Effects of Whole-Body Vibration and Cervical Stabilization With Core Stabilization in Young Adults With Non-Specific Low Back Pain
Effects of Whole-Body Vibration and Cervical Stabilization Combined With Core Stabilization on Trunk Motor Control in Young Individuals With Non-Specific Low Back Pain
This study aims to investigate the immediate effects of three intervention approaches in young adults with nonspecific low back pain. Participants will be randomly assigned to one of three groups: core stabilization exercises, whole-body vibration combined with core stabilization exercises, or cervical stabilization combined with core stabilization exercises. Outcomes will be assessed before and immediately after the intervention. The study will evaluate trunk motor control, pain intensity, pressure pain threshold, trunk muscle endurance, and balance. The purpose is to compare the immediate effects of these approaches and determine whether adding whole-body vibration or cervical stabilization to core stabilization produces additional benefits.
研究概览
地位
条件
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Mariam Abualkas Abualkas, Pt
- 电话号码:+905345526603
- 邮箱:2433095031@stu.istinye.edu.tr
研究联系人备份
- 姓名:Çiçek Günday Asst. Prof., Asst. Prof.
- 电话号码:+905071888848
学习地点
-
-
Istanbul
-
Istanbul、Istanbul、土耳其(türkiye)
- Istinye University Physiotherapy and Rehabilitation Application and Research Center (ISUFIZYOTEM)
-
接触:
- Nurgül Elbaşı Elbaşı
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Age between 18 and 30 years.
- Low back pain intensity of at least 3/10 on the Numeric Rating Scale.
- Low back pain symptoms for at least 6 months.
- Ability to understand and follow verbal instructions.
- No major neurological deficit.
- No physiotherapy for low back pain within the previous 6 weeks.
Exclusion Criteria:
- Low back pain with a specific etiology identified by a physician.
- Neurological, vestibular, rheumatological, or serious musculoskeletal disorders affecting balance or motor control.
- Use of medications that may affect balance or have potential neurotoxic effects.
- Degenerative diseases.
- Indication for surgical intervention.
- History of fracture or surgery within the previous 2 years.
学习计划
研究是如何设计的?
设计细节
- 主要用途:支持治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
有源比较器:Core Stabilization
Participants in this group will perform the standard core stabilization exercise program, including the abdominal drawing-in maneuver, heel slide, single-leg march, single-leg extended heel tap, bridge, bridge pulse, dead bug, modified curl-up, and semi-plank. The total intervention duration is approximately 20 minutes. |
Participants perform a core stabilization exercise program including the abdominal drawing-in maneuver, heel slide, single-leg march, single-leg extended heel tap, bridge, bridge pulse, dead bug, modified curl-up, and semi-plank. The program is designed to activate and control the deep trunk stabilizing muscles. |
|
实验性的:Whole-Body Vibration + Core Stabilization
Participants in this group will receive 5 minutes of whole-body vibration before the core stabilization exercise program. The vibration platform will be set at 30 Hz with an amplitude of 2 mm, and participants will stand with the knees slightly flexed during the vibration. Immediately afterward, participants will perform the same core stabilization exercise program used in the core stabilization group. After completing the core stabilization exercises, an additional 5 minutes of whole-body vibration will be applied using the same parameters. The total intervention duration is approximately 30 minutes. |
Participants perform a core stabilization exercise program including the abdominal drawing-in maneuver, heel slide, single-leg march, single-leg extended heel tap, bridge, bridge pulse, dead bug, modified curl-up, and semi-plank. The program is designed to activate and control the deep trunk stabilizing muscles. Whole-body vibration will be applied using a vibration platform at a frequency of 30 Hz and an amplitude of 2 mm. Participants will stand on the platform with the knees slightly flexed for 5 minutes before the core stabilization exercise program and for an additional 5 minutes after the program. |
|
实验性的:Cervical Stabilization + Core Stabilization
Participants in this group will perform cervical stabilization exercises before the core stabilization exercise program. The cervical exercises will be performed in supine using a pressure biofeedback unit placed under the cervical spine. Participants will perform controlled craniocervical flexion, progressing the target pressure from 20 mmHg to 30 mmHg in 2 mmHg increments. The cervical stabilization exercises will be performed for approximately 5 minutes before the core stabilization program and repeated for an additional 5 minutes afterward. The total intervention duration is approximately 30 minutes. |
Participants perform a core stabilization exercise program including the abdominal drawing-in maneuver, heel slide, single-leg march, single-leg extended heel tap, bridge, bridge pulse, dead bug, modified curl-up, and semi-plank. The program is designed to activate and control the deep trunk stabilizing muscles. Participants will perform cervical stabilization exercises in the supine position using a pressure biofeedback unit placed under the cervical spine. Controlled craniocervical flexion will be performed with progressive target pressures from 20 mmHg to 30 mmHg in 2 mmHg increments. The exercises will be performed for approximately 5 minutes before the core stabilization program and repeated for an additional 5 minutes afterward. |
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Trunk motor control (supine), Pressure Biofeedback Unit
大体时间:Baseline and immediately after the single intervention session
|
Deep abdominal muscle activation and lumbopelvic stability assessed with a pressure biofeedback unit in crook lying during the abdominal drawing-in maneuver, starting at 40 mmHg. The score is the absolute deviation from 40 mmHg (best of three trials); smaller values indicate better motor control. |
Baseline and immediately after the single intervention session
|
|
Trunk motor control (prone; transversus abdominis activation), Pressure Biofeedback Unit
大体时间:Baseline and immediately after the single intervention session
|
Activation of the transversus abdominis assessed in prone lying with the pressure biofeedback unit placed under the abdomen and inflated to 70 mmHg. Participants draw the abdominal wall in without moving the spine or pelvis. The score is the pressure reduction from 70 mmHg held steadily (best of three trials); larger reductions indicate better activation. |
Baseline and immediately after the single intervention session
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Pain intensity, Numeric Pain Rating Scale (NPRS)
大体时间:Baseline and immediately after the single intervention session
|
Self-reported low back pain intensity rated from 0 (no pain) to 10 (worst imaginable pain). Lower scores indicate less pain. |
Baseline and immediately after the single intervention session
|
|
Pressure pain threshold, lumbar multifidus
大体时间:Baseline and immediately after the single intervention session
|
Pressure pain threshold in kg/cm² measured with a pressure algometer 2 cm lateral to the L4 spinous process. The mean of three measurements is used. Higher values indicate lower pain sensitivity. |
Baseline and immediately after the single intervention session
|
|
Pressure pain threshold, erector spinae
大体时间:Baseline and immediately after the single intervention session
|
Pressure pain threshold in kg/cm² measured with a pressure algometer 3 cm lateral to the L3 spinous process. The mean of three measurements is used. Higher values indicate lower pain sensitivity. |
Baseline and immediately after the single intervention session
|
|
Pressure pain threshold, thoracolumbar fascia
大体时间:Baseline and immediately after the single intervention session
|
Pressure pain threshold in kg/cm² measured with a pressure algometer 5 cm lateral to the L3 level. The mean of three measurements is used. Higher values indicate lower pain sensitivity. |
Baseline and immediately after the single intervention session
|
|
Y-Balance Test composite score, right leg
大体时间:Baseline and immediately after the single intervention session
|
Maximum reach in the anterior, posteromedial and posterolateral directions while standing on the right leg, normalized to right lower limb length and expressed as a composite score (%). Higher scores indicate better dynamic balance. |
Baseline and immediately after the single intervention session
|
|
Y-Balance Test composite score, left leg
大体时间:Baseline and immediately after the single intervention session
|
Maximum reach in the anterior, posteromedial and posterolateral directions while standing on the left leg, normalized to left lower limb length and expressed as a composite score (%). Higher scores indicate better dynamic balance. |
Baseline and immediately after the single intervention session
|
|
Trunk flexor endurance test
大体时间:Baseline and immediately after the single intervention session
|
Isometric holding time in seconds in the trunk flexor endurance test (McGill). Longer holding time indicates greater trunk flexor endurance. |
Baseline and immediately after the single intervention session
|
|
Prone plank test
大体时间:Baseline and immediately after the single intervention session
|
Isometric holding time in seconds in the prone plank position. Longer holding time indicates greater trunk muscle endurance. |
Baseline and immediately after the single intervention session
|
|
Right side bridge test
大体时间:Baseline and immediately after the single intervention session
|
Isometric holding time in seconds in the right side bridge test (McGill). Longer holding time indicates greater lateral trunk endurance. |
Baseline and immediately after the single intervention session
|
|
Left side bridge test
大体时间:Baseline and immediately after the single intervention session
|
Isometric holding time in seconds in the left side bridge test (McGill). Longer holding time indicates greater lateral trunk endurance. |
Baseline and immediately after the single intervention session
|
合作者和调查者
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- 2026/226
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
Individual participant data will not be shared in order to protect the privacy and confidentiality of the participants.
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.