Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT05417828 · ClinicalTrials.gov registry record
Robotic Rehabilitation for Stroke Survivors
A clinical trial, sponsored by State University of New York at Buffalo.
- Not yet
- Registry status
- 40
- Enrollment target
NCT05417828: Clinical Trial study, sponsored by State University of New York at Buffalo.
NCT05417828 is a clinical trial that has not yet begun recruiting, run by State University of New York at Buffalo. The registered enrollment target is 40 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05417828 has not yet begun recruiting, sponsored by State University of New York at Buffalo.
- NOT YET RECRUITING
- Registry status
- 40 participants
- Enrollment target
Study Summary
Pilot study on the physiological response of robotic rehabilitation therapy for improving the performance of activities of daily living of stroke patients
Primary Outcome
The max and range of motion of shoulder, elbow, and wrist joint for each task
Interventions
- DEVICE Emulation of Active Daily Living tasks with a robotic device (SPINDLE)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2025-12-01 |
| Est. Completion | 2026-12-05 |
What is known before NCT05417828 opens enrollment
NCT05417828 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 40 participants, a relatively small participant target.
The record links to 0 conditions, and to 1 intervention - of which Emulation of Active Daily Living tasks with a robotic device (SPINDLE) is the first listed.
NCT05417828 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT05417828 about?
NCT05417828 is a clinical study titled "Robotic Rehabilitation for Stroke Survivors". Pilot study on the physiological response of robotic rehabilitation therapy for improving the performance of activities of daily living of stroke patients
What is the current status of trial NCT05417828?
This trial is currently not yet recruiting. The enrollment target is 40 participants. The study started on 2025-12-01. Estimated completion is 2026-12-05.
What interventions are being tested in trial NCT05417828?
The interventions under investigation include: Emulation of Active Daily Living tasks with a robotic device (SPINDLE) (DEVICE).
Who is sponsoring clinical trial NCT05417828?
This trial is sponsored by State University of New York at Buffalo, which has 243 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT01306019 · 40 participants · Phase 1
Lentiviral Gene Transfer for Treatment of Children Older Than Two Years of Age With X-Linked Severe Combined Immunodeficiency (XSCID)
- NCT01608152 · 40 participants
Development of a Video Game for the Improvement of Outcomes in Stem Cell Transplant Survivors
- NCT01668082 · 40 participants · NA
An Investigation of Brain Tumor Metabolism in Patients Undergoing Surgical Resection
- NCT02015013 · 40 participants · Phase 2
Hematopoietic Stem Cell Mobilization in Idiopathic CD4 Lymphocytopenia Patients and Healthy Controls for the Study of T Cell Maturation and Trafficking in Murine Models
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI