Pain, Neck Clinical Trial
Official title:
Evaluation of Nociceptive Processing in the Cervical Region Through Action Observation, Laterality Discrimination and Exercise
Verified date | January 2020 |
Source | Universidad Rey Juan Carlos |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The main objective of this research is to asses the effectivity of action observation therapy, left/right discrimination and therapeutic exercise in the nociceptive processing of the cervical region.
Status | Completed |
Enrollment | 54 |
Est. completion date | December 30, 2019 |
Est. primary completion date | July 30, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Healthy volunteers. - Asymptomatic on cervical region. - Understands and accept the informed consent. - Spanish speakers. - People with no cognitive disorders. Exclusion Criteria: - Pregnant women. - Positive neurological signs or evidence of spinal cord compression (abnormal diffuse sensitivity, hyperreflexia or diffuse weakness). - Previous cervical surgeries with recurrent symptoms. - Previous headaches. - Inability to provide informed consent. - Cognitive disorders. - Reading or verbal misunderstanding when receiving instructions. - Having suffered any pain in the last 3 months, both in the quadrant suppressor as in the lumbar region and pelvis. - Suffer any pain at the time of the study. - Any recent traumatic event, whether physical or psychological / emotional. |
Country | Name | City | State |
---|---|---|---|
Spain | Universidad Rey Juan Carlos | Alcorcon | Madrid |
Spain | Centro superior de Estudios Universitarios La Salle | Madrid | Aravaca |
Lead Sponsor | Collaborator |
---|---|
Josue Fernandez Carnero | Centro Universitario La Salle |
Spain,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Physical activity of the patients. | International physical activity questionnaire. Results are reported in categories depending on the variable 'MET minutes a week'. MET minutes represent the amount of energy expended carrying out physical activity. High physical activity (one hour of more of physical activity per day), moderate physical activity (half an hour of physical activity per day) or low physical activity (not meeting any of the criteria for either moderate or high levels of physical activity). | Before and after the treatment (2 weeks), after 15 days and after 30 days. | |
Primary | Changes in cervical range of movement. | Measured with goniometer by the physiotherapists. | Before and after the treatment (2 weeks), after 15 days and after 30 days. | |
Primary | Changes in pain perception. | Self reported Visual Analog Scale. Minimum value is 0 (best); Maximun value is 10 (worst). | Before and after the treatment (2 weeks), after 15 days and after 30 days. | |
Primary | Changes in the subject's selective attention capacity and skills as well as their processing speed ability. | It will be measured using the Encephalapp application. The time taken to perform 2 successful trials of 10 images without making an error was recorded. | Before and after the treatment (2 weeks), after 15 days and after 30 days. | |
Primary | Changes in pain treshold perception. | Mechanical nociceptive threshold test using Von-Frey filaments. | Before and after the treatment (2 weeks), after 15 days and after 30 days. | |
Primary | Changes in upper Limb Neurodinamics. | Upper limb neurodinamics test measuring with a goniometer on what grade of joint movement with nerve stretching pain appears. | Before and after the treatment (2 weeks), after 15 days and after 30 days. | |
Primary | Changes in levels of hyperalgesia to pressure and maximum pressure tolerance. | Pressure Pain Tresholds using an algometer on first finger, trapezius muscle and tibia. | Before and after the treatment (2 weeks), after 15 days and after 30 days. | |
Primary | Changes in endogenous pain inhibition mechanisms. | Conditioned pain modulation and temporal summation (windup), using the algometer and an oclussion band. | Before and after the treatment (2 weeks), after 15 days and after 30 days. | |
Primary | Changes in pain to cold threshold. | Cold stimulation test using cold compresses on the cervical region two times during 10 minutes. | Before and after the treatment (2 weeks), after 15 days and after 30 days. | |
Primary | Changes in deep neck flexors activation. | Deep neck flexor endurance test. | Before and after the treatment (2 weeks), after 15 days and after 30 days. | |
Primary | Changes in hand and forearm muscular strenght. | Handgrip strenght test using a dynamometer. | Before and after the treatment (2 weeks), after 15 days and after 30 days. | |
Secondary | Changes in levels of Catastrophism. | 13 item Pain Catastrophic Scale that must be answered with a numeric value between 0 (not at all) and 4 (all the time), with a maximum score of 52 points, with higher scores indicating greater pain catastrophizing. | Before and after the treatment (2 weeks), after 15 days and after 30 days. | |
Secondary | Changes in Kinesiophobia, levels of fear to movement. | 11 item Tampa Scale for Kinesiophobia, the final score can range between 11 and 44 points, with higher scores indicating greater perceived kinesiophobia. | Before and after the treatment (2 weeks), after 15 days and after 30 days. | |
Secondary | Changes in Fear-avoidance behaviours. | Fear-avoidance Beliefs Questionnaire . The instrument consists of two subscales, a four-item physical activity subscale, and a seven-item work subscale. Each item is scored from 0 to 6 and summed to produce the subscale score. Possible scores range from 0-28 to 0-42, with higher scores indicating greater fear avoidance beliefs. | Before and after the treatment (2 weeks), after 15 days and after 30 days. | |
Secondary | Changes in level of Depression. | Beck's Depression Inventory II is a 21-item self-reporting questionnaire. It scores from 0 to 21, the higher is the score the higher is the level of depression. | Before and after the treatment (2 weeks), after 15 days and after 30 days. | |
Secondary | Changes in patient's anxiety. | State-Trait Anxiety Inventory. The total score ranges from 0-63 interpreted as follows: 0-9, normal or no anxiety; 10-18, mild to moderate anxiety; 19-29, moderate to severe anxiety; and 30-63, severe anxiety. | Before and after the treatment (2 weeks), after 15 days and after 30 days. | |
Secondary | Changes in the ability to generate mental motor images. | The Movement Imagery Questionnaire-Revised. It is an 8-item self-reporting inventory rating the difficulty of generating that image on a 7-point scale, where 1 indicates 'very difficult to see/feel' and 7 indicates 'very easy to see/feel'. | Before and after the treatment (2 weeks), after 15 days and after 30 days. |
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