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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03218644
Other study ID # ID0017
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 14, 2017
Est. completion date August 15, 2017

Study information

Verified date July 2020
Source University of Valencia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Introduction: Neck pain is among the most common and costly for industrialized societies. It is difficult to know the exact structure causing the pain so most are considered as non-specific neck pain. There is a correlation between the alteration of craneocervical proprioception and neck pain. The evidence for treatment with proprioceptive exercises is very limited.

Objective: To know the efficacy of a proprioceptive exercise program for neck pain and to compare its effects with a cervical mobility program.

Materials and Methods: Subjects between 18-65 years old with non-traumatic neck pain are included. They will be randomized into two groups of exercises: proprioception or mobility, which will be developed over a period of two weeks, every day, with a total of 10 sessions per patient.


Recruitment information / eligibility

Status Completed
Enrollment 47
Est. completion date August 15, 2017
Est. primary completion date August 15, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Neck pain (NAD I-II) of recent onset (0-3 months)

Exclusion Criteria:

- Cognitive difficulties

- Lack of commitment to attend sessions

- Subjects with pacemakers or defibrillators

- Being receiving another physiotherapeutic treatment

- Other pathologies

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Mobility exercises
Usual treatment and exercises of cervical mobility before a mirror.
Proprioception exercises
proprioceptive exercises for craniocervical sensorimotor control.

Locations

Country Name City State
Spain Gemma Victoria Espí-López Valencia

Sponsors (1)

Lead Sponsor Collaborator
University of Valencia

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Intensity of Pain Visual Analogue Scale (VAS) was used to register the pain. The VAS is a 10-point rating scale. four weeks
Secondary Head Repositioning Test The cervical position is reevaluated with a laser pointer. four weeks
Secondary Cervical movement range (CROM) Evaluated with cervical goniometer. four weeks
Secondary Pain points Algometer four weeks
Secondary Neck Disability Neck Disability Index four weeks
Secondary Health status Evaluated with questionnaire of Quality of life four weeks
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