- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05296252
Attention and Achievement: A Mind Wandering Investigation
May 17, 2023 updated by: University of Houston
Attention and Achievement (A Subproject Affiliated With the Texas Center for Learning Disabilities or TCLD)
This study assesses the impact of mind-wandering on reading and math.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study assesses the impact of mind-wandering on reading and math.
Specifically 120 middle school student participants will receive descriptive measures (of achievement, attention and related factors including mind-wandering), and will receive a brief (~30 min) lesson in reading and math (order counterbalanced).
Participants will receive a brief pre-test, the lesson, and then a post-test on the reading and math outcomes.
75% of the participants will receive a brief manipulation that sets up the influence of mind-wandering, as well as redirects when probe-caught mind-wandering occurs.
The remaining participants will receive only redirects, and only randomly.
Among participants to receive the mind-wandering manipulation, an equal number will receive this only for reading, only for math, and for both reading and math.
Study Type
Interventional
Enrollment (Actual)
53
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 Contact
- Name: Paul T Cirino, PhD
- Phone Number: 832-842-2002
- Email: pcirino@uh.edu
Study Locations
-
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Texas
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Houston, Texas, United States, 77204-5053
- University of Houston
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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
11 years to 15 years (Child)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- enrollment in schools where we have permission to conduct the study
Exclusion Criteria:
- students known to be enrolled in separate curricula (e.g., life-skills classes)
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: Treatment
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Mind Wandering Intervention
75% of participants will receive proactive and reactive mind-wandering information and redirection.
|
Participants in this condition receive a brief introduction to the potential impact of mind-wandering (before learning, proactive), and are redirected to lesson if "probe-caught" mind-wandering are endorsed (during learning, reactive)
|
Active Comparator: Mind Wandering Comparison
25% of participants will receive only mind-wandering redirection, but only at random times.
|
Participants in this condition receive no introduction, and only redirection, and the redirection is random, not in reaction to mind-wandering
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Investigator Developed Items Derived From Reading Content Being Taught
Time Frame: administered one time immediately following the single reading learning session on day 1
|
Participants will answer multiple choice questions regarding the reading material being taught, and the key index will the raw score number correct.
The investigators call the scale "Sleep and Dreams" (after the content the participant is reading about), and the possible score range will be 0 (min) to 24 (max), with higher scores meaning better comprehension of the material.
|
administered one time immediately following the single reading learning session on day 1
|
Investigator Developed Items Derived From Math Content Being Taught
Time Frame: adminstered one time immediately following the single math learning session on day 1
|
Participants will answer multiple choice questions regarding the math material being taught, and the key index will the raw score number correct.
The investigators call the scale "Circles" (after the content being taught), and the possible score range will be 0 (min) to 24 (max), with higher scores meaning better comprehension of the material.
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adminstered one time immediately following the single math learning session on day 1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Investigator Developed Probe-Caught Mind-Wandering
Time Frame: On 12 occasions interspersed during each of the math and reading learning sessions, on day 1 only.
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During the learning (of the reading and math content), participants are prompted on several occasions as to whether their mind was wandering during the lesson.
This is a single item multiple/choice scale (called Probe-Caught Mind Wandering), with the range being 0 (min) to 12 (max), with lower scores indicating the better outcome (less mind wandering)
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On 12 occasions interspersed during each of the math and reading learning sessions, on day 1 only.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Paul T. Cirino, PhD, University of Houston
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 (Actual)
May 11, 2022
Primary Completion (Actual)
June 15, 2022
Study Completion (Actual)
June 15, 2022
Study Registration Dates
First Submitted
January 25, 2022
First Submitted That Met QC Criteria
March 23, 2022
First Posted (Actual)
March 25, 2022
Study Record Updates
Last Update Posted (Actual)
May 19, 2023
Last Update Submitted That Met QC Criteria
May 17, 2023
Last Verified
May 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- 00000568
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
If another researcher with an approved Institutional Review Board (IRB) protocol wishes to utilize the data for purposes that are non-overlapping with the investigators, they may reach out to the Study PI, who can share de-identified individual data.
IPD Sharing Time Frame
Data will become available after the paper describing the study is published in a peer-reviewed Journal, and will be available for up to 5 years following the termination of the study
IPD Sharing Access Criteria
If another researcher with an approved Institutional Review Board (IRB) protocol wishes to utilize the data for purposes that are non-overlapping with the investigators, they may reach out to the Study PI, who can share de-identified individual data.
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- ICF
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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