Manual Therapy and Exercise With Mixed Reality With Hololens® Exercise Protocol in Chronic Neck Pain Subjects: Clinical Trial
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Neck Pain
- Sponsor
- Centro Universitario La Salle
- Enrollment
- 14
- Locations
- 1
- Primary Endpoint
- Neck Disability Index (NDI)
- Status
- Terminated
- Last Updated
- 6 years ago
Overview
Brief Summary
Currently, cervical pain is the second most frequent musculoskeletal disorder, which generates an important impact on the function and quality of life. It is estimated that its anual prevalence for the general population can reach 50%.
Non-specific cervical pain attends without signs or symptoms of structural or neurological pathology, its etiology is unknown. However, it is related with joint and muscular structures. It has been observed a decrease in the strength and endurace of the deep cervical flexor muscles in 70% of patients with cervical pain; as well as motor control déficit and coordination alterations in the sinergy between the activity of the superficial and deep musculature.
Also, phycosocial factors, as for example: behaviors of fear-avoidance, catastrophism, hypervigilancy, psychosocial stress and negative adaptative neuroplastic changes, may have an importante role in chronic musculoskeletal pain.
In the last years, RV has been used in clinical rehabilitation, being a reliable and valid tool, which allows the patient distration to virtual world and they have offered results like: decreased pain and fear of movement and also improvements in motor performance and neuroplasticity processes.
The aim of this single-blinded randomized novel pilot study is to observe the effects generated in motor variables, when a protocol of manual therapy combined with augmented reality as a method of exercise in subjects with non-specific cervical pain is applied; in comparaison with a protocol of manual therapy combined with conventional cervical exercises.
Different variables will be measured at the beginning and at the end of intervention. Also, they will be measured one month after the intervention to observe the changes produced in short term. These variables are: pain, function, satisfaction, propioception, endurance, as well as phychological and somatosensory variables.
Investigators
Hector Beltran-Alacreu
Principal Investigator
Centro Universitario La Salle
Eligibility Criteria
Inclusion Criteria
- •- Men and women.
- •Age: 18-65 years old.
- •Persistent neck pain for at least 3 month or intermittent neck pain for 6 month or more.
- •5 points or 10% at the Neck Disability Index questionnaire.
Exclusion Criteria
- •Cervical whiplash (10 years before)
- •Cervical fractures.
- •Vestibular pathology.
- •Epilepsy or other neurological condition.
- •Systemic diseases.
- •Cardiovascular or respiratory disorders that affect physical performance.
- •Lasik eye surgery.
- •Fibromyalgia
- •Pregnancy
Outcomes
Primary Outcomes
Neck Disability Index (NDI)
Time Frame: change measures (Baseline, 4 weeks)
A self-completed questionnaire based on Owestry Scale for low back pain. It is one of the most used questionnaires in the evaluation of cervical pain. Evaluates the disability level.
Cervical Joint Position Error Test:
Time Frame: change measures (Baseline, 4 weeks)
This test is used to assess proprioception at the cervical level and the error in joint position sensation
Resistance test of the neck flexor muscles
Time Frame: change measures (Baseline, 4 weeks)
To perform this test that will give us the resistance in seconds, the therapist lifts
Secondary Outcomes
- Evaluation of User Satisfaction with Auxiliary Device Technology (QUEST 2.0)(change measures (Baseline, 4 weeks))
- Tampa Scale for Kinesiophobia(TSK-11)(change measures (Baseline, 4 weeks))
- System Usability Scale (SUS)(change measures (Baseline, 4 weeks))
- Q Sense (Quantitative termal thresholds: cold and heat)(change measures (Baseline, 4 weeks))
- Pain (VAS)(change measures (Baseline, 4 weeks))