- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07557732
Engaging Mental Effort: Process- and Person-Based Reward Experiences, Effort Reinforcement Intervention, and Cascading Effects on Challenging Tasks (RoSE2025)
Brief Summary: The goal of this clinical trial is to investigate the influences of children's prior experiences with rewards following successes at school and interventions aimed at influencing children's preferences for challenging cognitive tasks.
The main questions this study aims to answer are as follows:
- Does the frequency of process-based rewards (e.g., rewards for working hard) vs. outcomes-based rewards (i.e., rewards for a good grade) predict children's preferences for challenging cognitive tasks?
- Does providing rewards for taking on effortful cognitive tasks increase children's preferences for challenging cognitive tasks more than providing rewards for performing well on cognitive tasks?
- Does receiving rewards for taking on effortful cognitive tasks increase children's challenge-seeking in novel tasks and questionnaires relevant for academic achievement that have not been previously linked with rewards?
Participants will complete the following tasks:
- A matrix completion problem solving task, with options to seek tips for solving problems and options to quit early.
- A response inhibition task, with options to complete a harder or easier version of the task.
- A cognitive flexibility task, with options to complete a harder or easier version of the task.
- A puzzle completion task, with an option to quit early.
- Answer a set of questions about academic effort
- Parents will complete a set of questions about how they responded to children's recent successes and failures at school.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
In Session 1, 9.00 - 13.00-year-olds will complete the Persistence, Effort, Resilience, and Challenge-seeking task with matrix completion problems. Then, participants will be randomly assigned to one of two groups: A group rewarded for selecting a more challenging cognitive task over an easier cognitive task or a group rewarded for performing well regardless of which cognitive task they select to play. Participants will then complete the response inhibition task, with easier or harder options, and the task switching task, with easier or harder options, prior to receiving rewards, while receiving rewards (response inhibition only), and after receiving rewards. Then, participants will answer questions about their task preferences and questions about their academic effort. Parents will complete questionnaires about how they responded to children's recent successes and failures at school and about their efforts in helping children succeed in school.
In Session 2, approximately one week later, participants will complete the response inhibition tasks while receiving rewards according to their respective group assignments. Then, participants will complete the response inhibition task and task-switching task without rewards, an impossible puzzle task, and the Persistence, Effort, Resilience, and Challenge-seeking task. Lastly, participants will answer questions about their academic effort and general preferences for engaging in mental effort. Parents will complete questionnaires about how they responded to children's recent successes and failures at school.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Yuko Munakata, PhD
- Email: ymunakata@ucdavis.edu
Study Contact Backup
- Name: Jesse C Niebaum, PhD
- Phone Number: 530-752-1011
- Email: jcniebaum@ucdavis.edu
Study Locations
-
-
California
-
Davis, California, United States, 95616
- Recruiting
- Center for Mind and Brain
-
Contact:
- Laura Birch
- Phone Number: 530-752-1011
- Email: cmbadmin@ucdavis.edu
-
Contact:
- Email: jniebaum@gmail.com
-
Sub-Investigator:
- Jesse Niebaum, PhD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Children aged 9.00-13.00 years
Exclusion Criteria:
- Known or diagnosed developmental disorder (autism, ADHD, other learning disorders or developmental delays)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Effort-based Reward Contingency
Great rewards are offered for children who repeatedly decide to complete a more difficult response inhibition task.
|
Participants receive more rewards for choosing to complete the more difficult task and responding accurately and fewer rewards for choosing to complete the less difficult task and responding accurately.
|
|
Experimental: Performance-based Reward Contingency
Rewards are provided for children who perform quickly and accurately, regardless of which response inhibition task option they select to play.
|
Participants receive more rewards for fast and accurate task performance and fewer rewards for slow and accurate task performance.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cognitive Effort Avoidance - Reinforced Task
Time Frame: Immediately after the intervention
|
Relative proportion of Less-Demanding Task Selections after reinforcement (Test - Baseline)
|
Immediately after the intervention
|
|
Cognitive Effort Avoidance - Novel Task
Time Frame: Immediately after the intervention and primary outcome 1
|
Relative proportion of less-demanding task selections from the novel task after reinforcement (Test - Baseline)
|
Immediately after the intervention and primary outcome 1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Challenge-Seeking
Time Frame: Immediately after the follow-up intervention dose
|
Relative change from Session 1 Baseline to Session 2 test (1-week later) in overall challenge-seeking composite metric from the Performance, Effort, Resilience, and Challenge-seeking task
|
Immediately after the follow-up intervention dose
|
|
Persistence on Impossible Puzzles
Time Frame: Immediately after the follow-up intervention dose and secondary outcome measure 1.
|
Time spent persisting on impossible puzzles prior to response deadline or skipping the puzzle problem.
|
Immediately after the follow-up intervention dose and secondary outcome measure 1.
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Director: Jesse Niebaum, PhD, University of California, Davis
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 1518244-A
- R01HD086184 (U.S. NIH Grant/Contract)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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