Skip to content

Plus Deep Water Running on Low Back Pain

Evidence-Based Physiotherapy With and Without Deep Water Running on Non-Specific Low Back Pain. A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00888524
Acronym
+DWR
Enrollment
46
Registered
2009-04-27
Start date
2006-01-31
Completion date
2007-09-30
Last updated
2009-04-27

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

Conditions

Low Back Pain

Keywords

head out water immersion,, high intensity exercise,, evidence-based physiotherapy;, aquatics;, hydrotherapy, aquatics therapy, exercise therapy

Brief summary

Objectives: To evaluate the effect size on non-specific chronic low back pain (CLBP) of evidence-based physiotherapy (EBP) with and without the addition of deep water running (DWR) on pain, physical disability and general health state. Materials and methods: Randomized, double-blind, controlled trial (therapists and assessors) involving 46 persons with CLBP over 15 weeks with two interventions, presented three times a week. Each group received EBP (personalized exercise program, manual therapy and health education) while one group performed supplementary 20 min sessions of DWR at the individualized aerobic threshold. Measurements were made pre and post intervention for pain, disability and general health. Range of motion of lumbar spine in the sagittal plane, maximum isometric strength and muscle endurance of lumbar and hip extensors was assessment.

Interventions

PROCEDUREGP in Physio

manual therapy, educational advice of health promotion and physical exercises therapy based in a individual assessment

PROCEDUREGP in Physio plus DWR

GP in Physio plus a supplementation of DWR training in high intensive aerobic threshold

Sponsors

University of Malaga
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Participants were diagnosed with non-specific CLBP, with no radiation to the legs, and lasting at least three months

Exclusion criteria

* Low back pain as a result of specific spinal disease, infection, tumor, osteoporosis, fracture, structural deformity, inflammatory disorder, radicular syndrome or caudal equine syndrome * Patients not able to follow instructions * Patients with any digressive condition

Design outcomes

Primary

MeasureTime frame
pain in VASscale 0 -100, pre and post intervention and follow up 6 and 12 month

Secondary

MeasureTime frame
disability RMQscale 0-24, pre and post intervention and follow up 6 and 12 month
general (mental and physical) health state with SF-12scale 0 -100, pre and post intervention and follow up 6 and 12 month
functional Measurements: range on motion in degrees with inclinometer dual, strength with lineal dynamometer (newton) and endurance muscular with soerensen test (seconds)scale physica of degrees, newtons and seconds pre post intervention and 6 and 12 month of follow up

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026