Study Results
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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RECRUITING
NA
260 participants
INTERVENTIONAL
2019-08-13
2026-07-31
Brief Summary
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Detailed Description
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After the third testing time point, in the fall of 1st grade, the bottom 1/3 of readers in the sample will be selected to participate in the intervention arm of the study. These students will be randomly placed in one of two arms: business-as-usual, in which children receive no additional instruction; or the reading intervention condition, in which they receive 20 hours of 1:1 reading intervention over 6 weeks. Children in both sub-sample arms are assessed again after tutoring is complete, in the spring of 1st grade.
Neuroimaging through magnetic resonance imaging (MRI) and functional magnetic resonance imaging (fMRI) will occur as part of study participation in conjunction with testing at fall of Kindergarten, fall of 1st grade, and spring of 1st grade time points.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
SINGLE
Study Groups
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Reading Tutoring Intervention
20 hours of one-on-one reading tutoring administered over 6 weeks
Reading Tutoring
20 hours of 1:1 reading tutoring intervention over 6 weeks
Business as Usual
Instruction as usual within schools
No interventions assigned to this group
Interventions
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Reading Tutoring
20 hours of 1:1 reading tutoring intervention over 6 weeks
Eligibility Criteria
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Inclusion Criteria
2. Native English speakers
Exclusion Criteria
2. previous diagnosis of Intellectual Disability;
3. known uncorrectable visual impairment;
4. documented hearing impairment greater than or equal to a 25 decibel (dB) loss;
5. medical contraindication to MRI procedures (e.g., metal devices) - excludes from MRI procedures only;
6. known intelligence quotient (IQ) below 70;
7. a pervasive developmental disorder; and
8. any known neurologic pathology, including epilepsy, spina bifida, cerebral palsy, traumatic brain injury, and brain tumors.
9. Comorbid severe psychiatric disorders will also be excluded, as will those who are taking psychotropic medications, with the exception of stimulant medication for Attention Deficit Hyperactivity Disorder (ADHD). Children who meet criteria for ADHD will be eligible as long as they are not taking psychotropic medications, with the exception of stimulant medication for ADHD.
4 Years
9 Years
ALL
Yes
Sponsors
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Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
NIH
Vanderbilt University
OTHER
Responsible Party
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Laura Cutting
Principal Investigator
Principal Investigators
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Laurie E Cutting, PhD
Role: PRINCIPAL_INVESTIGATOR
Vanderbilt University
Locations
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Vanderbilt University
Nashville, Tennessee, United States
Countries
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Central Contacts
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Lanier P Sachs, M.Ed.
Role: CONTACT
Other Identifiers
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181739
Identifier Type: -
Identifier Source: org_study_id
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