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Comparative Effects of Sensorimotor Interventions on Hand Performance With Stroke

2026年5月15日 更新者:Gamze Demircioğlu、Atlas University

Comparative Effects of Sensorimotor Interventions on Hand Motor Function and Performance in Patients With Stroke

This randomized controlled trial investigated the comparative effects of sensory, motor, and combined sensorimotor interventions on hand motor function and behavioral performance in patients with stroke. The study focused on upper-extremity impairments, particularly deficits in hand strength, dexterity, and reaction time, which are common following stroke and substantially limit functional independence. Sensorimotor integration plays a critical role in motor recovery, as effective hand function depends on the interaction between sensory feedback and motor control mechanisms.

Participants with stroke were randomly assigned to sensory, motor, or combined sensorimotor intervention groups. The interventions were designed to target tactile perception, motor coordination, and integrated sensorimotor processing through attended active and passive stimulation approaches. Outcome measures included hand grip strength, manual dexterity, and reaction time, which were evaluated before and after the intervention period.

The findings demonstrated that sensorimotor-based rehabilitation approaches positively influenced upper-extremity motor performance and behavioral responses in stroke patients. In particular, combined sensorimotor interventions appeared to provide more comprehensive improvements by simultaneously enhancing sensory processing and motor execution. These results support the importance of integrating sensory-focused strategies into conventional motor rehabilitation programs to optimize neuroplasticity and functional recovery after stroke. The study contributes to the growing evidence supporting multidimensional rehabilitation approaches for improving hand function and sensorimotor performance in individuals with stroke.

調査の概要

研究の種類

介入

入学 (実際)

81

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • Istanbul
      • Kâğıthane、Istanbul、トルコ(Türkiye)、34408
        • Istanbul Atlas University

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  • Having the ability to verbally communicate to answer questions
  • Willingness to participate in the study
  • Having read and signed the informed consent form

Exclusion Criteria:

  • Having joint movement restriction in the upper extremity
  • Presence of skin injury or scarring on the hand or wrist
  • History of surgery on the upper extremity
  • Having an orthopedic problem in the upper extremity
  • Having a rheumatic disease
  • Having a neurological condition in the upper extremity
  • Having a severe mental or cognitive impairment

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

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:他の
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:独身

武器と介入

参加者グループ / アーム
介入・治療
実験的:Sensory Exercise Group
The Sensory Exercise Group (SEG) participated in an intervention designed to enhance sensory awareness and integration. The protocol included tactile stimuli such as sand, sensory balls, fabrics with different textures, multisensory gels, brushing, vibration, and superficial massage to stimulate cutaneous receptors and enrich sensory input. Massage was applied with the participant in a supine position, elbows extended, and hands in a neutral position. All sessions were standardized using a digital stopwatch, and each intervention lasted approximately 15 minutes with equal time allocation across groups. This standardized timing ensured that observed effects were related to the intervention content rather than differences in exposure duration.
実験的:Motor Exercise Group
The Motor Exercise Group (MEG) performed structured hand exercises including active range of motion exercises for the wrist and fingers, grip strengthening, stabilization exercises, and wrist flexion-extension exercises using elastic bands and dumbbells. Resistance levels were adjusted according to participant tolerance, and the protocol was applied only to the dominant side. Each exercise consisted of 5-7 repetitions and two sets, with 30-second rest intervals between sets.
実験的:Combined Sensory and Motor Exercise Group
In the Combined Sensorimotor Group (CSMG), sensory and motor exercises were applied according to the protocols used in the Sensory Exercise Group (SEG) and Motor Exercise Group (MEG). However, each exercise was performed as a single set, with the remaining session time allocated to superficial massage and sensory stimulation. The sensory and motor components were administered sequentially, with each phase lasting approximately 7-8 minutes to maintain temporal balance within the session.
介入なし:Control
The control group did not receive any additional treatments during the study period, allowing for a clear comparison between the experimental group and the baseline conditions.

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
Moberg Pick-up Test (MPUT)
時間枠:immediately after the intervention
Hand function was evaluated using the Moberg Pick-up Test (MPUT), a standardized method for assessing functional hand use and fine-motor skills, specifically measuring the ability to grasp and manipulate small objects. During the test, participants were instructed to pick up various small objects (e.g., coins and small blocks) and place them in a container as quickly as possible. During the test, the participants were instructed to pick up various small objects and place them in a container as quickly as possible. The assessment was conducted with the dominant hand, first with eyes open and then with eyes closed, to test sensory function. For each condition, the test was repeated three times, and the best performance time, recorded in seconds, was used for analysis. The objects used in the test were of similar size and required coordinated hand movements for successful completion, ensuring consistency in task difficulty
immediately after the intervention
Muscle Reaction Time
時間枠:immediately after the intervention
Light Trainer® system, which consists of a wireless lighting system with LED pods and a central controller. The participants were seated with their hands on the table, 40 cm apart, palms down, and elbows at 90°. The Light Trainer was positioned centrally 20 cm away from each hand. When the pod was illuminated, the participants were instructed to turn off the light as quickly as possible by touching it. Light activation was randomized to avoid predictability, requiring participants to respond based on light cues each time. In the first task, the participants used their dominant hand to turn off the light as quickly as possible. In the second task, they responded to a light signal by deactivating a predetermined light from two different colors using their dominant hand. Scale Range: No minimum or maximum value in milliseconds (lower time is better). Interpretation: Lower reaction times signify better outcomes, as they reflect faster muscle response to visual stimuli.
immediately after the intervention
Grip Strength (Measured Using Jamar Electronic Dynamometer)
時間枠:immediately after the intervention
Hand performance was assessed based on grip strength using a Takei Handheld Dynamometer (Takei Scientific Instruments Co., Tokyo, Japan). Participants were seated with elbows flexed at 90 degrees and forearms in a neutral position, and were instructed to squeeze the dynamometer with maximum force for 3-5 seconds, with the palm facing upwards. Each hand was tested three times with a 20-second rest between trials, and the highest value was recorded. This protocol ensures standardized and consistent results, with measurements documented in kilograms (kg) to provide reliable grip strength assessment. Scale Range: The dynamometer measures from 0 to 90 kg. Interpretation: Higher scores reflect stronger grip strength, which is indicative of better hand function.
immediately after the intervention

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研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2026年3月6日

一次修了 (実際)

2026年4月25日

研究の完了 (実際)

2026年5月1日

試験登録日

最初に提出

2026年5月11日

QC基準を満たした最初の提出物

2026年5月11日

最初の投稿 (実際)

2026年5月15日

学習記録の更新

投稿された最後の更新 (実際)

2026年5月18日

QC基準を満たした最後の更新が送信されました

2026年5月15日

最終確認日

2026年3月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • 2024-ATLAS-MSEHF-005

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いいえ

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