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Effectiveness of Online Versus In-person Mat Pilates in Patients With Acute Non-Specific Low Back Pain

Comparison of Tele rehabilitation versus Conventional Mode of Mat Pilates in the Management of individuals with Acute Non-Specific Low Back Pain - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/086939
Enrollment
50
Registered
2025-05-14
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: M545- Low back pain

Interventions

Intervention1: Tele rehabilitation based Mat Pilates Program : The tele rehabilitation intervention consists of a structured mat Pilates exercise program specifically designed for individuals with acu

Sponsors

SRM College of Physiotherapy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Both male and female participants will be included. Participants aged between 20 years and 40 years will be included. Patients presenting with a Numerical Pain Rating Scale score of greater than or equal to 6 will be included. Individuals diagnosed with acute non-specific low back pain of less than 6 weeks duration will be included. Participants who are willing to take part in tele rehabilitation will be included. Patients currently undergoing conventional physiotherapy interventions will be included. Participants who have access to and are able to operate the necessary technology required for tele rehabilitation will be included.

Exclusion criteria

Exclusion criteria: Individuals with chronic pain syndromes will be excluded. Individuals who have undergone previous lumbar surgeries will be excluded. Patients diagnosed with lumbar pathologies such as spondylosis, spondylitis, or spondylolisthesis will be excluded. Patients currently undergoing alternative treatment protocols, for example ayurvedic and acupuncture will be excluded. Patients with co-morbidities such as cardiovascular, respiratory, or metabolic conditions will be excluded. Patients with chest and vertebral column deformities will be excluded. Patients with psychiatric disorders, including depression and schizophrenia, will be excluded. Pregnant women with low back pain symptoms will be excluded.

Design outcomes

Primary

MeasureTime frame
The Numerical Pain Rating Scale The Roland-Morris Disability Questionnaire The Patient Satisfaction Questionnaire 18Timepoint: The Numerical Pain Rating Scale - Baseline (Day 0) End of Intervention 1 (after 2 weeks of tele rehabilitation) End of Intervention 2 (after 2 weeks of conventional Pilates) The Roland-Morris Disability Questionnaire - Baseline (Day 0) End of Intervention 1 (after 2 weeks of tele rehabilitation) End of Intervention 2 (after 2 weeks of conventional Pilates) The Patient Satisfaction Questionnaire 18 - End of Intervention 1 (after 2 weeks of tele rehabilitation) End of Intervention 2 (after 2 weeks of conventional Pilates)

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactMr. Rajkumar M

SRM College of Physiotherapy

rajkumam2@srmist.edu.in7092022034

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026