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Low Back Pain and Hamstring-to-Quadriceps Strength Ratio in Military Personnel (LBP-H/Q ratio)

2026年5月18日 更新者:Vilma Dudoniene、Lithuanian Sports University

Association Between Low Back Pain and Hamstring-to-Quadriceps Strength Ratio in Lithuanian National Defence Volunteer Forces Personnel

The aim of this study was to determine the association between low back pain and the strength of knee flexor and extensor muscles in Lithuanian National Defence Volunteer Forces personnel.

研究概览

地位

完全的

详细说明

This cross-sectional study investigated the association between low back pain (LBP) and the hamstring-to-quadriceps (H/Q) strength ratio in personnel of the Lithuanian National Defence Volunteer Forces. Active-duty volunteers with and without LBP underwent isokinetic testing of knee flexor and extensor muscle strength using a Biodex System 4 Pro dynamometer at angular velocities of 60°/s and 120°/s. Hamstring strength, quadriceps strength, H/Q ratios, and inter-limb asymmetries were assessed to explore potential associations with low back pain in this military population.

研究类型

观察性的

注册 (实际的)

71

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • LT
      • Kaunas、LT、立陶宛、44221
        • Department of health promotion and rehabilitation

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 孩子
  • 成人
  • 年长者

接受健康志愿者

是的

取样方法

非概率样本

研究人群

The study population included active-duty Lithuanian National Defence Volunteer Forces personnel recruited for participation in this cross-sectional analysis

描述

Inclusion Criteria:

  • The study participants consisted of a targeted population of Lithuanian National Defence Volunteer Forces personnel

Exclusion Criteria:

  • Individuals with a clinically diagnosed low back pain disorder or acute episodes of low back pain were excluded

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
Military personnel
Targeted population of Lithuanian National Defence Volunteer Forces personnel

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
Low back pain prevalence
大体时间:Baseline
Participants were asked whether they had experienced low back pain during the past 12 months (yes/no). Participants who responded "yes" were classified into the low back pain group.
Baseline
Low back pain intensity
大体时间:Baseline
LBP intensity was assessed using the Visual Analogue Scale (VAS, 0-10) , where 0 - no pain, and 10 - worst imaginable pain.
Baseline
Low back pain duration
大体时间:Baseline
Participants were asked to indicate LBP duration. LBP pain duration was classified as acute (<3 months) or chronic (≥3 months)
Baseline
Muscle strength peak torque
大体时间:Baseline

Muscle strength was assessed using the Biodex System 4 isokinetic dynamometer. Participants were instructed to avoid vigorous physical activity 24 hours before testing and refrain from eating for at least 2 hours prior to assessment. A 10-minute warm-up on a cycle ergometer (50-60 W) and light dynamic exercises were performed before testing. Participants were seated with the backrest at 85° and hip flexion at 90°. The dynamometer axis was aligned with the lateral femoral epicondyle, and the lower leg was secured 2-3 cm above the ankle. The range of motion was set from 70° knee flexion to full extension. The trunk and tested limb were stabilized using straps.

Testing included 5 repetitions at 60°/s and 10 repetitions at 120°/s, with a 30-second rest interval between sets. Prior to testing, participants performed 3-5 familiarization repetitions.

Peak torque normalized to body weight (Nm/kg) was recorded.

Baseline
Average torque
大体时间:Baseline
Was measured in Nm
Baseline
Muscle power
大体时间:Baseline
in W
Baseline
Body weight
大体时间:Baseline
Measured in kg
Baseline
Body height
大体时间:Baseline
Measured in meters
Baseline
Age
大体时间:Baseline
Measured in years
Baseline

次要结果测量

结果测量
措施说明
大体时间
Previous injuries
大体时间:Baseline
Participants were asked whether they had lumbar or lower limb injuries during the past 12 months that could influence the results (yes / no).
Baseline

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年1月1日

初级完成 (实际的)

2026年1月5日

研究完成 (实际的)

2026年4月22日

研究注册日期

首次提交

2026年4月24日

首先提交符合 QC 标准的

2026年5月18日

首次发布 (实际的)

2026年5月26日

研究记录更新

最后更新发布 (实际的)

2026年5月26日

上次提交的符合 QC 标准的更新

2026年5月18日

最后验证

2026年1月1日

更多信息

与本研究相关的术语

其他研究编号

  • Lithuanian Sports University31

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

IPD 计划说明

Individual participant data (IPD) will not be publicly shared due to ethical and privacy restrictions related to participant confidentiality and informed consent agreements.Military personnel is sensitive

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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