Adapted Table Tennis for Disabilities
23 de junio de 2026 actualizado por: Kaohsiung Medical University Chung-Ho Memorial Hospital
Health Promotion Through Adapted Table Tennis for Individuals With Disabilities
In recent years, sports participation among individuals with disabilities has increased, driven by medical advancements, growing societal awareness, and improved accessibility.
However, a significant proportion-about 60%-still do not engage in regular physical activity, often due to limited awareness and environmental barriers.
Organizations like the International Paralympic Committee (IPC) have played a key role in promoting disability sports, as evidenced by the growth in Paralympic participation from 400 athletes in 1960 to an expected 4,400 in 2024.
Physical activity offers both physical and psychological benefits for people with disabilities, including improved cardiovascular health, motor function, and emotional well-being.
Although adapted table tennis is a promising, accessible sport for this population, research on its health effects remains limited.
This study aims to evaluate the impact of a 12-week adapted table tennis program on the physical and mental health of individuals with disabilities and to explore its potential as a sustainable health-promotion strategy.
Descripción general del estudio
Estado
Reclutamiento
Condiciones
Intervención / Tratamiento
Descripción detallada
In recent decades, the participation of individuals with disabilities in sports has gradually increased, closely associated with medical advancements, growing societal emphasis on physical well-being, and the expansion of exercise opportunities. According to statistics from the United States Census Bureau, there were approximately 85 million people with disabilities in 2014; however, only around 2 million of them participated in recreational or competitive sports. Despite the growing availability of sports opportunities, about 60% of individuals with disabilities still do not engage in regular physical activity. This indicates the presence of multiple barriers to participation, such as limited awareness about the benefits of exercise and inadequate accessibility of sports facilities.
The International Paralympic Committee (IPC) and various National Governing Bodies (NGBs) have played a crucial role in promoting sports participation among individuals with disabilities by establishing institutionalized competition and training systems that foster the development of sports culture. For example, the number of athletes participating in the Paralympic Games has grown from 400 at the 1960 Rome Paralympics to 4,200 at the 2012 London Paralympics. The 2024 Paris Paralympic Games are expected to host 4,400 athletes, reflecting the rapid growth and increasing recognition of disability sports. This growth not only represents society's greater acceptance of para-sports but also underscores the demand among individuals with disabilities for participation and the potential health benefits associated with such involvement.
The health benefits of physical activity for individuals with disabilities are well-supported by a growing body of research. Exercise has been shown to improve endurance, muscular strength, cardiopulmonary function, and flexibility. It also enhances balance and motor skills. Moreover, physical activity provides significant psychological benefits, including improved self-esteem, body image, self-awareness, and emotional regulation. From a cardiovascular perspective, athletes with disabilities tend to have higher levels of high-density lipoprotein (HDL) cholesterol, lower smoking rates, and a reduced risk of cardiovascular disease. Specific populations, such as individuals with amputations or spinal cord injuries, also benefit from physical activity through improved proprioception, reduced hospitalization rates, lower incidence of pressure ulcers, and decreased infection risk.
Nevertheless, current research on the health benefits of adapted table tennis for individuals with disabilities remains relatively limited. Due to its technical versatility, high adaptability, and low facility requirements, table tennis has emerged as a suitable exercise option for this population. This study will implement a 12-week table tennis training program to assess its impact on the physical and mental health of individuals with disabilities and further evaluate whether this form of exercise can serve as an effective strategy for promoting their overall well-being.
The findings of this study aim to fill the existing research gap regarding the effects of adapted table tennis on individuals with disabilities and provide an empirical foundation for future exercise intervention programs, thereby advancing the promotion and development of regular physical activity among this population.
Tipo de estudio
Intervencionista
Inscripción (Estimado)
40
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
- Nombre: Chia-Ling Lee, MD
- Número de teléfono: 886975357361
- Correo electrónico: cathyleetw@gmail.com
Ubicaciones de estudio
-
-
Taiwan
-
Kaohsiung City, Taiwan, Taiwán, 807
- Reclutamiento
- Kaohsiung Medical University Chung-Ho Memorial Hospital
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Contacto:
- Chia-Ling Lee, MD
- Número de teléfono: 886975357361
- Correo electrónico: cathyleetw@gmail.com
-
-
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
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
No
Descripción
Inclusion Criteria:
- Individuals aged 18 to 75 years who hold a disability identification certificate issued by the Taiwan government and have been assessed by a physician and a professional coach as suitable for participating in adapted table tennis, with a willingness to take part in the study; Participants must respond "No" to all questions in the first section of the Physical Activity Readiness Questionnaire for Everyone (PAR-Q+ 2024 edition) or, if they respond "Yes" to one or more questions in the first section, must respond "No" to all questions in the second section.
Exclusion Criteria:
- Individuals with uncontrolled cardiovascular diseases or relevant neurological history.
- Hearing impairment.
- Cognitive dysfunction.
- Individuals with uncontrolled psychiatric disorders who are unable to comply with the assessments.
- Individuals with color vision deficiencies or visual impairments.
- Pregnant women (self-reported).
- Individuals who have undergone lower limb musculoskeletal surgery or experienced musculoskeletal injuries within the past 6 months.
- Individuals with a history of significant head trauma.
- Individuals unable to comply with the testing schedule.
- Individuals advised by a physician to avoid moderate to high-intensity exercise or those deemed unsuitable for physical activity.
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 |
|---|---|
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Experimental: Adapted table tennis training group
The participants who engage in weekly 2-hour group table tennis sessions for 12 weeks.
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Under the guidance of a professional adapted sports coach, participants in the experimental group will engage in weekly 2-hour group table tennis sessions for 12 weeks.
The sessions will include warm-up exercises, basic table tennis techniques, skill practice, and cool-down stretching exercises.
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Sin intervención: Control group
The participants who only receive regular medical management without exercise training
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Muscle strength
Periodo de tiempo: Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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Static grip strength test
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Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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Volume of Forced Vital Capacity (FVC) in Liters
Periodo de tiempo: Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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FVC is the total volume of air that can be forcefully and completely exhaled after a full inspiration.
It is measured in liters (L) using a digital spirometer.
Higher values indicate greater lung volume and better respiratory capacity.
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Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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6-Minute Walk/Push Test (6MWPT) Distance
Periodo de tiempo: Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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This outcome measures the maximal distance a participant can travel in 6 minutes on a hard, flat surface.
Depending on the participant's ambulatory ability, this was conducted either by walking (6-Minute Walk Test) or by propelling a manual wheelchair (6-Minute Push Test).
The total distance is recorded in meters (m).
Higher values indicate better cardiopulmonary endurance and functional mobility.
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Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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Flexibility
Periodo de tiempo: Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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chair sit-and-reach test
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Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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Waist Circumference in Centimeters
Periodo de tiempo: Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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Waist circumference will be measured using a flexible, non-stretchable anthropometric tape.
The measurement is taken at the midpoint between the lower margin of the last palpable rib and the top of the iliac crest (or at the level of the umbilicus, depending on your exact protocol).
The data will be reported as a continuous variable in centimeters (cm).
This measurement serves as an indicator of central adiposity and body composition changes.
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Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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Total Score on the Generalized Anxiety Disorder 7-Item (GAD-7) Scale
Periodo de tiempo: Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2)
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The GAD-7 is a self-administered questionnaire used to assess the severity of generalized anxiety disorder symptoms.
It consists of 7 items, with each item scored from 0 (not at all) to 3 (nearly every day).
The total aggregated score ranges from 0 to 21.
Higher scores indicate greater severity of anxiety symptoms (Score guidelines: 0-4 minimal, 5-9 mild, 10-14 moderate, 15-21 severe anxiety).
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Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2)
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Bone Mineral Density (BMD) Assessed by Dual-Energy X-ray Absorptiometry in g/cm^2
Periodo de tiempo: Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2)
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Bone mineral density of the whole body (or specific regions such as lumbar spine and femoral neck) will be measured using Dual-Energy X-ray Absorptiometry (DXA).
The outcome is reported in grams per square centimeter (g/cm^2).
Higher values indicate stronger, denser bones and a lower risk of osteopenia or osteoporosis.
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Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2)
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Number of Participants with Abnormal Blood Laboratory Values
Periodo de tiempo: Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2)
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A comprehensive blood panel will be drawn to evaluate general health and physiological safety.
The panel includes metabolic markers (HbA1C), lipid profile (Total cholesterol, Triglycerides, HDL, LDL), renal function and electrolytes (BUN, Cr, uric acid, Na, K, Ca, Mg), liver enzymes (GPT, GOT), complete blood count (CBC), albumin, CRP, and Vitamin D. The outcome is reported as the total number of participants exhibiting clinically significant abnormal values outside the standard laboratory reference ranges.
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Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2)
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Volume of Forced Expiratory Volume in 1 Second (FEV1) in Liters
Periodo de tiempo: Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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FEV1 is the maximal volume of air exhaled in the first second of a forced expiration from a position of full inspiration.
It is measured in liters (L) using a digital spirometer.
Higher values indicate better pulmonary function and airway patency.
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Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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Ratio of FEV1 to FVC (FEV1/FVC)
Periodo de tiempo: Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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This outcome calculates the ratio of Forced Expiratory Volume in 1 Second (FEV1) to Forced Vital Capacity (FVC).
It is expressed as a percentage (%).
It serves as a clinical indicator of airway obstruction, with higher values generally indicating better respiratory mechanics.
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Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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Total Lean Body Mass Assessed by Dual-Energy X-ray Absorptiometry (in kg)
Periodo de tiempo: Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2)
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Total body lean mass (which includes muscle mass and excludes fat and bone mineral content) will be measured using Dual-Energy X-ray Absorptiometry (DXA).
The outcome is reported in kilograms (kg).
Higher values indicate greater muscle mass, reflecting positive structural adaptations to the adapted sports intervention.
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Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2)
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Percentage of Total Body Fat Assessed by Dual-Energy X-ray Absorptiometry
Periodo de tiempo: Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2)
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Total body fat percentage will be measured using Dual-Energy X-ray Absorptiometry (DXA).
The outcome is calculated as fat mass divided by total body mass and reported as a percentage (%).
This metric is used to evaluate changes in body composition and metabolic health.
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Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2)
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Otras medidas de resultado
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Sensory, Motor, and F-wave Latencies of the Median and Ulnar Nerves (in ms)
Periodo de tiempo: Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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This outcome measures the electrophysiological latencies of the bilateral median and ulnar nerves using nerve conduction studies.
The parameters include sensory nerve action potential (SNAP) latency, distal motor latency (DML), and minimum F-wave latency.
All latency measurements are recorded and reported in milliseconds (ms).
Prolonged latencies serve as objective indicators of focal nerve entrapment (such as carpal or cubital tunnel syndrome) or proximal conduction delays.
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Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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Sensory and Motor Nerve Conduction Velocities of the Median and Ulnar Nerves (in m/s)
Periodo de tiempo: Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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This outcome measures both the sensory nerve conduction velocity (SNCV) and motor nerve conduction velocity (MNCV) of the bilateral median and ulnar nerves using nerve conduction studies.
All velocities are recorded and reported in meters per second (m/s).
A decrease in conduction velocity may indicate potential nerve demyelination or early nerve compression associated with wheelchair use or adapted sports.
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Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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Number of Participants with Upper Limb Neuropathy (Median or Ulnar)
Periodo de tiempo: Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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Upper limb nerve conduction studies (NCS) will be performed to assess the presence of median neuropathy (e.g., carpal tunnel syndrome) or ulnar neuropathy.
The outcome is reported as the total number of participants diagnosed with either pathology based on abnormal electrophysiological findings.
This evaluates the neurological safety associated with the wheelchair/adapted sports intervention.
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Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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Number of Participants with Ultrasound-Detected Rotator Cuff Tears
Periodo de tiempo: Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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Musculoskeletal ultrasound of the bilateral shoulders will be performed to assess the presence or absence of rotator cuff tears (full-thickness or partial-thickness).
The outcome is reported as the total number of participants exhibiting this pathology.
This parameter serves to evaluate the musculoskeletal safety and potential overuse injury associated with the intervention.
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Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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Number of Participants with Ultrasound-Detected De Quervain's Tenosynovitis
Periodo de tiempo: Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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Musculoskeletal ultrasound of the bilateral wrists will be performed to assess the presence or absence of De Quervain's tenosynovitis (inflammation of the abductor pollicis longus and extensor pollicis brevis tendons).
The outcome is reported as the total number of participants presenting with this pathology.
This parameter serves to evaluate the musculoskeletal safety of the intervention.
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Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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Compound Muscle Action Potential (CMAP) Amplitude of the Median and Ulnar Nerves (in mV)
Periodo de tiempo: Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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The baseline-to-peak amplitude of the compound muscle action potential for bilateral median and ulnar nerves, measured in millivolts (mV).
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Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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Sensory Nerve Action Potential (SNAP) Amplitude of the Median and Ulnar Nerves
Periodo de tiempo: Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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The baseline-to-peak amplitude of the sensory nerve action potential for bilateral median and ulnar nerves, measured in microvolts
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Pre-intervention (T0), after 12 weeks of intervention (T1), and 6 months after intervention (T2).
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Investigadores
- Silla de estudio: Chia-Ling Lee, MD, Kaohsiung Medical University Chung-Ho Memorial Hospital, Physical and Rehabilitation Medicine Department
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)
8 de julio de 2025
Finalización primaria (Estimado)
30 de junio de 2028
Finalización del estudio (Estimado)
31 de diciembre de 2028
Fechas de registro del estudio
Enviado por primera vez
9 de julio de 2025
Primero enviado que cumplió con los criterios de control de calidad
23 de junio de 2026
Publicado por primera vez (Actual)
26 de junio de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
26 de junio de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
23 de junio de 2026
Última verificación
1 de junio de 2026
Más información
Términos relacionados con este estudio
Palabras clave
Otros números de identificación del estudio
- Para_Tb_PA
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
INDECISO
Descripción del plan IPD
The case population of this study is people with disabilities, who are belong to vulnerable populations.
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. .