beta
Trial Radar AI
Clinical Trial NCT06963983 for Shoulder Instability, Frozen Shoulder, Rotator Cuff Tears is recruiting. See the Trial Radar Card View and AI discovery tools for all the details. Or ask anything here.
One study matched filter criteria
Card View
Back to Search

Virtual Reality Rehabilitation for Shoulder Pathologies 15 Exercise-Based Virtual

Recruiting
Clinical Trial NCT06963983 is an interventional study for Shoulder Instability, Frozen Shoulder, Rotator Cuff Tears that is recruiting. It started on 28 October 2024 with plans to enroll 15 participants. Led by La Tour Hospital, it is expected to complete by 28 June 2025. The latest data from ClinicalTrials.gov was last updated on 9 May 2025.
Brief Summary
Most rehabilitation protocols require patients to train the affected limbs with high regularity, following repetitive cycles of exercises, in order to recover mobility and strength. Nonetheless, the repetitive nature of these exercises can demotivate patients leading to less intense and committed training, if not ending with a lack of compliance toward the prescribed exercises, ultimately leading to a suboptimal reco...Show More
Official Title

Personalized Rehabilitation System Using Gamification With Virtual Reality Technology: A Feasibility Study

Conditions
Shoulder InstabilityFrozen ShoulderRotator Cuff Tears
Other Study IDs
  • 2022-00166
NCT ID Number
NCT06963983
Start Date (Actual)
2024-10-28
Last Update Posted
2025-05-09
Completion Date (Estimated)
2025-06-28
Enrollment (Estimated)
15
Study Type
Interventional
PHASE
N/A
Status
Recruiting
Primary Purpose
Treatment
Design Allocation
N/A
Interventional Model
Single Group
Masking
None (Open Label)
Arms / Interventions
Participant Group/ArmIntervention/Treatment
ExperimentalShoulder Pathology Group
Patients suffering from either shoulder instability, frozen shoulder or rotator cuff tears
Rehabilitation using virtual reality
During the four physiotherapy (PT) sessions (60 min for each session), a set of exercises from the conventional PT is replaced by multiple short sessions of 30 minutes each, where the patient will be equipped by a set of motion trackers mounted on a belt and on a set of straps to be worn around both arms and both forearms. The patient will also hold a controller in each hand and wear a commercial VR headset on his he...Show More
Primary Outcome Measures
Outcome MeasureMeasure DescriptionTime Frame
Simulator Sickness Questionnaire
From 1 (best) to 7 (worst)
Day 1
Secondary Outcome Measures
Outcome MeasureMeasure DescriptionTime Frame
A reduced version of the Post-experimental Intrinsic Motivation Inventory
From 1 (worst) to 7 (best)
Day 1
A reduced version of the Avatar Embodiment Questionnaire
From 1 (worst) to 7 (best)
Day 1
Patient satisfaction
4-Point Likert Scale (Not satisfied at all, Not satisfied, Satisfied, Very satisfied)
Day 1
Participation Assistant
Eligibility Criteria

Eligible Ages
Adult, Older Adult
Minimum Age
18 Years
Eligible Sexes
All
  • Adult patients able to understand the content of the patient information / consent form and give consent to take part in the research project
  • Glenohumeral instability surgical treated with traumatic initial instability in a < 20 years old athlete, recurrent instability with one or more of the following criteria: a failure of conservative treatment, locked dislocation, failed prior surgery, high risk for further recurrence (i.e. collision or competitive athletes), Critical glenoid bone-loss (>15-20%), bipolar bone-loss resulting in "off-track" lesion
  • Partial or complete rotator cuff repair with an indication to postoperative rehabilitation depending on surgeon recommendation
  • Idiopathic, primary, or secondary frozen shoulder

  • Patients with a language barrier hindering questionnaires completion
  • Patients unlikely to attend clinical follow-up (e.g. when living abroad)
  • Legal incompetence
  • Enrolment of the investigators, his/her family members, employees and other dependent persons
  • Non-motivated patients
  • Active infection
  • Exclusion criteria related to glenohumeral instability: uncontrolled epilepsy, spontaneous unidirectional instability in a hyperlax patient, multidirectional instability, elher-Danlos syndrome
  • Exclusion criteria related to rotator cuff tears: Additional procedure(s) (muscle transfer, patch,…)
  • Exclusion criteria related to VR use: Patients with a predisposition to motion sickness, Patients suffering from epilepsy or having any serious mental illness (schyzophrenia, neurological problems, etc.), Patients with visual impairment , Patients will intellectual disability that prevent them to understand how to use the VR rehabilitation system, Patients with bilateral upper limb injuries, as one side is needed as healthy reference
La Tour Hospital logoLa Tour Hospital
Study Responsible Party
Dr. Alexandre Lädermann, Principal Investigator, Orthopaedic surgeon, La Tour Hospital
Study Central Contact
Contact: Alexandre Lädermann, MD, +41 22 719 75 55, [email protected]
1 Study Locations in 1 Countries

Canton of Geneva

La Tour hospital, Meyrin, Canton of Geneva, 1217, Switzerland
Hugo Bothorel, MEng, Contact, +41 22 719 78 33, [email protected]
Recruiting