NeuroGlove PTSD Study

Status unconfirmed · Not applicable

Conditions studied: PTSD, Post Traumatic Stress Disorder

In brief

This is a prospective, home-based, interventional clinical study in which 6 subjects will be enrolled. Six (6) subjects who suffer from post-traumatic stress disorder will receive treatment using the NeuroGlove.

Key facts

Study ID

NCT06050590

Run by

NeuroGlove LLC

People needed

6

Starts

2023-08-14

Expected to finish

2024-09-01

Last updated by the study team

2024-08-27

Who can join

Age: 18 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Able to and willing to provide informed consent. Legally authorized representatives (LARs) will not be allowed to consent on behalf of the subject.
• Men and women ≥18 and <85 years of age.
• Carry an active diagnosis of PTSD.
• Suffer from PTSD symptoms that impact subject's daily activities and quality of life.

You may not qualify if…

• Physical limitations of the upper extremity (e.g., fracture, joint deformity, severe spasticity/contracture, wounds, skin breakdown, lymphedema, etc.)
• Subject lacks the ability to comprehend or following instructions, or for any reason, in the opinion of the investigator, would be unlikely or unable to comply with study protocol requirements.
• Currently participating in another interventional clinical trial. (Observational clinical trial participation is allowed for study enrollment.)

Where it is running

• NeuroGlove — Saint Paul, Minnesota, United States

Full record on ClinicalTrials.gov

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