Combined and Aquatic Exercise in Chronic Low Back Pain
Starting soon · Not applicable
Conditions studied: Chronic Low-back Pain (cLBP)
In brief
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.
Key facts
- Study ID
- NCT07732595
- Run by
- University of Beira Interior
- People needed
- 90
- Starts
- 2026-09-01
- Expected to finish
- 2027-05-01
- Last updated by the study team
- 2026-07-30
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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.
You may not qualify if…
- 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.
Where it is running
- University of Beira Interior — Covilha, Castelo Branco District, Portugal
Full record on ClinicalTrials.gov
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