Effect of a special splint on finger motion recovery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

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.

Why it matters

Who can join: the full rules

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 it's running

• 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

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.