame: before intervention and up to 100 weeks later
|
mind wandering will be assessed with self-report to intermittent queries such as "just now, was your attention on the present task or unrelated concerns?"
Frequency of endorsement will serve as a measure of frequency of mind wandering (ranging in units from 0 - 100% of the time).
|
before intervention and up to 100 weeks later
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Richard Davidson, PhD, University Wisconsin Madison
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
February 1, 2012
Primary Completion (Actual)
November 1, 2012
Study Completion (Actual)
November 1, 2012
Study Registration Dates
First Submitted
January 13, 2012
First Submitted That Met QC Criteria
January 23, 2012
First Posted (Estimate)
January 26, 2012
Study Record Updates
Last Update Posted (Estimate)
June 5, 2014
Last Update Submitted That Met QC Criteria
June 3, 2014
Last Verified
June 1, 2014
More Information
Terms related to this study
Other Study ID Numbers
- SE-2011-0123
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.
Clinical Trials on Attention
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Jeroen Bosch ZiekenhuisCompletedSustained Selective Attention | Divided AttentionNetherlands
-
National Taiwan University HospitalUnknownAttention on Posture | Attention on SuprapostureTaiwan
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Cingulate TherapeuticsRecruitingPhase 3 Efficacy and Safety Laboratory Classroom Study in Pediatrics (6-12) With ADHD Using CTx-1301ADHD | Attention Deficit Hyperactivity Disorder | Attention Deficit Disorder With Hyperactivity | ADHD - Combined Type | Attention Deficit Hyperactivity Disorder Combined | Attention Deficit Hyper Activity | Attention-deficit HyperactivityUnited States
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Ornit CohenUnknownAttention Deficit Hyperactivity Disorder | Attention Deficit Disorder With Hyperactivity | Attention Deficit Disorder | Attention Deficit Disorders With Hyperactivity | Attention Deficit Hyperactivity DisordersIsrael
-
University of PennsylvaniaNational Institutes of Health (NIH)TerminatedAttention Deficit Hyperactivity Disorder | Attention Deficit Disorder | Working MemoryUnited States
-
National Institute on Alcohol Abuse and Alcoholism...TerminatedAttention Deficit Disorder | Attention Deficit Hyerpactivity DisorderUnited States
-
Cingulate TherapeuticsPremier Research Group plcActive, not recruitingADHD | Attention Deficit Hyperactivity Disorder | ADHD - Combined Type | Attention Deficit Hyperactivity Disorder Combined | Attention Deficit Hyper Activity | Attention-deficit HyperactivityUnited States
-
Institut de Recherche Biomedicale des ArmeesUniversity of Paris 5 - Rene Descartes; Hotel Dieu de France HospitalRecruiting
-
Virginia Commonwealth UniversityWithdrawnAttention Fatigue, Attention Restoration
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Barcelona Institute for Global HealthRecercaixa; Centre de Recerca per a l'Educació Científica i Matemàtica (CRECIM) and other collaboratorsCompletedRisk Behavior | Attention Impaired | Risk-Taking | Social Preferences | Decision Making | AttentionSpain
Clinical Trials on breath attention training
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Technical University of MunichGerman Research Foundation; Studienstiftung des deutschen VolkesRecruitingExperimental Pain in Healthy Human SubjectsGermany
-
Mclean HospitalTerminatedDepression | Attention Training | Symptoms, Cognitive | Symptoms, Affective | Symptoms, BehavioralUnited States
-
King's College LondonNetherlands Organisation for Scientific ResearchUnknownAnorexia NervosaUnited Kingdom
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University of California, San FranciscoCompleted
-
Hospital de Clinicas de Porto AlegreCompleted
-
Palo Alto UniversityRecruiting
-
University of California, San FranciscoAlliance for Decision EducationCompletedHealthy AdolescentsUnited States
-
Tel Aviv UniversityCompleted
-
The University of Hong KongUnknownDevelopmental Coordination DisorderHong Kong