Comparative Effects of Sensorimotor Interventions on Hand Performance With Stroke
15 maggio 2026 aggiornato da: 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.
Panoramica dello studio
Stato
Completato
Intervento / Trattamento
Tipo di studio
Interventistico
Iscrizione (Effettivo)
81
Fase
- Non applicabile
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Luoghi di studio
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Istanbul
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Kâğıthane, Istanbul, Turchia (Türkiye), 34408
- Istanbul Atlas University
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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
- Adulto
- Adulto più anziano
Accetta volontari sani
No
Descrizione
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
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: Altro
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Separare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
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Sperimentale: Sensory Exercise Group
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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.
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Sperimentale: Motor Exercise Group
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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.
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Sperimentale: Combined Sensory and Motor Exercise Group
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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.
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Nessun intervento: 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.
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
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Moberg Pick-up Test (MPUT)
Lasso di tempo: immediately after the intervention
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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
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immediately after the intervention
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Muscle Reaction Time
Lasso di tempo: immediately after the intervention
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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.
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immediately after the intervention
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Grip Strength (Measured Using Jamar Electronic Dynamometer)
Lasso di tempo: immediately after the intervention
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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.
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immediately after the intervention
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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 (Effettivo)
6 marzo 2026
Completamento primario (Effettivo)
25 aprile 2026
Completamento dello studio (Effettivo)
1 maggio 2026
Date di iscrizione allo studio
Primo inviato
11 maggio 2026
Primo inviato che soddisfa i criteri di controllo qualità
11 maggio 2026
Primo Inserito (Effettivo)
15 maggio 2026
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
18 maggio 2026
Ultimo aggiornamento inviato che soddisfa i criteri QC
15 maggio 2026
Ultimo verificato
1 marzo 2026
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- 2024-ATLAS-MSEHF-005
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
NO
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 .
Prove cliniche su The Sensory Exercise Group
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Children's Hospital Los AngelesAmerican Psychological FoundationReclutamento