Interdisciplinary treatment following hyperextension trauma of the finger.

Interdisciplinary treatment following proximal interphalangeal joint (PIPJ) dislocation or hyperextension trauma of the finger: feasibility study.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON21696

Enrollment

Registered

2017-05-26

Start date

2017-06-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

1)Health condition: volar plate lesion, PIPJ dislocation, hyperextension trauma 2)Problem studied: a)The feasibility of the new developed protocol, after PIPJ dislocation regarding: - Equipment - Procedure - Integrated co-ordination of the treatment between the primary care specialist, the hand-surgeon and the hand therapist. b) Potential benefit of the protocol in patients with PIPJ dislocation problems, regarding: - function, activity and participation level.

Interventions

Participants after PIPJ-dislocation will follow the new structured interdisciplinary treatment protocol, based on existing conservative treatment approaches, to evaluate this process with experts and

Eligibility

Inclusion criteria

Inclusion criteria: - PIPJ-dislocation - Volar plate lesion - Hyperextension trauma - Clinically diagnosed with x-ray: - Avulsion fracture less than 30-40% of the joint surface. - Age: > 18 years - Post-injury time of 0-3 weeks (acute group) - Ability to understand the Dutch language.

Exclusion criteria

Exclusion criteria: - Avulsion fracture more than 40 % of the joint surface. - Surgical indication of the PIP-joint - Post-injury time more than 3 weeks (sub-acute of chronical group) - Other pathology: acute complex regional pain syndrome (CRPS), inflammatory arthritic conditions, or artificial joints

Design outcomes

Primary

Measure	Time frame
The specialist and therapeutic experiences regarding: - the interdisciplinary collaboration, - the equipment used, - the procedure including timing and frequency of measurements.	—

Secondary

Measure	Time frame
The 'order of magnitude' of the potential benefit of the protocol in patients with PIPJ dislocation problems, the following outcome measures will be described: the parameters of function, activity and participation level of the patient. The parameters include the active range of motion (AROM), pain using the numeric pain rating scale (NPRS) and scores of the Quick Dash and the Jamar dynamometer for grip strength.	—

Measure

Time frame

The 'order of magnitude' of the potential benefit of the protocol in patients with PIPJ dislocation problems, the following outcome measures will be described: the parameters of function, activity and participation level of the patient. The parameters include the active range of motion (AROM), pain using the numeric pain rating scale (NPRS) and scores of the Quick Dash and the Jamar dynamometer for grip strength.

—

Contacts

Public ContactN.K. Breuer

Afdeling Revalidatie, Zuyderland Medisch Centrum Heerlen

n.breuer@zuyderland.nl045/5766635

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)