The Effect of Tendon Release Techniques in Patients With Cervical Disc Herniation
- Conditions
- Cervical Disc Herniation
- Interventions
- Device: Enhanced golgi tendon organ stimulation
- Registration Number
- NCT06526325
- Lead Sponsor
- Istanbul Arel University
- Brief Summary
The goal of this clinical trial is to investigate the effect of using enhanced golgi tendon organ stimulation on symptoms in patients with cervical disc herniation. The main question\[s\] it aims to answer are:
* Enhanced Golgi tendon organ stimulation is effective in reducing symptoms in patients with cervical disc herniation.
* Enhanced golgi tendon organ stimulation is not effective in reducing symptoms in patients with cervical disc herniation.
Participants will receive enhanced golgi tendon organ stimulation to the Sternocleidomastoideus, platysma, longus colli, longus capitis, scalene, rhomboid major \& minor, levator scapulae and trapezius muscles for 3 weeks, 2 sessions per week for 45 minutes.
- Detailed Description
Participants diagnosed with cervical disc herniation will be included. Participants will receive 6 sessions of 45 minutes each, 2 sessions per week for 3 weeks. Sternocleidomastoideus, platysma, longus colli, longus capitis, scalene muscles, rhomboid major \& minor, levator scapulae and trapezius muscles and tendons of these muscles will be applied.
Two separate applications are performed with the stimulator and the algometer. After increasing the blood flow in the area for 30 seconds with the vibration of the stimulator up to the point of attachment of the tendon, a pressure of 0.5 kilograms is applied at an angle of 90 degrees at 0.5 cm intervals from the origin to the insertion of the muscle in the area with an algometer made of special steel. The aim of this treatment is to stabilise the contraction and relaxation mechanism by stimulating the Golgi tendon organ and to eliminate pain by relieving spasms.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 51
- Being diagnosed with cervical disc herniation
- Volunteering for the research
- Chronic bone disease
- Have had surgery for a cervical disc herniation
- Have a structural abnormality
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Application of enhanced Golgi tendon organ stimulation to patients Enhanced golgi tendon organ stimulation The effect of golgi tendon organ stimulation on the symptoms will be examined after applying the improved golgi tendon organ stimulation to patients diagnosed with cervical disc herniation and having pain, limitation of movement, spasm and tenderness in the neck region.
- Primary Outcome Measures
Name Time Method Pain assessment with algometer baseline, immediately after the 6 weeks intervention The sternocleidomastoid, platysma, longus colli, longus capitis, scalene, rhomboid major and minor, levator scapulae and trapezius muscles and their tendons are compressed to 0.5 kg using an algometer. The patient's response is used to determine whether or not there is pain.
SF-36 (short form-36) baseline, immediately after the 6 weeks intervention The Short Form-36 (SF-36) is a self-assessment scale and analyses 8 dimensions of health including physical function, social function, role limitations (due to physical and emotional reasons), mental health, vitality (energy), pain and general perception of health with 36 items. In scoring the scale, each sub-dimension is given a score between 0 and 100 points, where 0 points indicate that the quality of life dimension is poor and 100 points indicate that it is good.
- Secondary Outcome Measures
Name Time Method assessment of joint range of motion baseline, immediately after the 6 weeks intervention Range of motion of the cervical spine will be assessed with a goniometer.
visual analogue scale (VAS) baseline, immediately after the 6 weeks intervention For pain intensity according to VAS, "no pain" is usually graded as 0 points and "worst imaginable pain" as 10 points (10 cm scale). The ranges for pain intensity are \<3 mild pain, 3-6 moderate pain, \>6 severe pain.
Spurling Test baseline, immediately after the 6 weeks intervention With the patient in an upright sitting position, the clinician flexes and laterally flexes the patient's head and applies cranial to caudal compression. The test is considered positive if there is pain, numbness and tingling. A positive spurling test indicates that there may be a problem such as a possible nerve root compression in this area. If the test is negative, it is said that nerve root compression is less likely.
Endurance Test baseline, immediately after the 6 weeks intervention The patient performs flexion, extension, right lateral flexion, left lateral flexion, right rotation and left rotation. Meanwhile, the clinician maintains the position by applying the same force in the opposite direction of movement. A stopwatch is used to time the onset of pain. The longer the time, the better the outcome. A shorter time indicates a poor clinical prognosis.
Trial Locations
- Locations (1)
AS Physiotherapy Services centre
🇹🇷Istanbul, Turkey