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Effects of a randomized trial of resistance dynamic stabilization training on Fitness and Quality of Life in the management of chronic nonspecific low-back pain

A randomised controlled trial on the effects of resistance dynamic stabilization training on Fitness and Quality of Life in the management of chronic nonspecific low-back pain

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12614000818639
Enrollment
30
Registered
2014-07-31
Start date
2013-02-25
Completion date
2013-06-03
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

We tested the hypothesis that resistance dynamic stabilization training increases the physical fitness and HRQOL and decreases the levels of pain and disability in patients with CLBP.

Interventions

Subjects were cited in the laboratory 2 weeks before starting the experimental protocol and performed 2 sessions of 2 hours, to collect personal and familiarization with the exercises information. The exercise group (EG) exercised in Physiotherapy Clinic, two times per week for a 12-week period. EG was monitored by the same specialist (qualified personnel), who led each training session. At least one trained monitor was always present to verify the correct application of the methodology. Each t

Subjects were cited in the laboratory 2 weeks before starting the experimental protocol and performed 2 sessions of 2 hours, to collect personal and familiarization with the exercises information. The exercise group (EG) exercised in Physiotherapy Clinic, two times per week for a 12-week period. EG was monitored by the same specialist (qualified personnel), who led each training session. At least one trained monitor was always present to verify the correct application of the methodology. Each therapy session ranged from 45 to 60 min depending on the phase. A warm-up of 6-7 min of mild cardiovascular exercise followed by 3-4 min of stretching was always performed prior to the training sessions. A cool-down of 1 min of mild cardiovascular exercise followed by 4 min of stretching was always performed after the training sessions. The subjects were instructed in the different exercise techniques and in controlling exercise intensity through the combined use of a targeted number of repetitions and perception of effort during two sessions before beginning the training program. The criteria of body position, ranges of motion and movement speed described. The load (resistance) for each exercise was determined according to the rating of perceived exertion in active muscles by using the OMNI resistance exercise scale for active muscles. The control of neutral lordosis for seat pull and row exercises was determined with the pressure changes on biofeedback meter.

Sponsors

University of Alicante
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Educational / counselling / training
Masking
Blinded (masking used) (Investigator)

Eligibility

Sex/Gender
All
Age
20 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

*women between 20 and 55 years of age; *subjects had low back pain as a primary complaint, without associated leg pain; *all subjects suffered from chronic (>3 months, >3 d·wk-1) nonspecific (soft tissue in origin) low-back (lumbar 5 to lumbar 1) pain; and *no history of formal exercise training

Exclusion criteria

*were receiving concurrent treatments from another practitioner for their low back pain; *were diagnosed as having a tumor, infection, or inflammatory disease affecting the spine; *had spinal or lower-limb surgery; *had spinal fractures or structural deformities such as spondylolisthesis and spondylolysis; *had any contraindications to exercise therapy (e.g., uncontrolled hypertension, previous myocardial infarction, cerebrovascular disease, peripheral vascular disease, respiratory disorders); *were involved in workers’ compensation claims; *had signs of nerve root compromise, defined as decreased tendon reflexes, sensory loss, and motor deficits; and *were receiving medications other than analgesics and nonsteroidal anti-inflammatory drugs.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026