Trials / Unknown
UnknownNCT06050590
NeuroGlove PTSD Study
Impact of Peripheral Sensory Stimulation of the Hand and Synchronized Deep Breathing in the Treatment of Post-Traumatic Stress Disorder: Assessing Safety and Effectiveness
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 6 (estimated)
- Sponsor
- NeuroGlove LLC · Industry
- Sex
- All
- Age
- 18 Years – 85 Years
- Healthy volunteers
- Not accepted
Summary
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.
Detailed description
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. There will be a single cohort in the study consisting of the subjects with PTSD who will receive treatment with NeuroGlove. The trial is intended to evaluate the impact of the device use on active PTSD symptoms and subject sense of well-being.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | NeuroGlove | Study participant with PTSD will undergo daily at home treatment using the NeuroGlove. |
Timeline
- Start date
- 2023-08-14
- Primary completion
- 2024-08-27
- Completion
- 2024-09-01
- First posted
- 2023-09-22
- Last updated
- 2024-08-27
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT06050590. Inclusion in this directory is not an endorsement.