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Early Active Controlled Motion (EACM) Rehabilitation Protocol Post Open Reduction and Internal Fixation (ORIF) of Scaphoid Fractures: A Pilot Study

Early Active Controlled Motion (EACM) Rehabilitation Protocol Post Open Reduction and Internal Fixation (ORIF) of Scaphoid Fractures: A Pilot Study

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03996512
Enrollment
0
Registered
2019-06-24
Start date
2019-08-01
Completion date
2021-01-19
Last updated
2021-06-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Scaphoid Fixation

Brief summary

There is poor research supporting the benefits of Early Active Controlled Motion (EACM) protocols post operative scaphoid fixation. Advances in surgical fixation technique for scaphoid fractures should allow for start of earlier mobilization, however there is little evidence in the literature that supports the use of these protocols within the early phases of healing. The study uses a pre-experimental design with purposeful sample population recruitment.

Interventions

OTHEREarly Active Controlled Motion (EACM)

Early active controlled wrist motion rehab protocol using that will allow midcarpal row motion.

Sponsors

Performance Health
CollaboratorINDUSTRY
University of Florida
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Date of injury and diagnosis: scaphoid fracture less than 3 weeks old * Waist fractures in the middle 1/3 and distal pole 1/3 of scaphoid bone. * Surgical procedure includes ORIF with screw fixation and/or percutaneous pin with screw fixation. * To be included in the study the patient needs to have started rehab within the first 10 days after surgery date.

Exclusion criteria

* Proximal pole scaphoid fracture * Past medical history of diabetes and other peripheral vascular disorders. * History of osteopenia and osteoporosis. * Previously failed ORIF of scaphoid * Neurovascular or nerve lesion to the involved upper extremity * Cognitive deficits related to memory, attention span, judgment as documented in the EMR or need for a legal guardian to be a medical proxy

Design outcomes

Primary

MeasureTime frameDescription
functional outcome range of motionat entry and up to 12 monthsUsing a goniometer measuring the angle of wrist flexion and extension NEED TO ENTER EXPECTED ROM ranges

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026