About this trial
Kinesiophobia (fear of physical movement) is common after a previous shoulder dislocation and persists after one year, regardless of the occurrence of a recurrence. This kinesiophobia is associated with a lower level of physical activity and a lower return to sport. Increased kinesiophobia, combined with other psychological factors such as depression and fear of re-injury in patients with shoulder instability, results in poor outcomes after treatment. Given that there is currently no postoperative protocol that takes this psychological component into account, a new rehabilitation protocol focused on reducing kinesiophobia was recently designed as part of an international consensus study based on the method Delphi. This protocol includes a core set of evidence-based interventions aimed at regaining functional stability of the shoulder and reducing fear of recurrent dislocation and kinesiophobia. The goal of this study is to determine if we can reduce kinesiophobia in patients who have undergone stabilization surgery for anterior shoulder instability using this new rehabilitation protocol.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Primary or recurrent traumatic anterior dislocation of the shoulder
Indication of abutment according to Latarjet (arthroscopic or open sky)
Age: 18-67 years
Understanding of the French language spoken and written
Disqualifiers
Posterior or multidirectional instability of the shoulder (Beighton score >5)
Age <18 or >67 years.
Patients with additional rotator cuff tear.
Patients with a history of surgery on either shoulder.
Trial design
Parallel
Treatments tested in this trial
consultations with a psychologist
Other interventionConsultations with a sports psychologist to decrease kinesiophobia
Conventional reeducation
Other interventionConventional reeducation
Treatment groups
Trial outcomes
Primary outcomes
Western Ontario Shoulder Instability Index (WOSI)
self-evaluating shoulder instability quality of life score : 21 items. The patient is asked to grade the function of a specific item on a horizontal visual analog scale from 0 to 100 mm. Each question results in a number between 0 and 100 and the total score may be presented as a number between 0 and 2,100 points (where 0 represents no deficit and 2,100 the worst)
Secondary outcomes
Shoulder subjective value
subjective evaluation by the patient of shoulder function, expressed as a percentage of a normal shoulder. This score ranges from 0 to 100%.
ability to return to work
time indication
ability to return to sport
time indication
Patient's pain
visual analogic scale between 0 and 10
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