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Effectiveness of aquatic therapy versus standard physiotherapy in reducing pain in patients with chronic low back pain

Effectiveness of aquatic therapy versus standard physiotherapy in reducing pain in patients with chronic low back pain

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260424008
Enrollment
36
Registered
2026-04-24
Start date
2025-10-20
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic low back pain Chronic low back pain

Interventions

Participants will attend a 30-minute session once per week for 10 weeks, using an aquatic treadmill system. This system is adjusted to match each patient&#039
s physical condition, optimizing therapeutic outcomes through controlled water temperature, pH, and chlorine levels, along with treadmill speed adjustments for safety and efficacy.,A structured 10-wee
Experimental Procedure/Surgery,Active Comparator Procedure/Surgery
Hydrotherapy Program,Standard Physical Therapy (PT)

Sponsors

Orthopaedics department, Faculty of Medicine Siriraj Hospital, Mahidol University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Adults aged 18 years or older 2. Diagnosed with chronic low back pain (CLBP) for at least 3 months. 3. Moderate to severe pain, defined as a Visual Analog Scale (VAS) score of 4 or more at baseline.

Exclusion criteria

Exclusion criteria: 1. Contraindication for hydrotherapy -Active bleeding or open wounds. -Significant bowel or bladder incontinence. -Acute inflammatory conditions (such as fracture, neurological trauma). -Significant cardiac or respiratory instability. -Any unstable medical condition. -Fever or infection. 2. Presence of red flags or serious spinal pathology 3. Patient who had a chlorine allergy 4. Patient who had underwent recent lumbar spinal surgery within 12 months 5. Pregnancy

Design outcomes

Primary

MeasureTime frame
Change in pain intensity 10 weeks Visual Analog Scale (VAS)

Secondary

MeasureTime frame
1. Quality of life 10 weeks EQ-5D-5L questionnaire,2. Functional disability 10 weeks ODI questionnaire

Countries

Thailand

Contacts

Public ContactCholavech Chavasiri

Faculty of Medicine Siriraj Hospital, Mahidol University

cholavech.cha@mahidol.ac.th024197964

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026