此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Combined and Aquatic Exercise in Chronic Low Back Pain

2026年7月28日 更新者:Joana Catarina Carvalho Borges、University of Beira Interior

Effects of Combined-exercise and Aquatic-exercise on Pain, Disability and Functional Capacity in Patients With Chronic Low Back Pain

The goal of this randomized clinical trial is to evaluate the effects of a combined aquatic- and land-based exercise program, as well as an aquatic-exercise program, compared with a control group receiving home-based exercise, on pain, disability, and functional capacity in adults with CLBP. Secondary objectives include examining the effects on fear of movement, anxiety and depression, quadriceps and hand-grip strength, and lumbar mobility. The main question it aims to answer is: "Which type of exercise program is most effective at improving pain, disability, functional capacity, fear of movement, anxiety and depression, quadriceps and hand-grip strength, and lumbar mobility in adults with chronic low back pain?".

Participants will perform an aquatic-based exercise program (aquatic group), a combined aquatic and land-based exercise program (aquatic and land group), or a land-based exercise program (home group).

Researchers will compare groups to find any differences in pain, disability, functional capacity, kinesiophobia, anxiety and depression, quadriceps and hand-grip strength, and lumbar mobility.

研究概览

研究类型

介入性

注册 (估计的)

90

阶段

  • 不适用

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。

学习联系方式

学习地点

    • Castelo Branco District
      • Covilha、Castelo Branco District、葡萄牙、6201-001
        • University of Beira Interior
        • 接触:
        • 首席研究员:
          • Joana Borges, MSc
        • 首席研究员:
          • Henrique Neiva, PhD
        • 首席研究员:
          • Diogo Monteiro, PhD
        • 副研究员:
          • Fernanda M. Silva, PhD
        • 副研究员:
          • Tiago Pastilha, MSc
        • 首席研究员:
          • Pedro Duarte-Mendes, PhD

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

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  • all genders;
  • aged over 18 years;
  • Chronic Low Back Pain lasting three months or longer and with an intensity of 3 or higher on the Visual Analogue Scale at rest.

Exclusion Criteria:

  • Individuals who refuse to participate or do not provide informed consent;
  • Pain radiating to the lower limb;
  • Recent pregnancy or childbirth (less than 8 weeks ago);
  • Ongoing physical therapy treatments;
  • Severe rheumatological, neurological, neoplastic, cardiovascular diseases or other conditions that could prevent full participation in the intervention;
  • History of spinal surgery;
  • Inflammatory, infectious, or malignant spinal diseases;
  • Psychiatric disorders that may affect adherence and symptom assessment.

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

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
实验性的:Aquatic and Land Group
This arm will include 24 exercise sessions (three non-consecutive sessions per week), conducted over an 8-week period. 16 sessions of the aquatic-exercise program and 8 sessions of the land-based exercise program.

This intervention will consist of an aquatic-exercise program, performed in shallow water (120-150 cm deep) at a temperature of 32-34 °C, and supervised by a physiotherapist with over two years of experience in aquatic-based exercise and Ai Chi method.

The aquatic-exercise sessions, will consist of a 5-minute warm-up phase, a 30-40-minute training phase, and a 10-15-minute relaxation/cool-down phase, adapted from Ai Chi exercise positions. The Ai Chi method consists of 19 katas (movements) that incorporate deep breathing, coordinated upper and lower limb actions, trunk control, and slow, continuous motion. In this study, only 10 of these 19 katas will be included in the aquatic-exercise protocol.

This program will include specific land-based exercises, supervised by a physiotherapist with more than two years of experience in therapeutic exercise. The land-based exercise program, will be divided into three components: core stability exercises (15-20 minutes), trunk and lower limb stretching exercises (10-15 minutes), and relaxation/coordination exercises adapted from the Ai Chi method (10-15 minutes).
实验性的:Aquatic Group
This arm will comprise 24 sessions of the aquatic-exercise program (three non-consecutive sessions per week), conducted over an 8-week period.

This intervention will consist of an aquatic-exercise program, performed in shallow water (120-150 cm deep) at a temperature of 32-34 °C, and supervised by a physiotherapist with over two years of experience in aquatic-based exercise and Ai Chi method.

The aquatic-exercise sessions, will consist of a 5-minute warm-up phase, a 30-40-minute training phase, and a 10-15-minute relaxation/cool-down phase, adapted from Ai Chi exercise positions. The Ai Chi method consists of 19 katas (movements) that incorporate deep breathing, coordinated upper and lower limb actions, trunk control, and slow, continuous motion. In this study, only 10 of these 19 katas will be included in the aquatic-exercise protocol.

有源比较器:Home Group
This arm will include 24 sessions of the home-based exercise program (three non-consecutive sessions per week) over an 8-week period.
This exercise program will consist of a home-based exercise program. Each session will last 20-30 minutes and will be performed individually at home without professional supervision. The home-based exercise program will include core stability exercises that progress from the supine to the quadruped position. It will mirror the land-based exercise program and is adapted from a previous unsupervised home-based protocol.

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
Visual Analogue Scale
大体时间:One measurement will be assessed at baseline and one at each follow-up (8 and 12 weeks).
Pain intensity will be assessed with the Visual Analogue Scale (Minimum: 0; Maximum 10). Higher values correspond to worse outcome.
One measurement will be assessed at baseline and one at each follow-up (8 and 12 weeks).
Oswestry Disability Index - version 2.0
大体时间:One measurement will be assessed at baseline and one at each follow-up (8 and 12 weeks).
Disability due to low back pain will be assessed with the Oswestry Disability Index (Minimum: 0; Maximum 100). Higher values correspond to worse outcome.
One measurement will be assessed at baseline and one at each follow-up (8 and 12 weeks).
Short Physical Performance Battery
大体时间:One measurement will be assessed at baseline and one at each follow-up (8 and 12 weeks).
Lower-limb functional capacity (balance, gait speed, chair stands) will be assessed with the Short Physical Performance Battery, a simple tool that includes the four-meter gait speed test, the five-repetition sit-to-stand test and a balance test, and gives a total score based on the performance in each of those tests. Each component is scored (0-4), yielding a composite score (0-12), with higher scores indicating better performance.
One measurement will be assessed at baseline and one at each follow-up (8 and 12 weeks).

次要结果测量

结果测量
措施说明
大体时间
Tampa Scale of Kinesiophobia-13
大体时间:One measurement will be assessed at baseline and one at each follow-up (8 and 12 weeks).
Fear of movement will be assessed with the Tampa Scale of Kinesiophobia-13 (Minimum: 13; Maximum 52). Higher values correspond to worse outcome.
One measurement will be assessed at baseline and one at each follow-up (8 and 12 weeks).
Hospital Anxiety and Depression Scale
大体时间:One measurement will be assessed at baseline and one at each follow-up (8 and 12 weeks).
Anxiety and depression will be assessed with the Hospital Anxiety and Depression Scale (Minimum: 0; Maximum 21). Higher values correspond to worse outcome.
One measurement will be assessed at baseline and one at each follow-up (8 and 12 weeks).
Fixed Handheld Dynamometry for Assessing Quadriceps Strength
大体时间:Three measurements will be assessed at baseline and three at each follow-up (8 and 12 weeks).
Quadriceps muscle (both sides) maximum voluntary isometric contraction will be assessed with Fixed Handheld Dynamometry with participants seated and the knee positioned at approximately 90° of flexion.
Three measurements will be assessed at baseline and three at each follow-up (8 and 12 weeks).
Hand-Grip Dynamometry
大体时间:Three measurements will be assessed at baseline and three at each follow-up (8 and 12 weeks).
Maximum isometric strength of the hand and forearm muscles (both sides) will be assessed with Hand-Grip Dynamometry with participants seated with the elbow flexed at 90° and the forearm in a neutral position.
Three measurements will be assessed at baseline and three at each follow-up (8 and 12 weeks).
Modified-Modified Schober Test
大体时间:Three measurements will be assessed at baseline and three at each follow-up (8 and 12 weeks).
Lumbar spine range of motion will be assessed with the Modified-Modified Schober Test.
Three measurements will be assessed at baseline and three at each follow-up (8 and 12 weeks).

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。

调查人员

  • 研究主任:Diogo Monteiro, PhD、Instituto Politécnico de Leiria
  • 研究主任:Pedro Duarte-Mendes, PhD、Instituto Politécnico de Castelo Branco
  • 研究主任:Henrique Neiva, PhD、University of Beira Interior

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 (估计的)

2026年9月1日

初级完成 (估计的)

2027年2月1日

研究完成 (估计的)

2027年5月1日

研究注册日期

首次提交

2026年7月23日

首先提交符合 QC 标准的

2026年7月23日

首次发布 (实际的)

2026年7月29日

研究记录更新

最后更新发布 (实际的)

2026年7月30日

上次提交的符合 QC 标准的更新

2026年7月28日

最后验证

2026年7月1日

更多信息

与本研究相关的术语

其他研究编号

  • CE-UBI-Pj-2026-064

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

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

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.

订阅