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NCT02553759 Clinical Trial

Observed Actions in Chronic Neck Pain

Chronic Pain Clinical Trial

— ObACNPain  

Official title:
Influence of the Actions Observed on Cervical Motion in Patients With Chronic Neck Pain. Randomized Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02553759
Other study ID # ObActions
Secondary ID
Status Completed
Phase N/A
First received September 16, 2015
Last updated September 17, 2015
Start date October 2013
Est. completion date May 2015

Study information
Verified date September 2015
Source AG Clinic
Contact n/a
Is FDA regulated No
Health authority Spain: Comité Ético de Investigación Clínica
Study type Interventional

Clinical Trial Summary

The aim of the present protocol is to prove if the observed actions (AOb) will improve the cervical range of motion (CROM) in patients with non-specific chronic neck pain (CNP). This study is a parallel-group double blind randomized clinical. Outcome measures were CROM, and pressure pain detection thresholds (PPDT) with a digital algometer. The follow-up will consist of three evaluations: pre- treatment, post-treatment and 10 minutes after second measurement (motor imagery).

Recruitment information / eligibility
Status Completed
Enrollment 28
Est. completion date May 2015
Est. primary completion date June 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Non specific chronic neck pain

- Diagnosed by medical specialist

Exclusion Criteria:

- cervical osteoarthritis or polyarthrosis

- rheumatic disease

- history of cervical hernia

- whiplash syndrome

- surgery on the neck, face or shoulders,

- systemic disease, medical history of cancer

- significant trauma that the patient relates to their pain and/or refusal to participate

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Other:
• Actions observed
Patients observed movements without realize them. After this actions, movements will be imagined by patients

Locations
Country Name City State
n/a

Sponsors (2)
Lead Sponsor Collaborator
AG Clinic Hospital Universitario La Paz

Outcome
Type Measure Description Time frame Safety issue
Primary Range of motion degrees 10 minutes No
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