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Effects of a 12-Week Pickleball Training Program on Cognitive and Motor Skills in Adolescents With Mild Intellectual Disability (PBID-12)

8 de mayo de 2026 actualizado por: Elif Top

From Focus to Function: Effects of a 12-Week Pickleball Training Program on Cognitive and Motor Outcomes in Individuals With Intellectual Disability

This study aims to investigate the effects of a 12-week pickleball training program on cognitive and motor outcomes in adolescents with mild intellectual disability. Pickleball is a low-impact racket sport that combines elements of tennis, badminton, and table tennis, and is considered suitable for promoting both physical and cognitive engagement.

A total of 32 students aged 14-18 years with mild intellectual disability, enrolled in a special education vocational school, will participate in the study. Participants will be assigned to either an intervention group (n = 16) or a control group (n = 16). The intervention group will receive structured pickleball training three times per week for 12 weeks, while the control group will continue their regular educational activities without additional intervention.

Cognitive outcomes will be assessed using standardized computerized tests, including sustained attention (Mackworth Clock Test), visual-spatial memory (Corsi Block Test), selective attention and reaction (Change Detection Test), and working memory (Digit Span Test). Motor outcomes will be evaluated using grip strength, balance assessments, and the Bruininks-Oseretsky Test of Motor Proficiency (BOT-2).

Assessments will be conducted at four time points: baseline (pre-test), mid-intervention (6th or 7th week), post-intervention (week 12), and follow-up (4-6 weeks after completion). The primary aim is to determine whether structured pickleball training improves cognitive performance and motor skills in adolescents with mild intellectual disability.

Findings from this study are expected to contribute to evidence-based physical activity interventions for individuals with intellectual disabilities and to expand the literature on the role of racket sports in cognitive and motor development.

Descripción general del estudio

Estado

Activo, no reclutando

Condiciones

Intervención / Tratamiento

Descripción detallada

This study will be conducted using a quasi-experimental pre-test-post-test control group design to examine the effects of a 12-week pickleball training program on physical and cognitive outcomes in individuals with mild intellectual disability. Participants will be recruited from a special education vocational school and will be aged between 14 and 18 years.

Participants will be assigned to either an experimental group or a control group. The experimental group will participate in a structured pickleball training program for 12 weeks, delivered three times per week. Each session will include two on-court practice sessions and one skill-based training session focusing on fundamental movement and sport-specific skills. Each training session will consist of a 5-minute warm-up, a 40-minute main activity phase, and a 5-minute cool-down period. The control group will continue their regular school-based physical education and daily academic routines without additional intervention.

Outcome assessments will be conducted at four time points: baseline (pre-test), mid-intervention (week 6-7), post-intervention (week 12), and follow-up (4-6 weeks after completion of the intervention). All assessments will be administered by the same research team using standardized protocols to ensure consistency.

Cognitive functions will be evaluated using computer-based tests from the Psychology Experiment Building Language (PEBL) battery. Sustained attention will be assessed using the Mackworth Clock Test, visuospatial working memory using the Corsi Block Test, selective attention and change detection ability using the Change Detection Test, and processing speed and short-term memory using the Digit Span Test.

Motor performance will be assessed using the Bruininks-Oseretsky Test of Motor Proficiency, Second Edition (BOT-2) short form. This standardized assessment evaluates fine motor precision, bilateral coordination, balance, agility, and strength-related motor skills.

In addition, handgrip strength will be measured using a handheld dynamometer, and lower extremity muscular endurance will be assessed using the 30-second sit-to-stand test. Balance performance will also be evaluated through the BOT-2 balance subtests.

All intervention sessions will be adapted to the functional abilities of participants to ensure safety and accessibility. Activities will be delivered by a qualified instructor supported by an assistant instructor, with individualized guidance provided as needed.

Data will be analyzed using appropriate statistical methods based on distribution assumptions. A mixed-design repeated measures ANOVA will be used to examine group-by-time interactions. The level of significance will be set at p < .05.

Tipo de estudio

Intervencionista

Inscripción (Actual)

32

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.

Ubicaciones de estudio

  • Turquía (Türkiye)
    • Burdur
      • Burdur, Burdur, Turquía (Türkiye), 15200
        • Şehit Hakan Aktürk Special Education Vocational School

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

  • Niño
  • Adulto

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  • Having a diagnosis of mild intellectual disability
  • Being enrolled in a special education vocational high school
  • Being between 14 and 18 years of age
  • Having the ability to follow simple verbal instructions
  • Having no additional severe or secondary disability
  • Having no musculoskeletal condition preventing racket use
  • Providing voluntary assent and parental consent

Exclusion Criteria:

  • Refusal to participate in the study at any stage
  • Irregular school attendance during the intervention period
  • Failure to attend pickleball training sessions consistently
  • Presence of a chronic medical condition limiting participation
  • Participation in racket sports within the last 3 months
  • Withdrawal of parental consent during the study

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: Otro
  • Asignación: No aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Pickleball Training Intervention Group

Participants assigned to this arm will participate in a 12-week structured pickleball training program. The intervention will be delivered three times per week under the supervision of a certified physical education specialist and an assistant instructor. Each session will last approximately 45 minutes and will include a standardized structure consisting of a 5-minute warm-up, 40 minutes of pickleball-specific training activities, and a 5-minute cool-down period.

The training content will include fundamental and advanced pickleball skills such as serving, forehand and backhand strokes, volley, dink, lob, smash, drop shot, and basic game strategies. Sessions will be conducted either in the school gymnasium or outdoor court depending on environmental conditions. The intervention aims to improve motor proficiency, balance, strength, and cognitive performance in adolescents with mild intellectual disability.
Conductual: Pickleball Training Intervention Group

A structured 12-week pickleball training intervention will be implemented for adolescents with mild intellectual disability. The program will be delivered three times per week under the supervision of a qualified physical education specialist and an assistant instructor. Each session will last approximately 45 minutes and will follow a standardized structure consisting of a 5-minute warm-up, 40 minutes of skill-based pickleball training, and a 5-minute cool-down period.

The training content will include progressive instruction and practice of fundamental and advanced pickleball skills, including serving, forehand and backhand strokes, volley, dink, lob, smash, drop shot, and basic tactical gameplay. Sessions will be conducted in either an indoor gymnasium or outdoor court depending on weather conditions. The intervention is designed to improve motor proficiency, balance, muscular strength, and cognitive performance in participants with mild intellectual disability.
Comparador activo: Standard Special Education Curriculum
Participants assigned to this arm will continue their regular special education curriculum without participation in any structured physical activity or pickleball-based training program during the study period.
Otro: Standard Special Education Curriculum
Participants in the control group will continue their standard special education curriculum without participation in any structured physical activity or pickleball-based training throughout the study period.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Sustained Attention
Periodo de tiempo: Baseline (Week 0, pre-intervention), Mid-intervention (Week 6-7), Post-intervention (Week 12), Follow-up (4-6 weeks after intervention completion)
Sustained attention will be assessed using the Mackworth Clock Test. Higher scores indicate better sustained attention performance.
Baseline (Week 0, pre-intervention), Mid-intervention (Week 6-7), Post-intervention (Week 12), Follow-up (4-6 weeks after intervention completion)
Visuospatial Working Memory
Periodo de tiempo: Baseline (Week 0, pre-intervention), Mid-intervention (Weeks 6-7), Post-intervention (Week 12), and Follow-up (4-6 weeks after intervention completion)
Visuospatial working memory will be assessed using the Block Test. Higher scores indicate better visuospatial working memory performance.
Baseline (Week 0, pre-intervention), Mid-intervention (Weeks 6-7), Post-intervention (Week 12), and Follow-up (4-6 weeks after intervention completion)
Selective Attention
Periodo de tiempo: Baseline (Week 0, pre-intervention), Mid-intervention (Weeks 6-7), Post-intervention (Week 12), and Follow-up (4-6 weeks after intervention completion)
Selective attention will be assessed using the Change Detection Test. Higher scores indicate better selective attention performance.
Baseline (Week 0, pre-intervention), Mid-intervention (Weeks 6-7), Post-intervention (Week 12), and Follow-up (4-6 weeks after intervention completion)
Working Memory
Periodo de tiempo: Baseline (Week 0, pre-intervention), Mid-intervention (Weeks 6-7), Post-intervention (Week 12), and Follow-up (4-6 weeks after intervention completion)
Working memory will be assessed using the Digit Span Test. Higher scores indicate better working memory performance.
Baseline (Week 0, pre-intervention), Mid-intervention (Weeks 6-7), Post-intervention (Week 12), and Follow-up (4-6 weeks after intervention completion)
Motor Proficiency
Periodo de tiempo: Baseline (Week 0), Mid-intervention (Weeks 6-7), Post-intervention (Week 12), and Follow-up (4-6 weeks after intervention completion)
Motor proficiency will be assessed using the BOT-2 Short Form. Higher scores indicate better motor proficiency.
Baseline (Week 0), Mid-intervention (Weeks 6-7), Post-intervention (Week 12), and Follow-up (4-6 weeks after intervention completion)
Balance
Periodo de tiempo: Baseline (Week 0), Mid-intervention (Weeks 6-7), Post-intervention (Week 12), and Follow-up (4-6 weeks after intervention completion)
Balance performance will be assessed using the balance subtests of the BOT-2. Higher scores indicate better balance performance.
Baseline (Week 0), Mid-intervention (Weeks 6-7), Post-intervention (Week 12), and Follow-up (4-6 weeks after intervention completion)
Hand Grip Strength
Periodo de tiempo: Baseline (Week 0), Mid-intervention (Weeks 6-7), Post-intervention (Week 12), and Follow-up (4-6 weeks after intervention completion)
Hand grip strength will be measured using a hand dynamometer. Higher scores indicate greater grip strength.
Baseline (Week 0), Mid-intervention (Weeks 6-7), Post-intervention (Week 12), and Follow-up (4-6 weeks after intervention completion)
Lower Limb Strength
Periodo de tiempo: Baseline (Week 0), Mid-intervention (Weeks 6-7), Post-intervention (Week 12), and Follow-up (4-6 weeks after intervention completion)
Lower limb strength will be assessed using the 30-second sit-to-stand test. Higher repetition scores indicate greater lower limb strength.
Baseline (Week 0), Mid-intervention (Weeks 6-7), Post-intervention (Week 12), and Follow-up (4-6 weeks after intervention completion)

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Height
Periodo de tiempo: Baseline (Week 0), Mid-intervention (Weeks 6-7), Post-intervention (Week 12), and Follow-up (4-6 weeks after intervention completion)
Height will be measured in centimeters to assess anthropometric characteristics.
Baseline (Week 0), Mid-intervention (Weeks 6-7), Post-intervention (Week 12), and Follow-up (4-6 weeks after intervention completion)
Body Weight
Periodo de tiempo: Baseline (Week 0), Mid-intervention (Weeks 6-7), Post-intervention (Week 12), and Follow-up (4-6 weeks after intervention completion)
Body weight will be measured in kilograms to assess anthropometric characteristics.
Baseline (Week 0), Mid-intervention (Weeks 6-7), Post-intervention (Week 12), and Follow-up (4-6 weeks after intervention completion)
Body Mass Index (BMI)
Periodo de tiempo: Baseline (Week 0), Mid-intervention (Weeks 6-7), Post-intervention (Week 12), and Follow-up (4-6 weeks after intervention completion)
Body mass index (BMI) will be calculated using height and body weight measurements and reported in kg/m² to assess anthropometric characteristics.
Baseline (Week 0), Mid-intervention (Weeks 6-7), Post-intervention (Week 12), and Follow-up (4-6 weeks after intervention completion)

Colaboradores e Investigadores

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

Patrocinador

Elif Top

Colaboradores

Burdur Mehmet Akif Ersoy University

Investigadores

  • Investigador principal: Elif Top, Prof.Dr., Burdur Mehmet Akif Ersoy University, Faculty of Sport Sciences

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Publicaciones Generales

  • Bohannon, R. W. (2019). Hand-grip dynamometry predicts future outcomes in aging adults. Journal of Physical Therapy Science, 31(1), 21-26. https://doi.org/10.1589/jpts.31.21 Boucsein, W. (2012). Electrodermal activity (2nd ed.). Springer. Bruininks RH and Bruininks BD (2005) Bruininks-Oseretsky Test of Motor Proficiency, Second Edition. PsycTESTS Dataset. https://doi.org/10.1037/t14991-000. Casals, M., Jimenez, S., Caparros, T., Gallego, R, M. & Baiget, E. (2023). Scoping review and quality of studies on the epidemiology of pickleball injuries. Apunts Sports Medicine, 58. Casper, Jonathan & Bocarro, Jason & Drake, Nicholas. (2023). Physical Activity Associated with Older Adult Pickleball Participation: A Pilot Study. Recreational Sports Journal. 47. Chien, T. C., & Chen, C. C. (2025). Effects of Pickleball intervention on the self-esteem and symptoms of patients with schizophrenia. Sports, 13(1), 21. Chiles, L. (2025). Pickleball for all: Adaptive sports program to address developmental disabilities (pp. 2-14). Texas Woman's University. Fishman, M., & Hirsch, L. J. (2019). Electroencephalography (EEG) is the non invasive measurement of the brain's electric fields. Current Biology, 29(1), 444-450.

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 (Actual)

9 de febrero de 2026

Finalización primaria (Estimado)

5 de mayo de 2026

Finalización del estudio (Estimado)

1 de junio de 2026

Fechas de registro del estudio

Enviado por primera vez

28 de abril de 2026

Primero enviado que cumplió con los criterios de control de calidad

8 de mayo de 2026

Publicado por primera vez (Actual)

14 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

14 de mayo de 2026

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

8 de mayo de 2026

Última verificación

1 de abril de 2026

Más información

Términos relacionados con este estudio

Palabras clave

Términos MeSH relevantes adicionales

Otros números de identificación del estudio

  • GO2025/2429

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

Individual participant data will not be shared due to ethical considerations and the sensitive nature of the study population, which includes individuals with mild intellectual disability. Data confidentiality and participant privacy will be strictly maintained in accordance with institutional and ethical guidelines. Additionally, data use is limited to the approved scope of the present study.

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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