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Not yet recruiting NCT07646951

Aquatic Therapy Versus Sensory Room Intervention for Sensory-Motor Function in Children With Sensory Processing Disorder

No phase Interventional Neuro Developmental Delay Sensory Disorders

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Aquatic Therapy.
Who it may be relevant to
Registry conditions: Neuro Developmental Delay, Sensory Disorders. Basic parameters: 4 years — 8 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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.

Detailed description

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

Interventions

  • Behavioral Aquatic Therapy
    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 goal

Primary outcome measures

  • Change in Total Sensory Systems Score (SPM-2) [Time frame: 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. [Time frame: Baseline (pre-intervention) and immediately after completion of the intervention period (post-intervention).]

Eligibility criteria

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.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07646951 · RE/2111/MTI.PT/2605121

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗