Upper Extremity Dysfunction

7

Review clinical trials related to Upper Extremity Dysfunction. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Nerve Transfer Surgery to Restore Upper-limb Function After Cervical Spinal Cord Injury

The goal of this prospective, open-label cohort study is to assess functional outcomes in individuals with cervical spinal cord injury who have undergone nerve transfer surgery to restore upper limb function. The main questions it aims to answer are: * Does nerve transfer improve hand function in individuals with cervical spinal cord injury? * What factors are associated with functional improvement following nerve transfer? Researchers will compare functional outcomes at 24 months post-surgery to 1) baseline outcomes and 2) individuals with cervical spinal cord injury who did not undergo nerve transfer. Participants who have received nerve transfer surgery as part of their regular medical care will complete functional hand tests, electrodiagnostic assessments, and questionnaires on independence and mood every 3 months for 24 months after surgery.

Participants needed: 40
Trial details
Age: 18-70Biological sex: AllType: ObservationalSponsor: University of British ColumbiaUpdated: May 29, 2026Locations: 4Duration: 2 Years
Eligibility criteria

Traumatic, motor-complete cervical SCI (AIS A or B) [+8]

Inability or unwillingness to participate in post-operative rehabilitation (in p... [+1]

Status: Recruiting

Comparison of the Effects of Mirror Therapy,rTMS and Robotic-assisted Hand Therapy in Stroke Patients

The aim of the study is to investigate the comparison of the effects of mirror therapy, Repetitive Transcranial Magnetic Stimulation and robot-assisted hand therapy added to conventional neurological rehabilitation on upper extremity function, quality of life and pain in stroke.

Participants needed: 120
Trial details
Age: 40-80Biological sex: AllType: InterventionalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Mar 12, 2026Locations: 1
Eligibility criteria

Patients who applied to Afyonkarahisar Health Sciences University Hospital Physi...

Female and male patients between the ages of 40-80 [+23]

Status: Recruiting

Wearable Focal Vibration Therapy on Upper Extremity Function of People With Multiple Sclerosis: A Pilot Study

This pilot mixed-method study will evaluate the feasibility, preliminary efficacy, and user experience of a home-based wearable Focal Vibration Therapy (FVT) intervention for improving upper extremity (UEx) function in people with multiple sclerosis (MS). Fifteen adults with relapsing-remitting MS (PRMS) and self-reported UEx impairments will participate in a 4-week FVT program using MyovoltTM wearable FVT devices applied to arm muscles.

Participants needed: 15
Trial details
Age: 18-100Biological sex: AllType: InterventionalSponsor: University of FloridaUpdated: Mar 6, 2026Locations: 2
Eligibility criteria

Aged over 18 years [+8]

Evidence of cognitive impairment that could interfere with following instruction... [+3]

Status: Recruiting

Mirror vs Virtual Reality Therapy for Upper Extremity Function in Hemiplegic Patients

Upper extremity impairment in hemiplegic patients significantly impacts daily activities and reduces quality of life. Although traditional rehabilitation methods can help, some patients experience limited progress. Recently, modern techniques such as mirror therapy and virtual reality (VR) have emerged, demonstrating promising results in motor skill improvement. This study aims to directly compare the acute effects of mirror therapy and VR therapy on upper limb motor function in hemiplegic patients. Forty-two participants aged 18-75 with hemiplegia due to stroke (6-12 months post-stroke) will be randomly assigned to either mirror therapy or VR therapy. The evaluation includes motor function (Fugl-Meyer Assessment), spasticity (Modified Ashworth Scale), activities of daily living (Barthel Index), fine motor skills (Box and Block Test), proprioception, and reaction time. The goal is to identify the effectiveness of the mirror therapy and VR therapy on motor function, spasticity control, proprioception, daily activity performance, and reaction times, contributing valuable insights to clinical rehabilitation practices.

Participants needed: 42
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Istinye UniversityUpdated: Mar 2, 2026Locations: 1
Eligibility criteria

Hemiplegic patients in need of upper extremity rehabilitation. [+5]

Patients with severe spasticity (score ≥ 3 on the Modified Ashworth Scale) [+3]

Status: Recruiting

Effects of Combined vs. Sequential Attentional Focus Instructions on Upper Extremity Function in Subacute Stroke

Stroke is a leading cause of long-term disability, and upper extremity impairments-affecting about 80% of survivors-limit functional reach, grasp, and manipulation more severely than lower limb deficits. Despite partial recovery of walking ability, meaningful functional use of the paretic arm remains limited. Conventional rehabilitation often lacks sufficient intensity, task specificity, and motor learning principles, highlighting the need for more effective approaches. The subacute phase of stroke (up to 6 months post-onset) represents a period of heightened neuroplasticity and strong rehabilitation potential. During this time, integrating cognitive and motor training-such as attentional focus strategies-has gained attention. External focus enhances movement efficiency through motor automaticity, whereas internal focus supports early motor control. Evidence suggests that combining these strategies may optimize recovery, yet their relative effectiveness in stroke rehabilitation remains unclear. Two main instructional approaches exist: combined attentional focus (internal and external cues delivered within the same session) and sequential attentional focus (internal focus first, followed by external focus as control improves). While both show therapeutic promise, comparative data in stroke populations are lacking. This study aims to compare combined versus sequential attentional focus instructions in improving upper extremity function in subacute stroke. We hypothesize that a combined approach-starting with internal focus early, then integrating external focus-will yield superior motor improvements.

Participants needed: 36
Trial details
Age: 40-80Biological sex: AllType: InterventionalSponsor: Bahçeşehir UniversityUpdated: Jan 20, 2026Locations: 1
Eligibility criteria

Age 40-80 years at enrollment (Kwakkel et al., 1996; Coupar et al., 2012). [+7]

Spasticity level: Individuals with a Modified Ashworth Scale (MAS) score ≥3 in e... [+5]

Status: Recruiting

The Utilization Effects of Powered Wearable Orthotics in Improving Upper Extremity Function and ADL in Persons With SCI

To evaluate the usefulness of an upper extremity assistive device, called (MyoPro) in improving upper extremity activities in people with incomplete spinal cord injury. The Department of Defense is supporting this study.

Participants needed: 60
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Kessler FoundationUpdated: Nov 24, 2025Locations: 1
Eligibility criteria

Be between ages 18-80 [+10]

Be younger than 18 years old or older than 80 [+9]

Status: Not yet recruiting

Trunk and Upper Extremities Program Effect in Decreasing Compensation Patterns in Unilateral Cerebral Palsy Children

The goal of this clinical trial is to test the effectiveness of a trunk and upper extremities exercise program. The main questions it aims to answer are: Whether the program decreases compensation patterns in unilateral cerebral palsy children Whether the program decreases pain in unilateral cerebral palsy children Whether the program improves bimanual ability in unilateral cerebral palsy children Participants will undertake and 8-week program exercise at home If there is a comparison group: Researchers will compare with the control group to see if this program decreases compensation patterns.

Participants needed: 40
Trial details
Age: 8-16Biological sex: AllType: InterventionalSponsor: Fundacio Aspace CatalunyaUpdated: Feb 14, 2025
Eligibility criteria

Unilateral cerebral palsy diagnostic [+1]

Have received any intervention with botulinum toxin or shock waves in the previo... [+5]