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NCT07590245Completed

Comparative Effects of Sensorimotor Interventions on Hand Performance With Stroke

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

Source: ClinicalTrials.gov · Last updated 18 May 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
81 (actual)
First submitted
11 May 2026
Start date
6 Mar 2026
Primary completion date
25 Apr 2026
Lead sponsor
Atlas University
Diseases
Stroke
NCT number
NCT07590245

What you commit to

  • Study type: Interventional
  • Participants enrolled: 81
  • From 6 Mar 2026 to the primary completion date, 25 Apr 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • History of surgery on the upper extremity
  • Having a rheumatic disease
  • Having a neurological condition in the upper extremity
  • Having a severe mental or cognitive impairment

Other

  • Having joint movement restriction in the upper extremity
  • Presence of skin injury or scarring on the hand or wrist
  • Having an orthopedic problem in the upper extremity

Who the study is looking for

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

Age in the registry: 45 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Istanbul Atlas University
Coordinator of this site? Confirm its status
KâğıthaneTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.