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

6 de noviembre de 2026 actualizado por: 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.

Descripción general del estudio

Estado

Aún no reclutando

Condiciones

Intervención / Tratamiento

Tipo de estudio

Intervencionista

Inscripción (Estimado)

106

Fase

  • No aplica

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años a 19 años (Adulto)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

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.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Doble

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: 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

Comparador de placebos: 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.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Personal Growth Initiative
Periodo de tiempo: 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
Periodo de tiempo: 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

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Critical thinking
Periodo de tiempo: 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

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Publicaciones y enlaces útiles

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Enlaces Útiles

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

10 de noviembre de 2026

Finalización primaria (Estimado)

2 de febrero de 2027

Finalización del estudio (Estimado)

9 de febrero de 2027

Fechas de registro del estudio

Enviado por primera vez

29 de octubre de 2026

Primero enviado que cumplió con los criterios de control de calidad

6 de noviembre de 2026

Publicado por primera vez (Actual)

12 de noviembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

12 de noviembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

6 de noviembre de 2026

Última verificación

1 de noviembre de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • TJUS2026-104

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

SÍ

Tipo de información de apoyo para compartir IPD

  • CIF

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .