Upper Extremity Problem

3

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

Condition / disease
Location
Status: Recruiting

Vivistim Registry for Paired VNS Therapy (GRASP)

The purpose of the Vivistim Registry for Paired VNS Therapy (GRASP) is to gather real-world information on patients with arm and hand deficits post-stroke who are considering Vivistim System treatment. Before and after Vivistim System implant, patient data will be collected and reported throughout the therapy process. Physicians or sites will receive appropriate remuneration for the effort and cost involved in collecting and transmitting this data to MicroTransponder Inc.

Participants needed: 1,000
Trial details
Age: 22+Biological sex: AllType: ObservationalSponsor: MicroTransponder Inc.Updated: Jun 29, 2026Locations: 15Duration: 3 Years
Eligibility criteria

Patients implanted with the Vivistim System for upper limb deficits associated w...

Not eligible for surgery

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: Recruiting

Effects of Biofeedback-Guided Training on Muscle Strength and Postural Alignment in Upper Cross Syndrome.

This randomized controlled trial investigates the effects of biofeedback-guided training versus conventional therapy on muscle strength and postural alignment in patients with Upper Cross Syndrome. The study includes adults aged 25-45 years meeting diagnostic criteria for UCS, such as weak deep cervical flexors, restricted cervical ROM, forward head posture, increased thoracic kyphosis, and chronic neck pain \>3 months. Participants are divided into two groups: Group A biofeedback training and Group B conventional therapy, receiving 12 sessions over 4 weeks ,3sessions/week. Assessments are conducted at baseline, post-1st session, and weekly intervals using standardized measures.The study aims to compare the efficacy of biofeedback-guided training in improving strength and posture in UCS patients.

Participants needed: 56
Trial details
Age: 25-45Biological sex: AllType: InterventionalSponsor: Riphah International UniversityUpdated: Aug 22, 2025Locations: 1
Eligibility criteria

• Adults aged 25-45 years with both genders. [+4]

• History of recent neck surgery or injury. [+3]