"Evidence of the Use of Virtual Reality Versus Manual Therapy and Therapeutic Exercise in Rotator Cuff Injury"
- Conditions
- Rotator Cuff Injuries
- Interventions
- Other: manual therapy and therapeutic exerciseOther: manual therapy and therapeutic exercise and virtual reality
- Registration Number
- NCT06482255
- Lead Sponsor
- University of Alcala
- Brief Summary
This study evaluates the effectiveness of virtual reality (VR) compared to manual therapy and therapeutic exercise in treating rotator cuff injuries. It involves 108 participants divided into two groups: one receiving VR combined with manual therapy and therapeutic exercise, and the other receiving only manual therapy and therapeutic exercise. The study spans 10 weeks, with assessments at the beginning, midpoint, and end. Variables measured include quality of life, perceived pain, shoulder disability, strength, pain intensity, and shoulder mobility. The aim is to determine if VR provides better outcomes in these variables compared to conventional treatments.
- Detailed Description
Introduction Background: The shoulder is one of the most mobile yet unstable joints in the human body, making it prone to injuries like tendinopathies, which are among the most disabling injuries in the upper limb. Rotator cuff injuries are particularly prevalent.
Rotator Cuff: Comprises the supraspinatus, infraspinatus, subscapularis, and teres minor muscles, which provide stability, strength, and movement to the shoulder joint.
Treatment Options: There are conventional (non-surgical) and surgical treatments for rotator cuff injuries. Conventional treatments are often preferred due to fewer complications and lower costs.
Study Objective The study aims to assess the effectiveness of VR in comparison with traditional manual therapy and therapeutic exercise for treating rotator cuff injuries. The goal is to see if integrating VR can enhance patient outcomes.
Methodology Participants: 108 individuals will be recruited and divided into two groups. Group 1: Will receive a combination of VR, manual therapy, and therapeutic exercise.
Group 2: Will receive only manual therapy and therapeutic exercise. Duration: The treatment will last for 10 weeks.
Measurements: The study will measure various outcomes, including:
Quality of Life: Assessed using the SF-36 questionnaire. Perceived Pain and Shoulder Disability: Measured with the SPADI questionnaire. Strength: Evaluated using dynamometry. Pain Intensity: Assessed with the Numerical Rating Scale (NRS). Active Shoulder Mobility: Measured using an inclinometer. Assessment Points: Measurements will be taken before treatment, at the midpoint (5 weeks), and at the end of the treatment (10 weeks).
Data Collection and Analysis Data on pain, disability, strength, and range of motion will be collected at three intervals: pre-treatment, 5 weeks, and 10 weeks.
Quality of life will be assessed at the beginning and end of the treatment. Statistical Analysis: Using SPSS version 29.0, descriptive and inferential statistics will be conducted to analyze the data. An ANOVA will be used to study the treatment effects, considering group and time as factors.
Limitations Population Characteristics: The specific demographic characteristics of the study population might limit the generalizability of the results.
Lack of 3D Kinetic Evaluation: The absence of a three-dimensional kinetic evaluation protocol for scapular dyskinesia is noted as a limitation.
Cost of VR Technology: The expense associated with VR technology is highlighted as a limitation since it is still a growing and costly field.
Conclusion The study seeks to provide evidence on whether VR can be an effective tool alongside traditional therapies for rotator cuff injuries, potentially offering new avenues for rehabilitation practices.
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Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 108
- be between 18 and 65 years old
- have a rotator cuff injury lasting less than 3 months
- have a limitation in strength of less than 30%
- pain in mobility greater than 4/10
- previous shoulder surgeries, medical pathologies such as cancer
- rheumatoid disease, infections and/or fractures, and CNS involvement.
- In addition, physiotherapy treatment different from that of the study and not having an understanding of the Spanish language will be cause for exclusion.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description manual therapy and therapeutic exercise manual therapy and therapeutic exercise * Soft tissue massage * Mobilization of the glenohumeral joint * Scapular retraining virtual reality and manual therapy and therapeutic exercise manual therapy and therapeutic exercise and virtual reality * Soft tissue massage * Mobilization of the glenohumeral joint * Scapular retraining Therapeutic Exercise
- Primary Outcome Measures
Name Time Method Perceived pain and disability regarding the shoulder 10 weeks continuous metric quantitative variable. To measure it the investigators will use the SPADI questionnaire that takes values from or to 10 in each question. Reliability is greater than 0.7, with ranges between 0.7 and 0.9
strength 10 weeks continuous metric quantitative variable and the investigators will measure it using the dynamometer. It has a reliability of 0.90%, making it a useful force measurement instrument.
Active shoulder mobility 10 weeks continuous metric quantitative variable. The investigators will use an inclinometer to assess flexion, extension, rotation, abduction and adduction.
- Secondary Outcome Measures
Name Time Method