Neck Pain Clinical Trial
— PropNeckPainOfficial title:
Effectiveness of a Propioceptive Exercise Program in Subjects With Inespecific Neck Pain
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 |
Verified date | July 2020 |
Source | University of Valencia |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
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 |
Country | Name | City | State |
---|---|---|---|
Spain | Gemma Victoria Espí-López | Valencia |
Lead Sponsor | Collaborator |
---|---|
University of Valencia |
Spain,
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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