Comparison of two different exercise training programme on reducing pain and movement fear and to improve quality of life in patients with long term low back pai

Phase 3

• Conditions: Health Condition 1: M539- Dorsopathy, unspecified

• Registration Number: CTRI/2023/08/056228
• Lead Sponsor: KMCH Institute of Health Sciences and Research

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 August 2023

Recruitment & Eligibility

• Status: Open to Recruitment
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1. Patients with Low back pain for more than 3 months.

2. Low back pain patients with the NPRS Score: 4-8

3. Patients with Low back pain without any other specific pathology confirmed by the Orthopaedician by clinical examination or CT scan or MRI scan.

4. Low back pain patients with the age group â?? 35 to 50 years.

5. Both male and female patients.

6. Stable medical condition to allow participation in the intervention and testing protocol.

7. Patients with the ability to understand and follow the therapist instructions.

8. Low back pain patients in the geographic area - Coimbatore city.

Exclusion Criteria

1. Low Back Pain with specific pathology. (eg, infection, tumour, osteoporosis, lumbar spine fracture, structural or congenital deformity, in�ammatory disorder, radicular syndrome, or cauda equina syndrome)

2. Patients with the history of recent spinal surgery or other surgeries which interrupts the exercise training or worsens the patientâ??s condition.

3. Pregnant women.

4. Patients with Neurological problem or other musculo-skeletal conditions which interrupts the exercise training or worsens the patientâ??s condition.

5. Patients with metal implant.

6. Patients with rheumatoid disorders.

7. Patients with unstable cardiac conditions.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
PainTimepoint: Baseline- before commencing the treatment <br/ ><br>Post test- at the end of 4th week of treatment

Secondary Outcome Measures

Name	Time	Method
Kinesiophobia <br/ ><br>Timepoint: Baseline- before commencing the treatment <br/ ><br>Post test- at the end of 4th week of treatment;Quality of lifeTimepoint: Baseline- before commencing the treatment <br/ ><br>Post test- at the end of 4th week of treatment