Volar Plate Injury: A Comparison of Two Splinting Methods
A Randomised Controlled Trial Investigating the Effectiveness of Two Splinting Methods in the Non-operative Management of Volar Plate Injuries at the Proximal Interphalangeal Joint
1 other identifier
interventional
42
1 country
1
Brief Summary
Which splinting method produces the best outcomes (in range of movement, pain and function) in the non-operative treatment of stable volar plate injuries in adults? The volar plate is a ligament located at the middle knuckle (proximal interphalangeal joint - PIPJ) of the finger. It is commonly injured through hyperextension, for example a ball hitting the fingertip. Current treatment in the Hand Therapy Unit involves splinting the injured joint dorsally (on the back of the finger) into 20⁰ flexion (bent) using thermoplastic material. However, there is a potential risk of developing permanent stiffness of the PIPJ into straightening, once the volar plate ligament heals. To reduce this risk, the study aims to investigate if using a volar (on the front of the finger) gutter splint in 0⁰ flexion (straight), which still prevents hyperextension, achieves better outcomes. There is no existing high-quality evidence comparing these two methods. This is a randomised controlled trial. For the purposes of this study, the current treatment of a 20° dorsal block splint will act as the control group. The intervention group will be the volar gutter splint group. A convenience sample will be used and all patients (over 16 years old) presenting to the Mid Yorkshire Hospitals NHS Trust's Hand Therapy Unit will be invited to participate in the study, with consideration to inclusion/exclusion criteria. Participants will be randomised into one of two groups through the use of a random number generator. The outcomes assessed will be range of movement, pain and function. These will be measured at initial assessment, four and twelve weeks. These are all average normal time intervals that patients are seen. Each splint is worn for four weeks and participants will receive standardised advice, exercises and treatment.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jul 2015
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2015
CompletedFirst Submitted
Initial submission to the registry
August 21, 2015
CompletedFirst Posted
Study publicly available on registry
August 31, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2017
CompletedMarch 21, 2019
March 1, 2019
1.5 years
August 21, 2015
March 19, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Range of movement measured with a Jamar finger goniometer.
Range of movement measured with a Jamar finger goniometer.
One week
Range of movement measured with a Jamar finger goniometer.
Range of movement measured with a Jamar finger goniometer.
Four weeks
Range of movement measured with a Jamar finger goniometer.
Range of movement measured with a Jamar finger goniometer.
Twelve weeks
Secondary Outcomes (2)
Pain measured using a 100mm visual analogue scale.
One, four and twelve weeks
Function of the upper limb measured using the DASH questionnaire.
One, four and twelve weeks
Study Arms (2)
Dorsal block splint
ACTIVE COMPARATORThermoplastic splint in 20 degrees flexion applied to the dorsum of the PIPJ.
Volar gutter splint
EXPERIMENTALThermoplastic splint in 0 degrees flexion applied to the volar surface of the finger.
Interventions
Eligibility Criteria
You may qualify if:
- All stable volar plate injuries.
- Aged 16 and older.
- Male and female.
- Acute presentation within 2 weeks of injury.
- All ethnic groups speaking English.
You may not qualify if:
- Vulnerable patient groups or those lacking capacity.
- Previous injury or pathology involving the same digit.
- Surgical intervention
- Unstable proximal interphalangeal joint.
- Concomitant tendon or additional bony injury outside the traditional Eaton classification types of volar plate injury.
- The DASH outcome measure is available and validated in 27 languages. However, those who do not speak/understand English well will unfortunately be excluded. This is an educational project and therefore there is no funding to use a translator service.
- Volar plate injuries are just as common in children and teenagers as adults. But under 16s will be excluded from this study as the DASH questionnaire has only been assumed valid in adults. There is no research investigating its use in younger age-groups.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- National Health Service, United Kingdomlead
- University of Bradfordcollaborator
Study Sites (1)
Hand Therapy Unit, Mid Yorkshire Hospitals NHS Trust, Pinderfields General Hospital, Aberford Road,
Wakefield, West Yorkshire, WF1 4DG, United Kingdom
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER GOV
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Senior Physiotherapist
Study Record Dates
First Submitted
August 21, 2015
First Posted
August 31, 2015
Study Start
July 1, 2015
Primary Completion
January 1, 2017
Study Completion
January 1, 2017
Last Updated
March 21, 2019
Record last verified: 2019-03