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Effect of Strength Training for Chronic Low Back Pain Patients (IRMA20)

Effect of Strength Training for Chronic Low Back Pain Patients: Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03172962
Acronym
IRMA20
Enrollment
85
Registered
2017-06-01
Start date
2017-07-01
Completion date
2018-11-01
Last updated
2018-11-30

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

Conditions

Low Back Pain, Musculoskeletal Pain

Brief summary

Low back pain (LBP) is common in the population and has great socioeconomic consequences for societies across Europe and the United States. About a third of working-age adults have frequent LBP, and for about 10% the pain becomes chronic with consequences for work and leisure activities. A Cochrane review from April 2017 concluded that physical exercise is an intervention with few adverse events and positive outcomes on pain and function in adults with chronic pain. However, when scrutinizing the specific studies of the review there are large differences in adherence to the exercise interventions and consequently in the results obtained. Thus, there is a need for simple exercises that the patients can easily adhere to.

Interventions

BEHAVIORALStrength training

Specific strength training exercises for the lumbar and abdominal muscles for 8 weeks

Will receive the usual care at the hospital

Sponsors

National Research Centre for the Working Environment, Denmark
Lead SponsorOTHER_GOV
University of Valencia
CollaboratorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Non-specific Chronic low back pain patient (more than 3 months) at the hospital Arnau de Vilanova

Exclusion criteria

* Spine surgery * neurologic or psyquiatric disorders * Low back traumastism * Recent participation in a similar training program

Design outcomes

Primary

MeasureTime frameDescription
Low back pain intensitychange from baseline to 8-week follow-upLow back pain intensity (VAS 0-10)
Back pain recurrence1 to 100 days, beginning from the last day of termination of the 8-week interventionnumber of episodes with back pain recurrence after termination of the intervention

Secondary

MeasureTime frameDescription
Use of analgesicschange from baseline to 8-week follow-upNumber of days using analgesic within the last week
Roland-Morris disabilitychange from baseline to 8-week follow-upThe Roland-Morris disability questionnaire
Pain siteschange from baseline to 8-week follow-upNumber of pain sites
Handgrip strengthchange from baseline to 8-week follow-upMaximal force (kg) in handgrip
Muscle endurancechange from baseline to 8-week follow-upThe Biering-Sørensen test

Countries

Spain

Outcome results

None listed

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