No difference in range of motion at 12 months follow-up
ID
Bron
Verkorte titel
Aandoening
Stiff elbow, Capsule release, Rehabilitation, Continuous Passive Motion, Physical Therapy, Randomized Controlled Trial
Stijve elleboog, kapsel verwijdering, nabehandeling, Continuous Passive Motion, fysiotherapie, Randomized Controlled Trial
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
The primary outcome measure is active and passive ROM (flexion, extension, pronation, supination) of both elbow joints, measured with a universal goniometer, twelve months after surgery.
Achtergrond van het onderzoek
The elbow is prone to stiffness after trauma. To regain functional elbow motion several conservative- and surgical treatment options are available. If conservative treatment fails, an operative release –excision and release of the scarred hypertrophic elbow capsule– of the posttraumatic stiff elbow is often performed. After surgical treatment, several rehab protocols are available, but based on evidence, there is no rehabilitation protocol superior over any of the post-operative treatment options that patients will be assigned to in this study. The following rehab protocols will be compared: 3-day in-hospital regime of CPM with PT versus 3-day in-hospital regime of early motion PT supervised by an upper extremity specialized physical therapist versus outpatient delayed PT supervised by an upper extremity specialized physical therapist from postoperative day 7 as rehabilitation protocol. By conducting this study, we hope to make a statement on the efficacy of costly in-hospital CPM in the treatment of post-operative rehabilitation for patients undergoing surgery for their posttraumatic stiff elbow. Hereby, unnecessary treatment burden for our patients (prolonged hospital stay, and lengthy CPM sessions) as well as redundant costs for society can be avoided, a more universal Evidence-Based method of treatment can be established and the quality of the care can be improved
Doel van het onderzoek
No difference in range of motion at 12 months follow-up
Onderzoeksopzet
Clinical assessment will be performed preoperatively (baseline), during surgery, at day three, at day ten, eight weeks, five months and one year after surgery.
Onderzoeksproduct en/of interventie
Patients that are assigned to the ‘CPM’ group will receive in-hospital CPM in combination with supervised physical therapy the first three days after surgery and supervised physical therapy from day three till day 14 postoperative. Patients that are assigned to the ‘PT’ group will receive in-hospital supervised physical therapy the first three days after surgery and supervised physical therapy from day three till day 14 postoperative. Patients that are assigned to the ‘DPT’ group will receive outpatient physical therapy from postoperative day 7 till 14 and will be discharged from the hospital immediately after surgery. Physical therapy includes both active and passive exercises; moreover patients will be invited to practice at home as well.
Publiek
Jetske Viveen
[default]
The Netherlands
Tel: 0031 614198331
Email: jetskeviveen@gmail.com
Wetenschappelijk
Jetske Viveen
[default]
The Netherlands
Tel: 0031 614198331
Email: jetskeviveen@gmail.com
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Age between 18 and 65 years
Flexion-extension arc of less than 100 degrees or a flexion contracture of more than 30 degrees compared to the contralateral side
Open or arthroscopic surgical treatment received
More than 6 months after trauma
Unsuccessful conservative treatment
Able to read and write in Dutch
Provision of informed consent by patient
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Inflammatory diseases (i.e. rheumatoid arthritis, psoriatic arthritis, or reactive arthritis)
Patients with any other elbow pathology (i.e. spastic contracture)
Neck pain or shoulder pain or other chronic widespread pain syndromes
Abnormalities on the X-ray
Wound problems
Inability to cooperate with a structures rehabilitation protocol
Burn-related contractures
A total elbow or interposition arthroplasty (either planned or in place)
Opzet
Deelname
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Andere (mogelijk minder actuele) registraties in dit register
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In overige registers
Register | ID |
---|---|
NTR-new | NL5792 |
NTR-old | NTR6067 |
CCMO | NL58264.018.16 |
OMON | NL-OMON53066 |