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Comparison of Different Manual Therapy Approaches in Patients With Chronic Neck Pain

Not Applicable
Not yet recruiting
Conditions
Neck Pain
Interventions
Other: Massage group
Other: Connective tissue massage group
Other: Mobilization group
Registration Number
NCT05769179
Lead Sponsor
Ankara Yildirim Beyazıt University
Brief Summary

The aim of the study was to compare the effects of different manual therapy approaches on pain, cervical range of motion, balance, functional status and life quality in patients with chronic neck pain.

Detailed Description

Various physiotherapy and rehabilitation methods are applied in the treatment of patients with chronic neck pain. Clinical practice guidelines for individuals with chronic neck pain recommend both manual therapy and exercise therapy among conservative treatments. Manual therapy are methods that can be safely applied to soft tissues and joints. Both manual therapy and exercise applications have been shown to have positive effects on neck pain and function. Some studies in the literature have also shown that manual therapy methods have positive effects on balance. However, no study examining the effects of different manual therapy (classical massage, connective tissue massage, manual joint techniques) approaches applied to individuals with chronic neck pain on pain, cervical range of motion, balance, functional status and quality of life was found in the literature.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  • To be between the ages of 18-65.
  • To participate in the study voluntarily.
  • Having a complaint of neck pain for at least 3 months.
Exclusion Criteria
  • To have undergone cervical spine surgery
  • Having cervical fracture and/or joint subluxation/dislocation
  • Severe degenerative arthritis
  • Having a neurological disease (Parkinson's disease, poliomyelitis, etc.) or an -inflammatory rheumatic disease (ankylosing spondylitis, rheumatoid arthritis, etc.)
  • Presence of malignancy
  • Having cord compression and signs
  • Severe radiculopathy or myelopathy
  • Positive vertebrobasilar artery test,
  • Pregnancy

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Massage groupMassage groupMassage group will be applied classic massage+cervical stabilisation exercises
Connective tissue massage groupConnective tissue massage groupConnective tissue group will be applied connective tissue massage+cervical stabilisation exercises
Mobilization groupMobilization groupMobilization group will be applied cervical mobilization techniques+cervical stabilisation exercises
Primary Outcome Measures
NameTimeMethod
Pain Intensitychange from baseline at 4 weeks

Pain intensity will be assessed with the Visual Analogue Scale (a 100 mm long horizontal line). Patient will be asked to score the pain he/she feels out of 10. The beginning of the figure is "0 "no pain", ending in "10 "there is unbearable pain".

Secondary Outcome Measures
NameTimeMethod
Pressure Pain Thresholdchange from baseline at 4 weeks

Pressure Pain Threshold will be assessed with a digital algometer device. The device that objectively measures the pain threshold will be used for the evaluation. The probe of the device will be pressed on the trapezius muscle. The first pain threshold felt will be recorded.

Cervical Range of Motionchange from baseline at 4 weeks

Cervical range of motion will be evaluated with a goniometer in the sitting position. Neck flexion, extension, right-left lateral flexion and right-left rotation ranges of motion will be recorded

Balancechange from baseline at 4 weeks

Balance will be evaluated with the Biodex Balance System Device. The individual is placed on a platform of the device that evaluates the ability to keep the centre of gravity on the support surface. Changes in the centre of gravity of the individual standing on this platform will be recorded with this device in static and dynamic, with eyes open and closed.

Functional Statuschange from baseline at 4 weeks

Functional Status will be assessed with Neck Disability Index. This index consists of 10 items. Each item was scored from 0 (no disability) to 5 (complete disability). The total score ranged from 0 (no disability) to 50 (total disability). As the score increased, disability increased and as the score decreased, disability decreased.

Life qualitychange from baseline at 4 weeks

Life quality will be assessed with Short Form-36 questionnaire. The questionnaire consists of 36 items. Scoring is done over 100 points and the scores are between 0 and 100 points for each sub-parameter. "0" is calculated as the worst value and "100" as the best value.

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