The Association Between Amputation Level and Chronic Low Back Pain After Combat-Related Amputation (LEVEL-BACK)
Patients with combat-related lower limb amputations frequently experience chronic low back pain during long-term rehabilitation and prosthetic use. Altered biomechanics, asymmetric loading, gait disturbances, and changes in spinal alignment after limb loss may contribute to the development of persistent back pain. The severity and characteristics of low back pain may vary according to the level of amputation.
The LEVEL-BACK Study is a prospective observational study designed to evaluate the relationship between amputation level and chronic low back pain after combat-related amputation.
Participants with different levels of lower limb amputation will undergo clinical assessment of low back pain intensity, functional limitations, prosthesis use, and rehabilitation outcomes during follow-up.
The goal of the study is to improve understanding of how amputation level influences chronic low back pain after combat-related limb loss and to identify patients at increased risk for persistent spinal pain during rehabilitation.
研究概览
详细说明
Chronic low back pain is a common long-term complication following lower limb amputation and may significantly impair mobility, rehabilitation, prosthesis tolerance, and quality of life. Patients with combat-related amputations are particularly vulnerable because of severe tissue trauma, altered gait mechanics, asymmetric loading, repeated surgical interventions, and prolonged rehabilitation.
Biomechanical alterations after amputation may lead to abnormal spinal loading, pelvic asymmetry, trunk compensation, and increased energy expenditure during ambulation. These changes may contribute to chronic mechanical stress on the lumbar spine and development of persistent low back pain. The level of amputation may play an important role in this process, as more proximal amputations are frequently associated with greater gait disturbance, increased compensatory trunk movements, and higher biomechanical demand during prosthetic walking.
Despite increasing recognition of chronic low back pain after amputation, limited prospective data are available regarding the relationship between amputation level and spinal pain severity in combat-related trauma populations.
The LEVEL-BACK Study is a prospective observational study designed to evaluate the association between lower limb amputation level and chronic low back pain after combat-related amputation.
Participants with transtibial, transfemoral, and bilateral lower limb amputations will undergo longitudinal clinical assessment during rehabilitation follow-up. Study evaluations will include assessment of low back pain intensity, duration of symptoms, prosthesis use, functional mobility, rehabilitation outcomes, and pain-related disability.
The study aims to improve understanding of spinal pain mechanisms after combat-related limb loss and identify patient groups at increased risk for chronic low back pain according to amputation level.
研究类型
注册 (估计的)
联系人和位置
学习联系方式
- 姓名:Dmytro Dmytriiev, PhD.Professor
- 电话号码:+380674309449
- 邮箱:mddmytriiev@gmail.com
学习地点
-
-
-
Vinnytsia、乌克兰、21000
- Vinnitsya university hospital
-
接触:
- Dmytro Dmytriiev, Phd
- 电话号码:0674309449
- 邮箱:mddmytriiev@gmail.com
-
-
参与标准
资格标准
适合学习的年龄
- 成人
接受健康志愿者
取样方法
研究人群
描述
Inclusion Criteria:
- Age ≥18 years
- Combat-related lower limb amputation
- Transtibial, transfemoral, or bilateral lower limb amputation
- Time since amputation ≥3 months
- Current or planned prosthesis use
- Ability to participate in rehabilitation assessment
- Ability to report low back pain intensity
- Ability to provide written informed consent
Exclusion Criteria:
- Traumatic spinal injury related to the initial combat trauma
- Previous spinal surgery before amputation
- Known severe spinal deformity
- Active spinal infection or malignancy
- Severe neurological disorder affecting mobility
- Non-combat-related amputation
- Inability to complete follow-up assessments
- Refusal or inability to provide informed consent
学习计划
研究是如何设计的?
设计细节
队列和干预
团体/队列 |
|---|
|
Transtibial Amputation
Participants with unilateral transtibial (below-knee) combat-related lower limb amputation.
|
|
Transfemoral Amputation
Participants with unilateral transfemoral (above-knee) combat-related lower limb amputation
|
|
Bilateral Lower Limb Amputation
Participants with bilateral combat-related lower limb amputation.
|
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 |
|---|---|---|
|
Change in chronic low back pain intensity
大体时间:Baseline to 12 months
|
Assessment of change in low back pain intensity using the Numeric Rating Scale, where 0 indicates no pain and 10 indicates the worst imaginable pain.
|
Baseline to 12 months
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Low Back Pain Disability Assessed Using the Oswestry Disability Index (ODI)
大体时间:Baseline, 3 months, 6 months, and 12 months after amputation.
|
Low back pain-related disability will be assessed using the Oswestry Disability Index (ODI), a validated questionnaire designed to evaluate functional impairment associated with low back pain. The ODI consists of 10 sections covering pain intensity and activities of daily living. Total scores range from 0 to 100, with higher scores indicating greater disability and worse functional status. Scale Information: Oswestry Disability Index (ODI) Minimum Value: 0 Maximum Value: 100 Interpretation: Higher scores indicate greater low back pain-related disability and worse functional outcomes. |
Baseline, 3 months, 6 months, and 12 months after amputation.
|
|
Low Back Pain Disability Assessed Using the Roland-Morris Disability Questionnaire (RMDQ)
大体时间:Baseline, 3 months, 6 months, and 12 months after amputation.
|
Low back pain-related disability will be assessed using the Roland-Morris Disability Questionnaire (RMDQ), a validated 24-item patient-reported outcome measure designed to evaluate functional limitations associated with low back pain. Participants indicate whether each statement applies to them on the day of assessment. Total scores range from 0 to 24, with higher scores indicating greater disability and worse functional status. Scale Information: Roland-Morris Disability Questionnaire (RMDQ) Minimum Value: 0 Maximum Value: 24 Interpretation: Higher scores indicate greater disability related to low back pain and worse functional outcomes. |
Baseline, 3 months, 6 months, and 12 months after amputation.
|
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
关键字
其他研究编号
- 11v313022026
- USRA (其他标识符:Ukranian Society of Regional Anesthesia and Pain Therapy)
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
IPD 共享支持信息类型
- 研究方案
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.