NCT07746557

Brief Summary

Objective: To investigate the effects of brain endurance training on improving motor skill learning in adolescents with mild mental fatigue. Methods: Fifty-eight adolescents experiencing mild mental fatigue were recruited. A 6-week training program was conducted using a 2 (BET group, control group) × 2 (pre- and post-Stroop task) × 3 (0, 3, 6 weeks) mixed-design experimental design. Assessments included basketball free throws, the Visual Analog Scale (VAS-MF), the 3-minute Psychomotor Vigilance Test (PVT-B), the Borg Rating of Perceived Exertion (RPE) to assess performance before and after a 30-minute Stroop task.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
58

participants targeted

Target at P25-P50 for not_applicable

Timeline
2mo left

Started Aug 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress12%
Aug 2026Sep 2026

First Submitted

Initial submission to the registry

July 25, 2026

Completed
8 days until next milestone

Study Start

First participant enrolled

August 2, 2026

Completed
3 days until next milestone

First Posted

Study publicly available on registry

August 5, 2026

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 13, 2026

Expected
6 days until next milestone

Study Completion

Last participant's last visit for all outcomes

September 19, 2026

Last Updated

August 5, 2026

Status Verified

July 1, 2026

Enrollment Period

1 month

First QC Date

July 25, 2026

Last Update Submit

August 3, 2026

Conditions

Outcome Measures

Primary Outcomes (3)

  • Number of Free Throws Made in Basketball

    From enrollment through Week 3 and then Week 6

  • Number of Free Throws in 1 Minute

    From enrollment through Week 3 and then Week 6

  • Free throws made in 1 minute

    From enrollment through Week 3 and then Week 6

Secondary Outcomes (3)

  • VAS-MF

    From enrollment through Week 3 and then Week 6

  • RPE

    From enrollment through Week 3 and then Week 6

  • At the time of the reaction

    From enrollment through Week 3 and then Week 6

Study Arms (2)

BET

EXPERIMENTAL

During training, the BET group completed a 20-minute 2-back task \[28\]; after a 5-minute break, they performed free-throw-related physical and technical training. The training content, intensity, and workload were identical for both groups, and the presentation timing and intervals of the 2-back task stimuli were adjusted every two weeks \[18\]. During testing, both the BET group and the control group completed 20 free-throw attempts and a 1-minute free-throw test \[29\] before and after the 30-minute Stroop task, and underwent PVT-B, VAS-MF, and RPE assessments.

Behavioral: Motor Skill Learning

Control

EXPERIMENTAL

The BET group and the control group underwent the same physical and technical training related to free throws; the training content, intensity, and workload were identical for both groups. While the BET group performed cognitive tasks, the control group rested in place. The presentation timing and intervals of the 2-back task stimuli were adjusted every two weeks \[18\]. During testing, both the BET group and the control group completed 20 free-throw trials and a 1-minute free-throw test \[29\] before and after the 30-minute Stroop task, and underwent PVT-B, VAS-MF, and RPE assessments.

Behavioral: Motor Skill Learning

Interventions

During training, the BET group completed a 20-minute 2-back task \[28\], followed by a 5-minute break, after which they performed free-throw-related physical and technical training. The presentation timing and intervals of the 2-back task stimuli were adjusted every two weeks \[18\]. During testing, the BET group completed 20 free-throw trials and a 1-minute free-throw test \[29\] before and after the 30-minute Stroop task, and underwent PVT-B, VAS-MF, and RPE assessments.

BET

Eligibility Criteria

Age18 Years - 19 Years
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Participants assessed as having mild mental fatigue using the Mental Fatigue VAS scale
  • No prior experience in learning specific motor skills
  • In good physical health, with no history of central nervous system disorders, musculoskeletal injuries, or mental health conditions

You may not qualify if:

  • Individuals with moderate to severe mental fatigue or no mental fatigue
  • Individuals with moderate to severe mental fatigue or no mental fatigue
  • Individuals with a history of traumatic brain injury, epilepsy, chronic headaches, ADHD, anxiety, or depression - Individuals who have sustained a musculoskeletal injury within the past month and are unable to complete standardized exercise routines
  • Individuals taking medications that affect central nervous system function on a long-term basis, or who have consumed caffeine, energy drinks, or alcohol within 24 hours prior to the experiment - Individuals with persistent sleep disorders
  • Individuals unable to cooperate in completing cognitive endurance training and motor skill tests.Individuals with a history of traumatic brain injury, epilepsy, chronic headaches, ADHD, anxiety, or depression
  • Individuals who have sustained a musculoskeletal injury within the past month and are unable to complete standardized exercise routines
  • Individuals taking medications that affect central nervous system function on a long-term basis, or who have consumed caffeine, energy drinks, or alcohol within 24 hours prior to the experiment
  • Individuals with persistent sleep disorders - Individuals unable to cooperate in completing cognitive endurance training and motor skill tests.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Links

MeSH Terms

Conditions

Mental Fatigue

Condition Hierarchy (Ancestors)

FatigueSigns and SymptomsPathological Conditions, Signs and SymptomsBehavioral SymptomsBehavior

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

July 25, 2026

First Posted

August 5, 2026

Study Start

August 2, 2026

Primary Completion (Estimated)

September 13, 2026

Study Completion (Estimated)

September 19, 2026

Last Updated

August 5, 2026

Record last verified: 2026-07

Data Sharing

IPD Sharing
Will share