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Investigating the efficacy of two exercise protocols following fracture and open surgical fixation of the proximal phalangeal bone in the finger.

Not Applicable
Completed
Conditions
Open reduction and internal fixation (ORIF) following finger proximal phalanx fracture.
Injuries and Accidents - Fractures
Registration Number
ACTRN12610000294055
Lead Sponsor
A/Prof Jack Crosbie
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
66
Inclusion Criteria

All adults (age range: 18- 65 years of age) with finger proximal phalangeal fractures that were stabilised via open reduction internal fixation (with plate and screw fixation or screw fixation alone) at Sydney Hospital Hand Unit are candidates for inclusion in the study. Participants must also have a willingness to give written informed consent and willingness to participate in and comply with the study.

Exclusion Criteria

(1) there was a delay between fracture and surgical fixation greater than two weeks,
(2) the surgical procedure did not achieve stability,
(3) there is the presence of co- morbidities including diabetes and active arthropathy,
(4) there is concomitant tendon or nerve injury, other fracture or vascular injury,
(5) there are cognition problems or poor pain awareness,
(6) there is an inability to attend regular hand therapy follow- up appointments.
(7) patients with a history of a psychological illness or condition such as to interfere with the patient's ability to understand the requirements of the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Total active range of motion of the injured finger measured using a finger goniometer.[Enrolment visit; 6 weeks; and 12 weeks];Grip strength measured using the hand held Jamar Dynamometer.[6 weeks; and 12 weeks after surgery];Active extension at the proximal interphalangeal (PIP) joint of the injured finger measured using a finger goniometer.[Enrolment visit; 6 weeks; and 12 weeks after surgery]
Secondary Outcome Measures
NameTimeMethod
Activity limitation and participation levels will be measured via the Patient Rated Wrist and Hand Evaluation (PRWHE) questionnaire.[12 weeks after surgery]
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