Comparison of the Immediate Effects of Manual Therapy Techniques in Non-Specific Neck Pain
- Conditions
- Manual TherapiesNeck Pain
- Registration Number
- NCT06959160
- Lead Sponsor
- Halic University
- Brief Summary
The aim of this study is to investigate the effects of manual therapy techniques on joint range of motion, pain tolerance, grip strength, and functionality in individuals with non-specific neck pain. The study is experimental in design. Individuals aged between 18 and 55 who were diagnosed with non-specific neck pain and met the inclusion criteria participated in the study.
- Detailed Description
Participants who agreed to take part and signed the informed consent form were asked to complete the "Patient Assessment Form" during the initial interview.
In addition, the following assessment tools were used: the Cervical Range of Motion (CROM) device to evaluate joint range of motion, a hand dynamometer to assess grip strength, an algometer to measure pain tolerance, and the "Neck Disability Index" to evaluate functionality.
Participants were then randomly assigned to one of three groups:
Group 1: Atlanto-occipital manipulation
Group 2: Cervical mobilization
Group 3: Trigger point therapy
Participants in the first group received atlanto-occipital manipulation, those in the second group underwent Grade II-III mobilization techniques, and those in the third group received trigger point therapy, which consisted of ischemic compression followed by myofascial stretching on the upper trapezius muscle.
Immediately after the treatments, joint range of motion, pain tolerance, and functionality were reassessed. The manual therapy interventions for all three groups were performed by different specialized physiotherapists trained in these techniques. The evaluations, however, were conducted by another physiotherapist who was blinded to the treatments (double-blind study).
The data were statistically analyzed using the Statistical Package for the Social Sciences program, and a p-value of less than 0.05 was considered statistically significant.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 39
- Be between the ages of 18 and 55
- Have been diagnosed with non-specific neck pain by a specialized physician
- Have been experiencing neck pain for less than 3 months
- Have a neck pain level of at least 3 on the Visual Analog Scale
- Have bilateral active trigger points in the upper trapezius muscle
- Have restricted active cervical range of motion
- Presence of neurological deficit or radicular pain
- History of pathology or surgery in the cranio-cervical region
- Positive response in the extension-rotation test
- Use of anticoagulants or corticosteroids
- Presence of one or more red flags defined for non-specific neck pain
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Assessment of Cervical Joint Range of Motion Immediately before and after interventions, assessed within a single session The evaluation of cervical flexion, extension, right-left lateral flexion, and right-left rotation range of motion conducted using the CROM device. The CROM device is an inclinometer system affected by magnetic forces and gravity. Validity and reliability studies have been carried out to assess the movements of the cervical region using this device. There are no risks or side effects associated with this assessment method.
Assessment of Grip Strength Immediately before and after interventions, assessed within a single session Grip strength of the individuals was measured using the "Jamar Hand Dynamometer" (Takei Scientific Instruments Co., Ltd. - Japan). Measurements were conducted as recommended in the literature, with the patient comfortably seated, shoulder abducted, elbow in 90 degrees of flexion, forearm in a neutral position, and wrist in 0-30 degrees of extension. Measurements were repeated three times with five-second intervals between each trial for both the dominant and non-dominant hands, and the average value was recorded as the result. There are no risks or side effects associated with this assessment method.
Measurement of Pain Tolerance Threshold Immediately before and after interventions, assessed within a single session Pain tolerance was measured using the J-tech algometer device. Measurements were taken bilaterally, both on the right and left sides, at the C5 level and at the midpoint of the upper trapezius muscle. The measurements were repeated three times, and the average value was recorded as the result. There are no risks or side effects associated with this assessment method.
Neck Disability Index Immediately before and after interventions, assessed within a single session This questionnaire is used for the evaluation of cervical function and has undergone validity and reliability studies. The questionnaire consists of 10 sections, with 6 multiple-choice options for each section. Scoring ranges from 0 to 5 for each section based on the selected response. The total score determines the overall result of the test. There are no risks or side effects associated with this assessment method.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Halic University
🇹🇷Istanbul, Eyupsultan, Turkey
Halic University🇹🇷Istanbul, Eyupsultan, Turkey