Overview
The goal of this clinical trial is to evaluate the applicability, effectiveness, and usability of a shape memory alloy-based orthosis for patients with finger proximal interphalangeal joint stiffness. This cutting-edge design incorporates shape memory alloy into the device for improving proximal interphalangeal joint stiffness and, secondarily, enhancing the ability to perform activities.
Half of the participants will be assigned to experimental group, receiving a shape memory alloy-based orthosis for home program. The other half will be assigned to control group, receiving a conventional stretching program. Three evaluations, examining range of motion and hand functional performance, will be conducted before intervention, 4 weeks and 8 weeks after baseline by the researchers.
Eligibility
Inclusion Criteria:
- 18-79 years old
- Exhibit limitations in passive range of motion of the proximal interphalangeal joint, with extension less than 0 degrees or flexion less than 90 degrees.
- Beyond the acute phase of the hand condition, and it has been more than 8 weeks post-surgery (or post-injury).
Exclusion Criteria:
- Concurrently use other types of splints for PIP joint stiffness.
- Present with abnormal muscle tone, paralysis, or rigidity associated with central or peripheral nervous system dysfunction.
- Suffer from complex regional pain syndrome or progressive degenerative disease affecting finger joints, such as rheumatoid arthritis.
- Have an active infection or arthritis in their fingers.
- Unable to follow instructions.