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OPTIMAL Motor Learning in Table Tennis: A fNIRS Study

27 de octubre de 2026 actualizado por: Hui-Ting Shih, National Yang Ming Chiao Tung University

Does the OPTIMAL Theory Enhance Motor Learning and Cognitive and Sensorimotor Area Cortical Activation? A Theoretical Mechanism Validation in Young, Older Adults, and Cognitively Impaired Older Adults Novice Table Tennis Players

This study investigates how OPTIMAL theory influences table tennis backhand learning in young, healthy older, and mild cognitively impaired older adults. Meanwhile, we investigate the neural mechanisms of motor skill acquisition across different ages. This study utilizes functional near-infrared spectroscopy (fNIRS) to monitor brain activity. Beyond immediate performance, the research focuses on Retention (sustained skill over time) and Transfer (application to novel tasks) as critical indicators of true motor learning. To ensure objective results, a double-blind design is employed, where both participants and data analysts remain blinded to group assignments during behavioral and fNIRS data processing to minimize bias.

Descripción general del estudio

Tipo de estudio

Intervencionista

Inscripción (Estimado)

90

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

      • Taipei, Taiwán
        • National Yang Ming Chiao Tung University
        • Contacto:

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 80 años (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Todos

Descripción

Healthy young adults are aged between 18 and 30 years, while healthy older adults and older adults with mild cognitive impairment (MCI) are aged between 65 and 80 years. Regarding cognitive criteria, healthy young adults and healthy older adults must score 24 or higher on the Mini-Mental State Examination (MMSE). Older adults with MCI must further meet the following diagnostic criteria for MCI:

  1. Subjective cognitive decline: The participants themselves or their family members/primary caregivers report a decline in memory or cognitive function.
  2. Objective cognitive impairment: The education-adjusted score on the Taiwanese version of the Montreal Cognitive Assessment (MoCA-T) is between 20 and 23. One point is added to the total MoCA-T score for individuals with less than 12 years of education. Considering the heterogeneity in education levels among Taiwan's older generation, if a participant has 6 or fewer years of education (elementary school or below) or is illiterate, the Chinese version of the Montreal Cognitive Assessment Basic (MoCA-B) will be administered as a supplement. This is to reduce false-positive interference on the visuospatial and executive function subtests caused by a low educational level.
  3. Preserved activities of daily living: The score on the Compensatory Instrumental Activities of Daily Living (IADL-C) scale ranges from 1.34 to 3.06, indicating that the participant possesses the ability to live independently and has not reached the level of dementia.

In addition to the age and cognitive requirements, participants across all three groups must meet the following inclusion criteria:

  1. Right-handed, with an Edinburgh Handedness Inventory (EHI) score > 40;
  2. Table tennis beginners who have never received professional table tennis instruction;
  3. Played table tennis less than once a month in the past year;
  4. Normal hearing and normal or corrected-to-normal vision.

Exclusion criteria include:

  1. Over 3 years of experience in other racket sports;
  2. A history of neurological or psychiatric disorders;
  3. Any musculoskeletal system diseases that might interfere with the experiment;
  4. Unstable cardiopulmonary function rendering them unsuitable for moderate-intensity aerobic exercise;
  5. Taking medications that affect the central nervous system or blood oxygen signals, such as potent sedative-hypnotics, antiepileptic drugs, or antipsychotic medications.

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: Ciencia básica
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Doble

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Young Adults - OPTIMAL

OPTIMAL theory-based instruction

Dose: 15 blocks of practice, with each block consisting of 30 table tennis backhand strokes (Total: 450 trials).

Description: The intervention integrates three components: (1) Autonomy Support (AS): Participants choose the color of the table tennis balls. (2) Enhanced Expectancy (EE): A visual illusion is used where the target is surrounded by smaller circles, making the target appear larger to boost confidence. (3) External Focus (EF): Instructions direct attention toward the target rather than limb movements.

Comparador activo: Young Adults - Control

Conventional instruction

Dose: Same as Experimental group (15 blocks x 30 trials; Total: 450 trials).

Description: (1) No choice is provided (Yoked control). (2) A visual illusion is used where the target is surrounded by larger circles, making the target appear smaller. (3) Instructions focus on body mechanics, such as elbow position and swing path (Internal Focus).

Experimental: Older Adults - OPTIMAL

OPTIMAL theory-based instruction

Dose: 15 blocks of practice, with each block consisting of 30 table tennis backhand strokes (Total: 450 trials).

Description: The intervention integrates three components: (1) Autonomy Support (AS): Participants choose the color of the table tennis balls. (2) Enhanced Expectancy (EE): A visual illusion is used where the target is surrounded by smaller circles, making the target appear larger to boost confidence. (3) External Focus (EF): Instructions direct attention toward the target rather than limb movements.

Comparador activo: Older Adults - Control

Conventional instruction

Dose: Same as Experimental group (15 blocks x 30 trials; Total: 450 trials).

Description: (1) No choice is provided (Yoked control). (2) A visual illusion is used where the target is surrounded by larger circles, making the target appear smaller. (3) Instructions focus on body mechanics, such as elbow position and swing path (Internal Focus).

Experimental: MCI Older Adults - OPTIMAL

OPTIMAL theory-based instruction

Dose: 15 blocks of practice, with each block consisting of 30 table tennis backhand strokes (Total: 450 trials).

Description: The intervention integrates three components: (1) Autonomy Support (AS): Participants choose the color of the table tennis balls. (2) Enhanced Expectancy (EE): A visual illusion is used where the target is surrounded by smaller circles, making the target appear larger to boost confidence. (3) External Focus (EF): Instructions direct attention toward the target rather than limb movements.

Comparador activo: MCI Older Adults - Control

Conventional instruction

Dose: Same as Experimental group (15 blocks x 30 trials; Total: 450 trials).

Description: (1) No choice is provided (Yoked control). (2) A visual illusion is used where the target is surrounded by larger circles, making the target appear smaller. (3) Instructions focus on body mechanics, such as elbow position and swing path (Internal Focus).

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Motor Performance (Accuracy Score)
Periodo de tiempo: Day 1 Pre-test: before practice (3 blocks) Acquisition: during practice (15 blocks) Post-test: immediately after practice (3 blocks) Day 2 Retention test: at least 24 hours after Day 1 (3 blocks) Transfer test: at least 24 hours after Day 1 (3 blocks)

Accuracy is measured with a target-centered scoring system on a 0-7 scale per ball; higher scores indicate better accuracy.

7 pts: Hit target (10 cm diameter).

6 pts: Hit zone (20 cm).

5 pts: Hit zone (30 cm).

4 pts: Hit zone (40 cm).

3 pts: Hit zone (50 cm).

2 pts: Hit opposite table surface but missed target zones.

1 pt: Ball was hit but missed the opposite table.

0 pts: Failed to hit the ball.

The performance is presented by blocks. Each block contains 30 balls. The average score of each block is calculated.

Day 1 Pre-test: before practice (3 blocks) Acquisition: during practice (15 blocks) Post-test: immediately after practice (3 blocks) Day 2 Retention test: at least 24 hours after Day 1 (3 blocks) Transfer test: at least 24 hours after Day 1 (3 blocks)

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Prefrontal Cortex (DLPFC) Activation
Periodo de tiempo: Day 1 Pre-test: before practice (3 blocks) Acquisition: during practice (15 blocks) Post-test: immediately after practice (3 blocks) Day 2 Retention test: at least 24 hours after Day 1 (3 blocks) Transfer test: at least 24 hours after Day 1 (3 blocks)

Change in oxygenated hemoglobin (HbO) concentration (μM) in the bilateral dorsolateral prefrontal cortex (DLPFC), measured using functional near-infrared spectroscopy (fNIRS) during table tennis backhand task blocks.

Day 1 Pre-test: before practice (3 blocks) Acquisition: during practice (15 blocks) Post-test: immediately after practice (3 blocks) Day 2 Retention test: at least 24 hours after Day 1 (3 blocks) Transfer test: at least 24 hours after Day 1 (3 blocks)
Premotor Cortex (PMC) Activation
Periodo de tiempo: Day 1 Pre-test: before practice (3 blocks) Acquisition: during practice (15 blocks) Post-test: immediately after practice (3 blocks) Day 2 Retention test: at least 24 hours after Day 1 (3 blocks) Transfer test: at least 24 hours after Day 1 (3 blocks)

Change in oxygenated hemoglobin (HbO) concentration (μM) in the bilateral premotor cortex (PMC), measured using functional near-infrared spectroscopy (fNIRS) during table tennis backhand task blocks.

Day 1 Pre-test: before practice (3 blocks) Acquisition: during practice (15 blocks) Post-test: immediately after practice (3 blocks) Day 2 Retention test: at least 24 hours after Day 1 (3 blocks) Transfer test: at least 24 hours after Day 1 (3 blocks)
Supplementary Motor Area (SMA) Activation
Periodo de tiempo: Day 1 Pre-test: before practice (3 blocks) Acquisition: during practice (15 blocks) Post-test: immediately after practice (3 blocks) Day 2 Retention test: at least 24 hours after Day 1 (3 blocks) Transfer test: at least 24 hours after Day 1 (3 blocks)

Change in oxygenated hemoglobin (HbO) concentration (μM) in the supplementary motor area (SMA), measured using functional near-infrared spectroscopy (fNIRS) during table tennis backhand task blocks.

Day 1 Pre-test: before practice (3 blocks) Acquisition: during practice (15 blocks) Post-test: immediately after practice (3 blocks) Day 2 Retention test: at least 24 hours after Day 1 (3 blocks) Transfer test: at least 24 hours after Day 1 (3 blocks)
Sensorimotor Cortex (SMC) Activation
Periodo de tiempo: Day 1 Pre-test: before practice (3 blocks) Acquisition: during practice (15 blocks) Post-test: immediately after practice (3 blocks) Day 2 Retention test: at least 24 hours after Day 1 (3 blocks) Transfer test: at least 24 hours after Day 1 (3 blocks)

Change in oxygenated hemoglobin (HbO) concentration (μM) in the sensorimotor cortex (SMC), measured using functional near-infrared spectroscopy (fNIRS) during table tennis backhand task blocks.

Day 1 Pre-test: before practice (3 blocks) Acquisition: during practice (15 blocks) Post-test: immediately after practice (3 blocks) Day 2 Retention test: at least 24 hours after Day 1 (3 blocks) Transfer test: at least 24 hours after Day 1 (3 blocks)
Self-Efficacy (General Self-Efficacy Scale, GSES)
Periodo de tiempo: Day 1 Immediately after Pre-test

Self-efficacy is measured with the General Self-Efficacy Scale (GSES), a 10-item self-report scale.

Each item is rated from 1 (not at all true) to 4 (exactly true), giving a total score of 10 to 40; higher scores indicate higher self-efficacy.

Day 1 Immediately after Pre-test

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Manipulation Check
Periodo de tiempo: Day 1 After Post-test Day 2 After Transfer test

A questionnaire verifying whether participants perceived the assigned experimental manipulations (autonomy support, enhanced expectancies, and attentional focus). It consists of 19 items rated mainly on 0-10 scales (items 10-11 on a 0-100% scale); higher scores indicate stronger agreement or greater perception of the corresponding construct.

Day 1 After Post-test Day 2 After Transfer test

Colaboradores e Investigadores

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

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)

1 de noviembre de 2026

Finalización primaria (Estimado)

31 de agosto de 2028

Finalización del estudio (Estimado)

31 de octubre de 2028

Fechas de registro del estudio

Enviado por primera vez

8 de octubre de 2026

Primero enviado que cumplió con los criterios de control de calidad

27 de octubre de 2026

Publicado por primera vez (Actual)

3 de noviembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

3 de noviembre de 2026

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

27 de octubre de 2026

Última verificación

1 de octubre de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

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. .

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