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Basketbal Based Motor Cognitive Training Promotes Adolescents' Personal Growth Initiative and Reduces Reliance on AI

6. november 2026 opdateret af: Yunliang Zhang

Basketball-Based Motor Cognitive Training Promotes Adolescents' Personal Growth Initiative and Reduces Reliance on AI: A Randomized Controlled Trial

Objective: To explore whether a 12-week basketball-based cognitive-motor dual-task training (CMDT) improves adolescents' personal growth initiative and functional components of AI dependence, and to examine its effects on critical thinking disposition. Methods: This 12-week randomized controlled trial recruited 106 adolescents aged 18-19 years, who were randomly assigned to either the CMDT group or the control group. The CMDT group received basketball training embedded with cognitive tasks, while the control group participated in conventional basketball training with matched exercise volume. Assessments were conducted at baseline (week 0), mid-intervention (week 6), and post-intervention (week 12) using the Personal Growth Initiative Scale-II (PGIS-II), Critical Thinking Disposition Scale (CTDS), and Conversational AI Dependence Scale (CAIDS-20). A 2 × 3 mixed repeated-measures analysis of variance was adopted to test the main effects of group, time, and group-by-time interaction effects.

Studieoversigt

Status

Ikke rekrutterer endnu

Betingelser

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

106

Fase

  • Ikke anvendelig

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 19 år (Voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Aged 18-19 years
  • No formal diagnosis of neurological or psychiatric disorders; - No musculoskeletal injuries within the past 6 months that would interfere with participation in basketball training
  • No prior systematic participation in any structured cognitive-motor training program
  • Ability to participate fully in the 12-week intervention and all testing sessions

Exclusion Criteria:

  • Currently taking medications that may affect cognitive function
  • Having uncorrected vision or hearing impairments
  • Being unable to understand the Chinese version of the questionnaire or test instructions
  • Missing more than three consecutive training sessions during the intervention period.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Dobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Basketball-Based Motor Cognitive Training

The CMDT group was required to complete both motor and cognitive exercises simultaneously. The training was designed to enhance behavioral and cognitive abilities based on the characteristics of the four dimensions of the PGI. The plan was to stimulate the PGI through various scenarios. For example, the offensive time limit was set at 12 or 10 seconds to train the "readiness for change" dimension. During the training period, the experimental group completed a 12-week training program divided into four phases, with three tasks in each phase. Coaches will distribute the training sessions for the three tasks evenly across each phase. Each training session includes a warm-up and dynamic decision-making phase (10 minutes), combining dribbling with visual search tasks to quickly locate markers or teammates on the court; a cognitive-motor integration training phase (40 minutes), incorporating inhibitory control into offensive and defensive drills-such as sudden change-of-direction commands vi

Placebo komparator: Traditional Basketball Training

Participants engaged in basketball fundamentals and competitive drills (dribbling, passing, shooting, and simple tactical exercises) at the same intensity and frequency, but without incorporating any additional cognitive tasks or conducting structured debriefings, in order to isolate the cognitive training component. Aside from the inclusion of cognitive tasks, the two groups were matched in terms of training content, venue, coach qualifications, and intensity. A standard individual training session consists of a warm-up phase (10 minutes), a training phase (40 minutes), and a cool-down phase (10 minutes). Following basic training principles, the coach focuses on dribbling fundamentals, incorporating various hand movements, speed changes, and directional shifts, and concludes the session with shooting or moves around the basket.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Personal Growth Initiative
Tidsramme: 0week、6week、12week

The Personal Growth Initiative Scale-II consists of 16 items rated on a 6-point Likert scale ranging from 0 (strongly disagree) to 5 (strongly agree). The PGIS-II scale has four subscales: Resource Utilization (3 items, e.g., "When I try to change myself, I seek help"), Intentional Behavior (4 items, e.g., "I seize every opportunity to grow"), Planning (5 items, e.g., "I set realistic goals for the changes I want to make"), and Readiness for Change (4 items, e.g., "When I am ready to make specific changes in myself, I can recognize it") . Subscale scores are calculated by averaging the item scores for that subscale. The total scale score is calculated by averaging the scores of the four subscales. Higher scores indicate higher levels of PGI and its subscales.

0week、6week、12week
Reduces Reliance on AI
Tidsramme: 0week、6week、12week

Dependence on artificial intelligence technology is measured using the Conversational AI Dependence Scale . The scale consists of four dimensions and 20 items: lack of control, withdrawal symptoms, emotional changes, and negative effects. The scale uses a five-point rating scale (1 = strongly disagree, 5 = strongly agree); the higher the total score, the greater the dependence on artificial intelligence technology.

0week、6week、12week

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Critical thinking
Tidsramme: 0week、6week、12week

The Chinese revised version of the Critical Thinking Disposition Scale (CTDS), developed by Sosu (2013) , was used. The scale consists of 11 items and includes two dimensions: critical openness (7 items, measuring an individual's openness and acceptance of new perspectives and feedback from others) and reflective skepticism (4 items, measuring an individual's tendency to question and carefully evaluate information rather than blindly accept it). A 5-point Likert scale was used (1 = strongly disagree, 5 = strongly agree); higher scores indicate stronger critical thinking dispositions.

0week、6week、12week

Samarbejdspartnere og efterforskere

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Sponsor

Publikationer og nyttige links

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Hjælpsomme links

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

10. november 2026

Primær færdiggørelse (Anslået)

2. februar 2027

Studieafslutning (Anslået)

9. februar 2027

Datoer for studieregistrering

Først indsendt

29. oktober 2026

Først indsendt, der opfyldte QC-kriterier

6. november 2026

Først opslået (Faktiske)

12. november 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

12. november 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

6. november 2026

Sidst verificeret

1. november 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • TJUS2026-104

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

JA

IPD-deling Understøttende informationstype

  • ICF

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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