Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06985459

Effectiveness of Exercise Relative Motion Orthoses for Limited Finger Joint Motion

Led by Insel Gruppe AG, University Hospital Bern · Updated on 2025-05-29

148

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This randomized controlled trial investigates the effectiveness of two exercise orthosis designs-the Relative Motion Flexion (RMF) and Relative Motion Extension (RME) orthoses-for improving motion in patients with proximal interphalangeal joint (PIPJ) flexion or extension deficits. A total of 148 adult patients with acute hand injuries and a minimum 10° difference between active and passive PIP joint motion will be enrolled. Participants are stratified by their primary motion deficit and randomized to either the exercise orthosis or placebo orthosis group. The orthosis is worn for 4 weeks, with follow-up assessments at weeks 6 and 8 to evaluate range of motion and patient satisfaction. All participants will continue standard hand therapy throughout the study.

CONDITIONS

Official Title

Effectiveness of Exercise Relative Motion Orthoses for Limited Finger Joint Motion

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • PIPJ motion deficit with at least a 10° difference between passive and active motion
  • Acute injury operated on or within 6 weeks of the accident
  • Only one hand affected
  • Adult patients over 18 years old
  • Ability to understand German, French, or English
  • Receiving hand therapy treatment at Inselspital in Bern
  • Able to provide informed consent by signing
Not Eligible

You will not qualify if you...

  • Previous hand or PIPJ injuries limiting joint mobility, such as fractures or ligament damage
  • Having osteoarthritis or rheumatoid arthritis affecting finger joint stiffness, pain, or inflammation
  • Unable to follow study procedures due to language issues, psychological disorders, or dementia
  • Having boutonniere deformity
  • Being under 18 years old

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Hospital Bern

Bern, Canton of Bern, Switzerland, 3010

Actively Recruiting

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Research Team

B

Bernadette Tobler-Ammann, PhD

CONTACT

E

Esther Vögelin, Prof, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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