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Lumbar and Gluteal Motor Control in Chronic Low Back Pain

Not yet recruitingNot applicableNCT07452172
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

The present study aims to evaluate the effectiveness of an 8-week combined lumbar motor control and gluteal muscle strengthening program in individuals with chronic non-specific low back pain

Study details

Official title
Efficacy of a Combined Lumbar Motor Control and Gluteal Strengthening Program on Pain and Function in Chronic Non-specific Low Back Pain
Conditions
Interventions
  • Device: Lumbar motor control exercises
  • Device: Gluteal strengthening exercises
Sponsor
University of Castilla-La Mancha
Start date
2026-03-02
Primary completion
2026-05-15
Sex
All
Age range
from 18 Years to 65 Years
Results posted
No results posted in this snapshot
Countries
Spain
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Age between 18 and 65 years. * Non-specific low back pain with an intensity greater than 3/10 on a visual analogue scale. * Symptom duration longer than 3 months. * Sufficient understanding of spoken and written Spanish to adequately comprehend the intervention instructions and complete the assessments. Exclusion Criteria: * Severe lumbar or hip trauma within the previous 6 weeks. * Prior vertebral fracture or lumbar disc herniation. * Fibromyalgia. * Active oncological disease. * Diagnosis of a severe psychiatric disorder. * Pregnancy. * Uncontrolled rheumatologic pathology. * Coexisting auto-immune pathology or chronic inflammatory disease.

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT07452172