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Not yet recruitingNCT07646951AQUA vs SRI TrUpdated Jun 15, 2026

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

An interventional study of Aquatic Therapy in Neuro Developmental Delay and Sensory Disorders, sponsored by MTI University. Not yet recruiting. Open to participants aged 4 Years to 8 Years. Per ClinicalTrials.gov, last updated 2026-06-15.

Sponsored by MTI University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
4 Years to 8 Years
Sex
All
01

Study summary

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.

Read the 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
02

Conditions studied

  • Neuro Developmental Delay
  • Sensory Disorders

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Keywords

  • Aquatic Therapy vs Sensory Room + SPD + Children
  • sensory disorder - aquatic therapy
03

In context

Sensation Disorders

87 studies on the registry are indexed under Sensation Disorders; 23 are open to participants now.

This study's planned enrollment of 60 is above the median of 40 across 56 interventional studies indexed under Sensation Disorders.

Browse Sensation Disorders studies →

Lead sponsor

MTI University is the lead sponsor of 61 studies on the registry; 11 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
4 Years to 8 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Children aged 4-8 years with a confirmed diagnosis of monochannel sensory processing disorder.

Exclusion criteria

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.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    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.

    Behavioral: Aquatic Therapy

Interventions

  • BehavioralAquatic 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 goals.

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What researchers measure

Primary outcomes

  1. Change in Total Sensory Systems Score (SPM-2)

    Time frame: Baseline (pre-intervention) and immediately after completion of the intervention period (post-intervention).

  2. Significant improvement in the Total Sensory Systems Score (SPM-2), indicating a shift from monochannel reliance to effective multi-sensory integration.

    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.

    Time frame: Baseline (pre-intervention) and immediately after completion of the intervention period (post-intervention).

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Study locations

No study locations are listed for this record.

08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Jun 2026; primary completion for Nov 2026, 5 months later.

Of 32 interventional studies with no phase under Sensation Disorders, half reached primary completion within 24 months of starting (the median), counting those still running; a quarter within 5 and three quarters within 45. This study's planned 5 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 9, 2026
First posted
Jun 15, 2026
StartEst.
Jun 15, 2026
Primary completionEst.
Nov 15, 2026
CompletionEst.
Dec 20, 2026
Last update
Jun 15, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 15, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07646951
Lead sponsor
MTI University
Responsible party
Rana Nabil Hussein Mohamed (Lecture of pediatric physical therapy, MTI University) — Principal investigator
First posted
Jun 15, 2026
Start date
Jun 15, 2026 (estimated)
Primary completion
Nov 15, 2026 (estimated)
Completion
Dec 20, 2026 (estimated)
Last update
Jun 15, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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