Chronic Pain Clinical Trial
Official title:
Inmediate Effect of the Visualization of Action
Verified date | June 2018 |
Source | Universidad Autonoma de Madrid |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The observation of actions and motor imagery has demonstrated the activation of certain mechanisms similar to those that occur during active movement, which could induce immediate changes in the amplitudes of movement and sensorimotor variables in observed and imagined movements. The main aim of the study was test the immediate effect of a protocol of observed actions and motor imagery on cervical range of motion and pain intensity in patients with non-specific chronic neck pain (NSCNP). Randomized double-blind clinical trial in patients with DCCI at a primary health care center in the Community of Madrid. A random distribution of study subjects was made into two groups: a) cervical motion videos were presented at full range of motion and b) the videos presented showed a range of motion limited to 40%. In both groups, visualization tasks of actions were alternated with internal kinesthetic motor imagery, in periods of 1min in 2 consecutive series and with a total of 12 minutes of intervention. Cervical range of motion was assessed with a cervical goniometer and pain intensity immediately following the intervention with an Analog Visual Scale.
Status | Completed |
Enrollment | 42 |
Est. completion date | April 30, 2018 |
Est. primary completion date | April 30, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility |
Inclusion Criteria: - Nos-Specific Chronic Neck Pain lasting more than 3 months Exclusion Criteria: - Systemic Disease diagnosed (i.e. Lupus, Fibrolyalgia or Rheumatoid Arthritis) - Background of fractures or surgery in the cervical region - congenital anomalies known - infectious processes or diagnosis of active cancer at the time of the study |
Country | Name | City | State |
---|---|---|---|
Spain | CS Entrevías | Madrid |
Lead Sponsor | Collaborator |
---|---|
Universidad Autonoma de Madrid |
Spain,
Eaves DL, Riach M, Holmes PS, Wright DJ. Motor Imagery during Action Observation: A Brief Review of Evidence, Theory and Future Research Opportunities. Front Neurosci. 2016 Nov 21;10:514. eCollection 2016. Review. — View Citation
Mao C, Wei L, Zhang Q, Liao X, Yang X, Zhang M. Differences in brain structure in patients with distinct sites of chronic pain: A voxel-based morphometric analysis. Neural Regen Res. 2013 Nov 15;8(32):2981-90. doi: 10.3969/j.issn.1673-5374.2013.32.001. — View Citation
Muñoz-García D, Gil-Martínez A, López-López A, Lopez-de-Uralde-Villanueva I, La Touche R, Fernández-Carnero J. Chronic Neck Pain and Cervico-Craniofacial Pain Patients Express Similar Levels of Neck Pain-Related Disability, Pain Catastrophizing, and Cervical Range of Motion. Pain Res Treat. 2016;2016:7296032. doi: 10.1155/2016/7296032. Epub 2016 Mar 29. — View Citation
Niddam DM, Lee SH, Su YT, Chan RC. Brain structural changes in patients with chronic myofascial pain. Eur J Pain. 2017 Jan;21(1):148-158. doi: 10.1002/ejp.911. Epub 2016 Jun 28. — View Citation
van Hecke O, Torrance N, Smith BH. Chronic pain epidemiology and its clinical relevance. Br J Anaesth. 2013 Jul;111(1):13-8. doi: 10.1093/bja/aet123. Review. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Cervical Range of Movement | CROM goniometer | at the beginning and after the intervention, until the end of the study (24 hours) | |
Secondary | Cervical Pain Disability | Neck Disability Index | at the beginning and end of the intervention, until the end of the study (24 hours) | |
Secondary | Pain Intensity | Visual Ananlogue Scale: 10cm line, were the left limit means "no pain" and the right limit means "worst imaginable pain" | at the beginning and end of the intervention, until the end of the study (24 hours) | |
Secondary | Catastrophizism | Pain Catastrophizing Scale | at the beginning and end of the intervention, until the end of the study (24 hours) | |
Secondary | Health Related Quality of Life | EuroQoL-5D-5L | at the beginning and end of the intervention, until the end of the study (24 hours) | |
Secondary | Anxiety and Depression | Hospital Anxiety and Depression Scale (HADs) | at the beginning and end of the intervention, until the end of the study (24 hours) |
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