This study will compare functional outcomes after an arthroscopic Bankart repair between patients that underwent conventional arthroscopic Bankart repair rehabilitation, following the American Society of Shoulder and Elbow Therapists guideline and patients that underwent 'multifactorial approach training', which focusses on decreasing kinesiophobia and fear of recurrent dislocations. The study population comprises patients who will undergo Arthroscopic Bankart Repair (ABR) after a traumatic anterior shoulder dislocation at Spaarne Gasthuis Haarlem/Hoofddorp, OLVG Amsterdam, Amstelland Ziekenhuis Amstelveen, Gelre Ziekenhuizen, Medisch Spectrum Twente, or Flevoziekenhuis Almere.
Background: Fear for (recurrent) dislocation is a frequently reported patient perception regarding the treatment of anterior shoulder instability and is associated with poor outcomes like decrease in quality of life and unsuccesful return to sport. There is lack of standard multifactorial aftercare of shoulder instability surgery incorporating the psychological component of the experiences trauma of patients with shoulder instability. Therefore, a newly developed Rehabilitation Protocol (REPRO) aims to reduce fear for dislocation in order to increase psychological readiness to return to sport. The aim of this study is to compare the effect on the psychological readiness to return to sport between our new Multifactorial Approach Training (MAT) and Conventional Arthroscopic Bankart Repair Rehabilitation (CABRR) in a single-blinded, multi-center randomized controlled trial. Methods: Patients, aged 18-67 years, with traumatic anterior shoulder instability, undergoing ABR will be included. Rehabilitation is started within 4 weeks following surgical treatment. Patients will be randomized to either the control group (A) or the MAT group (B). Group A will receive CABRR, according to the American Society of Shoulder and Elbow Therapists (ASSET) guidelines. Group B will receive MAT, following the REPRO. A total of 92 patients will be included, with 46 patients per study arm. Patients will be followed-up for 52 weeks. The primary outcome is change from baseline (surgical intervention; ABR) in Shoulder Instability Return to Sport Index (SIRSI) at 26 weeks postoperatively. Secondary outcomes include Oxford Shoulder Instability Score (OSIS), Subjective Shoulder Value (SSV), fear for dislocation measured with a Numeric Rating Scale (NRS), Tampa Scale of Kinesiophobia in patients with Shoulder Instability (TSK-SI), World Health Organization Quality of Life Questionnaire - BREF (WHOQoL-BREF), Return To Work (RTW), Return To Sports (RTS), shoulder pain measured with a NRS, , number of physiotherapy and outpatient clinic visits and patient satisfaction (VAS). At baseline and at 26 weeks postoperatively patients will undergo a task-based brain activity analysis using functional Magnetic Resonance Imaging (fMRI) to determine functional cerebral changes after treatment. The MATASI trial is to be conducted between 2024 and 2026.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
100
The protocol consists of four phases: 1) immobilization phase, 2) early protective phase, 3) intermediate phase and 4) late phase. The detailed guideline can be found in the following article: Gaunt, B. W., Shaffer, M. A., Sauers, E. L., Michener, L. A., McCluskey, G. M., \& Thigpen, C. A. (2010). The American Society of Shoulder and Elbow Therapists' Consensus Rehabilitation Guideline for Arthroscopic Anterior Capsulolabral Repair of the Shoulder. Journal of Orthopaedic \& Sports Physical Therapy, 40(3), 155-168. https://doi.org/10.2519/jospt.2010.3186
The protocol consists of four phases: 1) immobilization phase, 2) early phase, 3) intermediate phase and 4) advanced phase. The protocol comprises education, modified cognitive behavioral therapy, neuromuscular control exercises, kinetic chain exercises, range of motion enhancing exercises, strength and conditioning exercises, and sport-specific exercises. The protocol is currently unpublished.
Shoulder Instability Return to Sport Index (SIRSI)
Patient reported outcome measure to assess psychological readiness to return to sport in patients with shoulder instability
Time frame: 26 weeks postoperative
Oxford Shoulder Instability Score (OSIS)
Patient reported shoulder function between MAT and CABRR
Time frame: 26 and 52 weeks postoperative
Shoulder function, measured by Subjective Shoulder value (SSV)
Shoulder function, measured by Subjective Shoulder value (SSV)
Time frame: baseline, 26 and 52 weeks postoperative
Fear of recurrent dislocation, measured by Numeric Rating Scale (NRS)
Fear of recurrent dislocation, measured by Numeric Rating Scale (NRS)
Time frame: baseline, 26 and 52 weeks postoperative
Tampa Scale for Kinesiophobia in patients with Shoulder Instability (TSK-SI)
Patient reported outcome measure to assess the degree of kinesiophobia
Time frame: baseline, 26 and 52 weeks postoperative
World Health Organization Qualitiy of Life Questionnaire - BREF (WHOQoL-BREF)
Patient reported outcome measure to assess the self reported quality of life
Time frame: baseline, 26 and 52 weeks postoperative
Level of shoulder pain measured by Visual Analogue Scale (VAS)
Level of shoulder pain measured by Visual Analogue Scale (VAS)
Time frame: baseline, 26 and 52 weeks postoperative
Number of patients that return to work (RTW) following the surgery
Number of patients that return to work (RTW) following the surgery
Time frame: 26 and 52 weeks postoperative
Number of patients tha return to sport (RTS) following the surgery
Number of patients tha return to sport (RTS) following the surgery
Time frame: 26 and 52 weeks postoperative
Patient satisfaction regarding the surgical treatment and rehabilitation, measured by VAS
Patient satisfaction regarding the surgical treatment and rehabilitation, measured by VAS
Time frame: baseline, 26 weeks and 52 weeks postoperative
The number of physiotherapy and orthopedic surgeon visits
The number of physiotherapy and orthopedic surgeon visits
Time frame: From start to end of treatment
Task-based brain activity, measured in voxels
Analysis using functional Magnetic Resonance Imaging (fMRI) to determine functional cerebral changes after treatment
Time frame: baseline and 26 weeks postoperative
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