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Static vs. Dynamic Progressive Splinting for Persistent Wrist Stiffness After DRF

A

Al Hayah University In Cairo

Status

Enrolling

Conditions

Distal Radius Fractures

Treatments

Behavioral: Static Progressive Splinting for Persistent Wrist Stiffness
Behavioral: Dynamic Splinting for Persistent Wrist Stiffness

Study type

Interventional

Funder types

Other

Identifiers

NCT06913933
SPDS2025-03

Details and patient eligibility

About

This randomized controlled trial will compare the effectiveness of static progressive splinting versus dynamic splinting for treating persistent wrist stiffness in adults ≥18 years old at least 8 weeks post distal radius fracture (DRF) injury. Both splinting modalities are provided as an adjunct to one weekly supervised therapy session over a 6-week period. The primary outcomes are wrist active and passive range of motion (AROM/PROM) measured using goniometry, with secondary outcomes including patient-reported wrist function (PRWE), overall satisfaction, and adverse events.

Enrollment

50 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Adults aged 18 years or older. At least 8 weeks post distal radius fracture (operative or nonoperative) who have completed standard rehabilitation.

Demonstrated persistent wrist stiffness with ≤50% of contralateral wrist extension or flexion.

Capable of providing written informed consent and complying with study procedures

Exclusion criteria

Presence of complex regional pain syndrome (CRPS) or active fracture healing issues.

History of significant wrist pathology unrelated to the DRF. Uncontrolled medical conditions that would interfere with splint application or therapy.

Known skin conditions or allergies that preclude orthosis use. Inability or unwillingness to adhere to the intervention protocol or follow-up schedule.

Pregnant or breastfeeding individuals.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

50 participants in 2 patient groups

Static Progressive Splinting Group (SPSG)
Experimental group
Description:
Participants in this group receive static progressive splinting using a commercial splint that allows incremental adjustment through a turnbuckle design. This splint is used to gradually increase wrist extension and/or flexion, tailored to the patient's stiffness pattern, alongside a once-weekly supervised therapy session.
Treatment:
Behavioral: Static Progressive Splinting for Persistent Wrist Stiffness
Dynamic Splinting Group (DSG)
Experimental group
Description:
Participants in this group receive dynamic splinting using a commercial device equipped with elastic tension (spring-loaded) that provides a constant dynamic stretch to the wrist. This intervention is delivered alongside a weekly supervised therapy session.
Treatment:
Behavioral: Dynamic Splinting for Persistent Wrist Stiffness

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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