Using the Gigstride device to help patients with lower extremity deficits
Use Of Gigstride Device In Patients With Lower Extremity Deficit
This study is testing if the Gigstride device can help people with walking difficulties feel more stable and move better after their treatment.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 20 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Johns Hopkins University Academic / other |
| Locations | 1 site (Baltimore, Maryland) |
| Trial ID | NCT06548087 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of the Gigstride ambulatory device in patients with lower extremity mobility deficits. It aims to assess patient satisfaction and the device's impact on biomechanics, walking speed, and stability. The Gigstride device utilizes elastic cords to enhance movement and balance, potentially improving the user's ambulation experience. Participants will be individuals who have previously undergone treatment for conditions affecting their lower extremities.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 who have undergone treatment for lower extremity mobility deficits, such as osteoarthritis or post-surgical rehabilitation.
Not a fit: Patients who are unable to walk or have had shoulder operations within the past year may not benefit from this study.
Why it matters
Potential benefit: If successful, this device could significantly improve mobility and quality of life for patients with lower extremity deficits.
How similar studies have performed: While the Gigstride device represents a novel approach, similar studies on ambulatory aids have shown promising results in improving mobility.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Male or female, age \> 18 * Has undergone treatment for a lower extremity mobility deficit, with one of the following causatives Principal Diagnoses Osteoarthritis hip, knee, spine Pre or post hip replacement Pre or post knee replacement Multiple Sclerosis Mild to moderate central spinal stenosis Foot drop Degenerative changes, not otherwise specified Balance issues * Recommended cane, brace, walker, Ankle Foot Orthoses, or electronic or robotic device for management * Provide written consent for participation. * Ability to wear shoes with laces Exclusion Criteria: * Inability to walk. * Shoulder operation within 1 year preceding the study date. * Injury due to a work accident (e.g. workers comp) * Higher functions do not enable proper comprehension of protocol or reliable data recording.
Where this trial is running
Baltimore, Maryland
- Johns Hopkins University — Baltimore, Maryland, United States (Recruiting)
Study contacts
- Principal investigator: Akhil Chhatre, MD — Johns Hopkins University
- Study coordinator: Akhil Chhatre, MD
- Email: chhatre@jhu.edu
- Phone: (443) 561-4201
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.