Manual Therapy and Exercise With Mixed Reality With Hololens® Exercise Protocol in Chronic Neck Pain Patiens.

Chronic Pain Clinical Trial

Official title:

Manual Therapy and Exercise With Mixed Reality With Hololens® Exercise Protocol in Chronic Neck Pain Subjects: Clinical Trial

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03903380
• Other study ID #: Holo-CNP
• Status: Terminated
• Phase: N/A
• Start date: April 22, 2019
• Est. completion date: April 1, 2020

Study information

• Verified date: April 2020
• Source: Centro Universitario La Salle
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 14
• Est. completion date: April 1, 2020
• Est. primary completion date: April 1, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

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

Related Conditions & MeSH terms

• Chronic Pain
• Neck Pain

Intervention

Other:
• Manual Therapy and Usual care exercise protocol for neck pain
Manual Therapy protocol between four to eight sessions and exercise protocol will be progressively added to the intervention (from the fouth session of MT approximately).
• Manual Therapy and Augmented reality exercise protocol
Manual Therapy protocol between four to eight sessions and Augmented reality exercise protocol will be progressively added to the intervention (from the fouth session of MT approximately).

Locations

Country	Name	City	State
Spain	IRF La Salle	Madrid	Comunidad De Madrid

Sponsors (2)

Lead Sponsor	Collaborator
Centro Universitario La Salle	Universidad Rey Juan Carlos

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Neck Disability Index (NDI)	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.	change measures (Baseline, 4 weeks)
Primary	Cervical Joint Position Error Test:	This test is used to assess proprioception at the cervical level and the error in joint position sensation	change measures (Baseline, 4 weeks)
Primary	Resistance test of the neck flexor muscles	To perform this test that will give us the resistance in seconds, the therapist lifts	change measures (Baseline, 4 weeks)
Secondary	Tampa Scale for Kinesiophobia(TSK-11)	Self-report that assesses fear related to musculoskeletal pain. It is composed of 11 statements, in which the patient will have to rate from 1 to 4, being 1 totally in disagreement and 4 totally in agreement. The scores will range from 11 to 44 points, the higher the score the greater the fear of pain related to the movement.	change measures (Baseline, 4 weeks)
Secondary	Q Sense (Quantitative termal thresholds: cold and heat)	The thermotest Q-sense evaluates quantitatively the termal thresholds such as cold and heat, as well as the sensation of pain due to heat or cold. It provides an comprehensive somatosensory profile. It has been shown that in patients with sensory disorders of different etiologies, the sensory quantitative tests are considered as an useful/valuable diagnostic tool, which have good interobserver and test-retest reliability	change measures (Baseline, 4 weeks)
Secondary	Pain (VAS)	is a scale of 100 mm, in which the patient must make a mark to indicate the intensity of its pain, being the minimum value 0, which represents the absence of pain and the maximum value is 10, representing the worst pain.	change measures (Baseline, 4 weeks)
Secondary	Evaluation of User Satisfaction with Auxiliary Device Technology (QUEST 2.0)	This consists of 12 questions, each one of which the participant should circle with a circle the number that best describes his or her degree of satisfaction from 1 to 5 (1 being unsatisfied and 5 very satisfied)	change measures (Baseline, 4 weeks)
Secondary	System Usability Scale (SUS)	It consists of 10 questions and the participant should dial the number that best describes their degree of satisfaction from 1 to 5 (1 being unsatisfied and 5 very satisfied)	change measures (Baseline, 4 weeks)