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Clinical Trials/CTRI/2022/10/046841
CTRI/2022/10/046841
Recruiting
未知

Effect of Home Exercise Programme on Pain, Functional Abilities and Quality of Life among adults with Chronic Non-specific Low Back Pain in rural areas.

Tamizh Maran0 sites0 target enrollmentTBD
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Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Tamizh Maran
Status
Recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Tamizh Maran

Eligibility Criteria

Inclusion Criteria

  • •1\. Male and female adults, aged between 25 and 55 years, residing in rural areas with persistent low back pain for about 12 weeks and less than 1 year duration.
  • •2\. Back Pain localised anywhere between the costal margin and the gluteal folds with no radiating pain, and able to perform the Activities of Daily Living (ADL) and occupational activities with the pain. (NPRS of score between 4 and 7, moderate level)
  • •3\. Positive outcome of balance by the Forward \& Lateral Reach Test among the study population.

Exclusion Criteria

  • •1\. ‘Red Flag’ symptoms including, a history of major trauma/ potential spinal fracture, inflammatory disease, infection, malignancy, persistent night pain, bladder or bowel dysfunction, and/or lower extremity neurological deficit.
  • •2\. Previous history of surgery to the lumbar spine, abdomen, pelvis, or hip
  • •3\. Congenital malformations like Severe spinal stenosis, cauda equina syndrome.
  • •4\. Acquired ailments like spondylolisthesis, spinal nerve root compression, Sacro\-iliac pathology, fibromyalgia
  • •5\. Therapeutic radiological interventions or injections in the past 3 months
  • •6\. Any contraindication for exercise therapy (e.g. uncontrolled hypertension, previous myocardial infarction, cardiovascular disease, peripheral vascular disease, respiratory disorders)
  • •7\. Study participants unable to perform isometric contraction and hold it for 30 seconds while testing
  • •8\. Pregnancy
  • •9\. Non\-consenting individuals

Outcomes

Primary Outcomes

Not specified

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