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NCT03412656 · ClinicalTrials.gov registry record · NA

Assessing Force Feedback With the SoftHand Pro

A NA study of Amputation, Traumatic and Limb Defect, sponsored by Kristin Zhao, PhD.

Completed
Registry status
NA
Development phase
27
Enrollment target
1
Study location

NCT03412656 is a NA study of Amputation, Traumatic and Limb Defect that has completed, run by Kristin Zhao, PhD. The registered enrollment target is 27 participants, below the 51-participant average among 11 other Amputation, Traumatic trials with a reported enrollment target (47% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03412656, a NA study of Amputation, Traumatic and Limb Defect, has completed, sponsored by Kristin Zhao, PhD.

COMPLETED
Registry status
NA
Development phase
27 participants
Enrollment target
1
Study location

Study Summary

The trial is designed to test the effectiveness of a force-feedback cuff in combination with a myoelectric prosthesis in conveying information on grasp strength to the user, as well as the user's preference regarding the feature.

Interventions

  • DEVICE SoftHand Pro with CUFF force feedback device

Study Locations (1)

Minnesota

  • Mayo Clinic in Rochester - Rochester

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2017-10-17
Est. Completion 2019-06-14
Phase NA

Sponsor

Kristin Zhao, PhD

5 total trials

What the Registry Record Tells You About NCT03412656

The ClinicalTrials.gov registry entry for NCT03412656 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 27 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 51-participant average among 11 other Amputation, Traumatic trials with a reported enrollment target (47% lower). The listed sponsor is Kristin Zhao, PhD, which has 5 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Amputation, Traumatic appearing as the primary indexed condition, and to 1 intervention - of which SoftHand Pro with CUFF force feedback device is the first listed.

NCT03412656 reports 1 study location spanning 1 distinct geographic area - top geographies include Minnesota.

Frequently Asked Questions

What is clinical trial NCT03412656 about?

NCT03412656 is a clinical study titled "Assessing Force Feedback With the SoftHand Pro". The trial is designed to test the effectiveness of a force-feedback cuff in combination with a myoelectric prosthesis in conveying information on grasp strength to the user, as well as the user's preference regarding the feature.

What is the current status of trial NCT03412656?

This trial is currently completed. It is a NA study. The enrollment target is 27 participants. The study started on 2017-10-17. Estimated completion is 2019-06-14.

What conditions does trial NCT03412656 study?

This clinical trial studies the following conditions: Amputation, Traumatic, Limb Defect.

What interventions are being tested in trial NCT03412656?

The interventions under investigation include: SoftHand Pro with CUFF force feedback device (DEVICE).

Who is sponsoring clinical trial NCT03412656?

This trial is sponsored by Kristin Zhao, PhD, which has 5 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03412656 being conducted?

This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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