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
調査の概要
詳細な説明
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
研究の種類
入学 (推定)
段階
- 適用できない
参加基準
適格基準
就学可能な年齢
- 子
健康ボランティアの受け入れ
説明
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.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的: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.
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Change in Total Sensory Systems Score (SPM-2)
時間枠: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).
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|
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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.
時間枠: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.
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Baseline (pre-intervention) and immediately after completion of the intervention period (post-intervention).
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協力者と研究者
スポンサー
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- RE/2111/MTI.PT/2605121
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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