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Aquatic Therapy Versus Sensory Room Intervention for Sensory-Motor Function in Children With Sensory Processing Disorder (AQUA vs SRI Tr)

9 giugno 2026 aggiornato da: Rana Nabil Hussein Mohamed, MTI University

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

This randomized clinical trial compares the effects of aquatic therapy and conventional sensory room intervention on adaptive neural responses and sensory-motor praxis in children with Monochannel Sensory Processing Disorder. Participants will be randomly assigned to one of the two intervention groups. Outcomes related to sensory processing, sensory-motor praxis, and adaptive responses will be evaluated before and after treatment. The study aims to determine whether aquatic therapy provides additional benefits compared with conventional sensory room intervention in improving sensory integration and functional performance in affected children.

Panoramica dello studio

Stato

Non ancora reclutamento

Intervento / Trattamento

Descrizione dettagliata

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

Tipo di studio

Interventistico

Iscrizione (Stimato)

60

Fase

  • Non applicabile

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Bambino

Accetta volontari sani

No

Descrizione

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.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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.
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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in Total Sensory Systems Score (SPM-2)
Lasso di tempo: Baseline (pre-intervention) and immediately after completion of the intervention period (post-intervention).
Baseline (pre-intervention) and immediately after completion of the intervention period (post-intervention).
Significant improvement in the Total Sensory Systems Score (SPM-2), indicating a shift from monochannel reliance to effective multi-sensory integration.
Lasso di tempo: Baseline (pre-intervention) and immediately after completion of the intervention period (post-intervention).
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.
Baseline (pre-intervention) and immediately after completion of the intervention period (post-intervention).

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

15 giugno 2026

Completamento primario (Stimato)

15 novembre 2026

Completamento dello studio (Stimato)

20 dicembre 2026

Date di iscrizione allo studio

Primo inviato

9 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

9 giugno 2026

Primo Inserito (Effettivo)

15 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

15 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

9 giugno 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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