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Lumbar Spine Rehab Application

Evaluation of efficacy of mobile application based data collection Vs conventional data collection for follow up of functional outcome following Interferential therapy and lower back strengthening exercises for lower back pathology using Oswestry Disability Index scoring system. - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/078165
Enrollment
30
Registered
2024-12-16
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: M498- Spondylopathy in diseases classified elsewhere

Interventions

Intervention1: NA: NA Control Intervention1: Evaluation of efficacy of mobile application based data collection Vs conventional data collection for follow up of functional outcome following Interferen

Sponsors

Dr Rajkumar Balasubramani
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Diagnosed with chronic lower back pain of more than 3 months. Currently undergoing interferential therapy and lower back strengthening exercises.

Exclusion criteria

Exclusion criteria: Severe neurological deficits. Recent spinal surgery (within the last 6 months). Other significant comorbidities affecting mobility or participation.

Design outcomes

Primary

MeasureTime frame
Improvement in Oswestry Disability Index (ODI) scores to assess functional outcomes following interferential therapy and lower back strengthening exercises.Timepoint: Baseline: Before starting the intervention. Midpoint: At 3 weeks into the intervention. Endpoint: At 6 weeks, upon completion of the intervention. Follow-up: At 12 weeks post-intervention to assess sustained outcomes.

Secondary

MeasureTime frame
Adherence to data collection methods, user satisfaction, and completeness of follow-up data using mobile applications versus conventional methods.Timepoint: Weekly: Throughout the 6-week intervention period for adherence and data completeness. Endpoint: At 6 weeks for overall user satisfaction and compliance. Follow-up: At 12 weeks post-intervention for sustained adherence and satisfaction.

Countries

India

Contacts

Public ContactDr Sanjay Raji

Saveetha Institute Of Medical And Technical Sciences, Saveetha Medical College And Hospitals

benjaminvinodh91@gmail.com9445711147

Outcome results

None listed

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