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Effectiveness of Pilates exercises in the treatment of chronic low back pain

Effectiveness of Pilates method in the treatment of nonspecific chronic low back pain: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-5w39snn
Enrollment
Unknown
Registered
2021-06-08
Start date
2015-03-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Individuals with chronic non-specific low back pain

Interventions

Pilates Group: 43 individuals with chronic non-specific low back pain. Each participant received 16 sessions of Pilates Method exercises. The program included floor and apparatus exercises (Barrel, Ca
in which information and recommendations related to posture, daily activities, information about lower back pain, spinal anatomy, and suggested exercises were explained. At the end of the meetings, ea

Sponsors

Pontifícia Universidade Católica de Minas Gerais
Lead Sponsor
Pontifícia Universidade Católica de Minas Gerais
Collaborator

Eligibility

Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Individuals aged between 18 and 60 years who had NSCLBP lasting for more than 3 months.

Exclusion criteria

Exclusion criteria: Autoimmune rheumatic and inflammatory diseases, lower extremity radiating pain, fibromyalgia, thyroid disease, pregnancy, neurological or cognitive diseases, morbid obesity, lower limb amputees, patients with uncontrolled disease (e.g. hypertension or heart disease)

Design outcomes

Primary

MeasureTime frame
Pain intensity: numerical rating scale (0 to 10), assessed at baseline, at the end of treatment and 2 months after treatment.;Quality of life: SF-36 questionnaire, assessed at baseline, at the end of treatment and 2 months after treatment.;Functional disability: using the Roland-Morris Disability Questionnaire (RMDQ), assessed at baseline, at the end of treatment and 2 months after treatment.

Secondary

MeasureTime frame
Flexibility: using the 3rd fingertip-to-floor test, assessed at baseline, at the end of treatment and 2 months after treatment.;Sleep Quality: the Pittsburgh Sleep Quality Index (PSQI), assessed at baseline, at the end of treatment and 2 months after treatment.

Countries

Brazil

Contacts

Public ContactEliane Machado
elianem_machado@hotmail.com+55-035-997412372

Outcome results

None listed

Source: REBEC (via WHO ICTRP)