Aquatic Therapy Versus Sensory Room Intervention for Sensory-Motor Function in Children With Sensory Processing Disorder (AQUA vs SRI Tr)
Comparative Impact of Aquatic Therapy and Conventional Sensory Room Intervention on Adaptive Neural Responses and Sensory-Motor Praxis in Children With Monochannel Sensory Processing Disorder: A Randomized Clinical Trial
Przegląd badań
Status
Status
Warunki
Warunki
Interwencja / Leczenie
Interwencja / Leczenie
Szczegółowy opis
Monochannel sensory processing disorder refers to a condition where a child tends to rely heavily on a single sensory channel-usually visual, auditory, or tactile-while ignoring or underutilizing others. This limited sensory integration can negatively affect the child's ability to interact with the environment, learn effectively, and develop age-appropriate motor and cognitive skills. Children with monochannel processing often struggle with transitions, emotional regulation, and tasks requiring multi-sensory coordination. Aquatic therapy is a powerful therapeutic intervention that uses the unique properties of water-such as buoyancy, hydrostatic pressure, resistance, and temperature-to create a multisensory environment that enhances motor control, body awareness, attention, and sensory integration. These qualities make it particularly effective for children with sensory processing difficulties. Aquatic therapy supports sensory processing by stimulating multiple sensory systems simultaneously. For example, the pressure of the water provides deep proprioceptive input, movement through water enhances vestibular feedback, and water temperature activates tactile receptors. This simultaneous multisensory input can help children shift from single-sense reliance to more integrated, adaptive responses.
60 children diagnosed with monochannel sensory processing disorder, aged 4-8 years (both sexes) Two equal groups: Intervention group (Aquatic therapy) and Control group (Sensory room therapy), 30 children each.
Two equal groups: Intervention group (Aquatic therapy) and Control group (Sensory room therapy), 30 children each.
Inclusion Criteria:
Children aged 4-8 years with a confirmed diagnosis of monochannel sensory processing disorder.
Exclusion Criteria:
Subjects will be excluded from the study if they meet any of the following conditions:
- Medical Instability: Any acute illness, fever, or infectious diseases (e.g., ear infections or open wounds) that contraindicate pool therapy.
- Neurological Risks: Children with uncontrolled seizures or epilepsy that poses a safety risk in an aquatic environment.
- Severe Phobia: Extreme fear of water (hydrophobia) that prevents active participation in aquatic exercises.
- Recent Surgery: Any recent surgical interventions (orthopedic or neurological) that have not yet reached full clinical clearance for physical activity.
- Incontinence: Severe lack of bowel or bladder control unless specific medical swim diapers are utilized according to facility policy.
Measuring Tools:
To evaluate the transition from monochannel reliance to multi-sensory integration, the following standardized tools will be utilized:
- Sensory Processing Measure (SPM-2): Used to assess multi-sensory integration across different environments (home and school) and provide a total sensory systems score.
- Evaluation of Ayres Sensory Integration (EASI): Employed to measure adaptive neural responses, sensory perception, and motor planning (praxis).
- Sensory Integration and Praxis Tests (SIPT): A comprehensive diagnostic battery used to evaluate the relationship between sensory processing and motor behavior in depth.
Procedure (brief outline):
1. Evaluation procedures: Pre-treatment assessment of sensory integration and processing abilities to each group.
Group A: Aquatic Therapy Intervention (Experimental Group) The aquatic program utilizes the physical properties of water (buoyancy, hydrostatic pressure, and resistance) to provide multi-sensory input.
Group B: Conventional Sensory Room Therapy (Control Group) This group receives land-based sensory integration therapy in a standard clinical setting.
- Primary Outcome: Significant improvement in the Total Sensory Systems Score (SPM-2), indicating a shift from monochannel reliance to effective multi-sensory integration.
- Secondary Outcomes: Enhanced Adaptive Neural Responses and sensory perception as measured by EASI, and improved Sensory-Motor Praxis and coordination as quantified by SIPT
Typ studiów
Typ studiów
Zapisy (Szacowany)
Zapisy
Faza
Faza
- Nie dotyczy
Kryteria uczestnictwa
Kryteria kwalifikacji
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dziecko
Akceptuje zdrowych ochotników
Opis
Inclusion Criteria:
- Children aged 4-8 years with a confirmed diagnosis of monochannel sensory processing disorder.
Exclusion Criteria:
- Medical Instability: Any acute illness, fever, or infectious diseases (e.g., ear infections or open wounds) that contraindicate pool therapy.
- Neurological Risks: Children with uncontrolled seizures or epilepsy that poses a safety risk in an aquatic environment.
- Severe Phobia: Extreme fear of water (hydrophobia) that prevents active participation in aquatic exercises.
- Recent Surgery: Any recent surgical interventions (orthopedic or neurological) that have not yet reached full clinical clearance for physical activity.
- Incontinence: Severe lack of bowel or bladder control unless specific medical swim diapers are utilized according to facility policy.
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Brak (otwarta etykieta)
Liczba ramion
Broń i interwencje
Grupa uczestników / ArmGrupa uczestników / Arm |
Interwencja / LeczenieInterwencja / Leczenie |
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Eksperymentalny: Aquatic Therapy Group
Participants will receive aquatic therapy sessions as the sole intervention.
The program aims to improve motor function, balance, muscle tone regulation, and upper limb coordination in children with spastic cerebral palsy.
Outcomes will be assessed before and after the intervention period.
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Participants will receive aquatic therapy sessions conducted in a therapeutic pool under the supervision of a licensed physical therapist.
The program will focus on improving sensory-motor integration, postural control, balance, muscle tone regulation, and functional motor skills in children with sensory processing disorder.
Sessions will be delivered multiple times per week over a specified intervention period, with individualized exercises adapted to each child's abilities and therapeutic goals.
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Co mierzy badanie?
Podstawowe miary wyniku
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Change in Total Sensory Systems Score (SPM-2)
Ramy czasowe: Baseline (pre-intervention) and immediately after completion of the intervention period (post-intervention).
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Baseline (pre-intervention) and immediately after completion of the intervention period (post-intervention).
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Significant improvement in the Total Sensory Systems Score (SPM-2), indicating a shift from monochannel reliance to effective multi-sensory integration.
Ramy czasowe: Baseline (pre-intervention) and immediately after completion of the intervention period (post-intervention).
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The primary outcome will be measured using the Sensory Processing Measure-2 (SPM-2).
The Total Sensory Systems Score will be assessed to evaluate changes in sensory integration abilities, specifically the shift from monochannel sensory processing to more effective multisensory integration.
Assessments will be conducted at baseline and after completion of the intervention period.
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Baseline (pre-intervention) and immediately after completion of the intervention period (post-intervention).
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Współpracownicy i badacze
Sponsor
Sponsor
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Szacowany)
Rozpoczęcie studiów
Zakończenie podstawowe (Szacowany)
Zakończenie podstawowe
Ukończenie studiów (Szacowany)
Ukończenie studiów
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Pierwszy wysłany
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia wysłana aktualizacja
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
Inne numery identyfikacyjne badania
- RE/2111/MTI.PT/2605121
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
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