Physiotherapy vs Telerehabilitation After Volar Plating of Distal Radius Fracture

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorTöölö Hospital

About this trial

Trial purpose is to research the outcome comparing traditional physiotherapy vs telerehabilitation after volar plating of distal radius fracture.

Patients with distal radius fracture that meet the operative criteria set by the Finnish Current Care guidelines are randomized (1:1 computer generated sequence with random block size) to two parallel groups and will undergo operative treatment and traditional physiotherapy vs telerehabilitation.

Baseline data is collected preoperatively and patients are followed at 1, 3 and 12 months after enrollment. The primary end-point is 3 months and the primary outcome is the Patient-Rated Wrist Evaluation (PRWE).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Distal radius fracture, which applies the surgical requirements

age between 18 to 65 years

Non concomitant injuries including ligament injuries and distal ulna fractures, however ulnar styloid avulsion is accepted

No significant comorbidities

Disqualifiers

High energy or multiple injuries

Open fractures

Injury of both upper extremities

Other operative injury on the same side

Trial design

Design model

Parallel

Treatments tested in this trial

  • Telerehabilitation

    Other intervention

    Telerehabilitation program

  • Traditional physiotherapy

    Other intervention

    Guided rehabilitation program with physiotherapist appointments

Treatment groups

84 Participants
are divided into 2 treatment groups
Group A: TelerehabilitationExperimental treatment 1 intervention
Group B: Traditional PhysiotherapyActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Patient-Rated Wrist Evaluation (PRWE)

The PRWE comprises 15 questions to measure wrist pain and disability in daily activities. In PRWE patients rate wrist pain and disability from 0 to 10 and it consists two subscales: Pain and Function (0=best possible outcome, 10=worst possible outcome)

Time frame
12 months

Secondary outcomes

1

Grip strength

Grip strength is measured with a dynamometer in kg as the mean of three measurements. It will be numbered in kg and percentage of the unaffected side

Time frame
12 months
2

Quick Disabilities of the arm, shoulder, and hand

The QuickDASH is self-reported questionnaire and shortened version of DASH outcome measure to measure physical function and symptoms in people with any or multiple musculoskeletal disorders of the upper limb in 11 dimensions in 1-5 scale (1=best possible outcome, 5=worst possible outcome)

Time frame
12 months
3

Pain (Visual Analogue Scale)

The VAS is derived by health care professional question of pain in scale 0 to 10 (0=no pain, 10=worst possible pain).

Time frame
12 months
4

Wrist range of motion (ROM)

Wrist ROM is measured on both wrists with a handheld goniometer in degrees.

Time frame
12 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Töölö Hospital

Lead sponsor

Hospital District of Helsinki and Uusimaa

Sponsor institution