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NCT Number: NCT07557732

Engaging Mental Effort: Process- and Person-Based Reward Experiences, Effort Reinforcement Intervention, and Cascading Effects on Challenging Tasks

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:

1. 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? 2. 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? 3. 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:

1. A matrix completion problem solving task, with options to seek tips for solving problems and options to quit early. 2. A response inhibition task, with options to complete a harder or easier version of the task. 3. A cognitive flexibility task, with options to complete a harder or easier version of the task. 4. A puzzle completion task, with an option to quit early. 5. Answer a set of questions about academic effort 6. Parents will complete a set of questions about how they responded to children's recent successes and failures at school.

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Key information

Age range

9 year–13 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children aged 9.00-13.00 years

Exclusion criteria

  • Known or diagnosed developmental disorder (autism, ADHD, other learning disorders or developmental delays)

Treatment and study plan

Performance Rewards

Behavioral

Participants receive more rewards for fast and accurate task performance and fewer rewards for slow and accurate task performance.

Effort Rewards

Behavioral

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.

Primary outcomes

  1. Cognitive Effort Avoidance - Reinforced Task

    Time frame: Immediately after the intervention

    Relative proportion of Less-Demanding Task Selections after reinforcement (Test - Baseline)

  2. 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)

Secondary outcomes

  1. 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

  2. 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.

Study contacts

Contact information is provided by the study sponsor or research team.

Jesse C Niebaum, PhD

CONTACT

[email protected]

530-752-1011

Yuko Munakata, PhD

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

University of California, Davis

Other

Collaborators

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Registry information

Acronym: RoSE2025

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Apr 29, 2026
Registry last updated
Apr 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.