Effect of a special splint on finger motion recovery
Pilot Study on The Effectiveness of Relative Motion Orthosis in Finger Motion
This study is testing if a special splint can help people aged 18 to 80 with stiff fingers from injuries move their fingers better compared to just regular care.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 64 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | NYU Langone Health Academic / other |
| Locations | 1 site (New York, New York) |
| Trial ID | NCT06646029 on ClinicalTrials.gov |
What this trial studies
This pilot study aims to assess the effectiveness of a Relative Motion Orthosis (RMO) in improving finger range of motion in patients with stiffness in the Proximal Interphalangeal (PIP) joint due to injury. Participants will be randomly assigned to receive either standard care or standard care plus the RMO. The primary goal is to evaluate the improvement in finger motion using clinical assessments and physical examinations. The study focuses on individuals aged 18 to 80 with specific PIP injuries that limit their finger extension.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 18-80 with PIP injuries causing reduced active range of motion in extension.
Not a fit: Patients with severe arthropathy or those requiring serial casting for their PIP joint stiffness may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance recovery of finger motion for patients suffering from PIP joint stiffness.
How similar studies have performed: While this approach is novel, similar studies have shown promise in improving joint motion with specialized orthotic devices.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age range 18-80 * Any gender * Any Proximal Interphalangeal (PIP) injury that causes reduced PIP Active Range of Motion (AROM) in extension * Right or left hand injury * Level of Chronicity (4 weeks - 6 months) * Able to follow instructions Exclusion Criteria: * PIP with hard end feel (feels they need serial casting) - level of chronicity * Any digital nerve injury / skin laceration that can prevent the patient from using the orthosis * Severe arthropathy * Literacy deficits: patients need to be able to follow verbal and written instructions independently to minimize risks and improve outcomes from care.
Where this trial is running
New York, New York
- NYU Langone Health — New York, New York, United States (Recruiting)
Study contacts
- Principal investigator: Natalia Ruiz, DPT — NYU Langone Health
- Study coordinator: Natalia Ruiz, DPT
- Email: Natalia.ruiz@nyulangone.org
- Phone: 646-501-4782
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.