The Effect of Brain Endurance Training on Motor Skill Learning in Adolescents With Mild Mental Fatigue
2026년 8월 3일 업데이트: Yunliang Zhang
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.
연구 개요
상태
상태
아직 모집하지 않음
정황
정황
개입 / 치료
개입 / 치료
연구 유형
연구 유형
중재적
등록 (추정된)
등록
58
단계
단계
- 해당 없음
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 연락처
연구 연락처
- 이름: Yunliang ZHANG
- 전화번호: +8613920900801
- 이메일: yunliangzhang@126.com
참여기준
연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.
자격 기준
자격 기준
공부할 수 있는 나이
- 성인
건강한 자원 봉사자를 받아들입니다
아니
설명
Inclusion Criteria:
- 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
Exclusion Criteria:
- 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.
공부 계획
이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 더블
팔의 수
2
무기와 개입
참가자 그룹 / 팔참가자 그룹 / 팔 |
개입 / 치료개입 / 치료 |
|---|---|
|
실험적: BET
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.
|
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.
The BET group and the control group underwent 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.
During testing, the control group completed a 20-free-throw test 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.
|
|
실험적: Control
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.
|
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.
The BET group and the control group underwent 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.
During testing, the control group completed a 20-free-throw test 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.
|
연구는 무엇을 측정합니까?
주요 결과 측정
주요 결과 측정
결과 측정 |
기간 |
|---|---|
|
Number of Free Throws Made in Basketball
기간: From enrollment through Week 3 and then Week 6
|
From enrollment through Week 3 and then Week 6
|
|
Number of Free Throws in 1 Minute
기간: From enrollment through Week 3 and then Week 6
|
From enrollment through Week 3 and then Week 6
|
|
Free throws made in 1 minute
기간: From enrollment through Week 3 and then Week 6
|
From enrollment through Week 3 and then Week 6
|
2차 결과 측정
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
VAS-MF
기간: From enrollment through Week 3 and then Week 6
|
The 10cm VAS-MF was used to assess the degree of mental fatigue.
The scale consists of an unmarked horizontal line, with the left end (0 = not at all fatigued) and the right end (10 = completely fatigued) representing the lowest and highest states of this dimension, respectively.
Participants are instructed by the examiner to draw a vertical line on the scale that reflects their immediate feelings.
A quantitative score is derived by measuring the physical distance (0-10 cm) from the left end of the scale to the marked point.
|
From enrollment through Week 3 and then Week 6
|
|
RPE
기간: From enrollment through Week 3 and then Week 6
|
The Borg Rate of Perceived Exertion (RPE) scale assesses perceived exertion (0-10); participants indicate their perceived exertion level using their fingers.
|
From enrollment through Week 3 and then Week 6
|
|
At the time of the reaction
기간: From enrollment through Week 3 and then Week 6
|
All cognitive tasks were conducted using E-Prime 3.0 software.
During the 3-minute PVT-B reaction time test, a visual stimulus lasting 1-8 seconds was first presented in the center of the computer screen; participants were instructed to press the "space" key as quickly as possible to respond, after which the screen went blank for 500 ms before proceeding to the next cycle.
|
From enrollment through Week 3 and then Week 6
|
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간행물 및 유용한 링크
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유용한 링크
연구 기록 날짜
이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.
연구 주요 날짜
연구 시작 (추정된)
연구 시작
2026년 8월 2일
기본 완료 (추정된)
기본 완료
2026년 9월 13일
연구 완료 (추정된)
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연구 등록 날짜
최초 제출
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처음 게시됨 (실제)
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마지막 업데이트 게시됨 (실제)
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마지막으로 확인됨
마지막으로 확인됨
2026년 7월 1일
추가 정보
이 연구와 관련된 용어
기타 연구 ID 번호
기타 연구 ID 번호
- TJUS2025-134
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
예
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
아니
미국 FDA 규제 기기 제품 연구
아니
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .