Cervical Spine Osteophyte Clinical Trial
— PNFOfficial title:
Effect of Chosen Treatment Methods on Pain, ROM, Associated Symptoms and Functioning in Patients With Cervical Spine Osteoarthritis: Randomised Control Trial
NCT number | NCT03683602 |
Other study ID # | NECK/2018 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | January 2011 |
Est. completion date | April 2014 |
Verified date | September 2018 |
Source | Jagiellonian University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Abstract Objective: To compare effect of PNF therapy with manual therapy on pain, associated
symptoms, range of motion and functioning in patients with cervical spine osteoarthritis.
Design: Parallel group, single-center, double-blinded randomized controlled trial.
Setting: Outpatient clinic in hospital KCRiO. Subject: Eligible patients were female adults
with chronic pain of cervical spine due to osteoarthritis of vertebral body and
intervertebral disc confirmed by X-ray.
Interventions: Group I (PNF group) was treated according to PNF concept, while Group II
according to manual therapy (manual therapy group). Both groups received 10 days of
treatment, 45 minutes each day.
Main measures: Primary outcomes measures were Oswestry scale and range of motion (ROM).
Secondary outcomes measures were subjective evaluation of cervical pain according to VAS
scale and associated symptoms (headache, vertigo, ROM of shoulder joints, balance). For each
scale results were measured at baseline, after two weeks of intervention and after a
three-month follow-up period without therapy.
Keywords: neck pain, PNF, manual therapy
Status | Completed |
Enrollment | 80 |
Est. completion date | April 2014 |
Est. primary completion date | April 2013 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 45 Years to 65 Years |
Eligibility |
Inclusion criteria: - age 45-65, - female gender, - cervical pain due to osteoarthritis of vertebral body and intervertebral disc confirmed by X-ray, - chronic pain lasting more than 13 weeks, verbal contact, - intact cognitive functions and voluntary consent for the study. Exclusion criteria - birth or aquired deficits, - cervical spine injury, - osteoporosis, - cervical spine instability, - myelopathy, - signs of nerve root compression of C1-C8, such as paresis, muscle loss, hyporeflexia, use of analgesics, - anti-inflammatory drugs or myorelaxants. |
Country | Name | City | State |
---|---|---|---|
Poland | Krakowskie Centrum Rehabilitacji i Ortopedii | Krakow | Malopolska |
Lead Sponsor | Collaborator |
---|---|
Jagiellonian University |
Poland,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Oswestry scale | Oswestry Disability Index (ODI) can be used for evaluation both cervical and lumbar spine. It is the most common method used for disability evaluation of patients with neck pain. It consits of questiones which evaluate how the pain limits activities. There are 10 questiones concerning ADLs. | Change from baseline Oswesstry scale at 2 weeks. | |
Secondary | VAS scale | One of the most commonly used scale for pain evaluation is Visual Analogue Scale (VAS). It is easy to use, it doesn`t require any verbal or reading abilities and it`s comprehensive enough. A patient is asked to indicate his/her perceived pain intensity (most commonly) along a 100 mm horizontal line, and this rating is then measured from the left side. | baseline, two weeks, 3 months | |
Secondary | assessment of the occurrence of vertigo, balance problems,nausea,limited ROM in shoulder joints | There were closed questiones with yes or no answer | baseline, two weeks, 3 months | |
Secondary | ROM evaluation | ROM of cervical spine was evaluated with a measuring tape | baseline, two weeks, 3 months |