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combined Pilates exercises

Comparison of the effect of two combined Pilates protocols on the level of pain, balance, range of motion and proprioception in young people with non-specific chronic low back pain

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250920067295N1
Enrollment
30
Registered
2026-02-14
Start date
2026-02-18
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Chronic non-specific low back pain.

Interventions

Intervention 1: Intervention group: pilates with walking. Intervention 2: Intervention group: Pilates with stretching exercises.

Sponsors

the university of shahid beheshti
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 30 Years

Inclusion criteria

Inclusion criteria: No respiratory problems Age between 20 and 30 years Normal body mass index (19 to 25) No pathological problems, spinal stenosis, or herniated discs Pain due to muscle weakness History of back pain for more than three months No abnormalities in the spine and lower extremities No history of surgery in the spine and lower extremities Self-reported pain 4 to 6 VAS index

Exclusion criteria

Exclusion criteria: Feeling pain and disability during the training period Absence from more than 2 sessions of the entire training program Unwillingness of the subject to continue the research Not participating in training sessions regularly

Design outcomes

Primary

MeasureTime frame
Plyometric Combination Protocol. Timepoint: Before the intervention, 8 weeks after the intervention. Method of measurement: VAS index questionnaire for pain assessment, stork test for static balance, Y test for dynamic balance, tape measure for lumbar range of motion, goniometer for pelvic proprioception.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFateme azimi behmand

The university of Shahid beheshti

fatemeazimibehmand5193@gmail.com+98 81 3251 5205

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026