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Clinical Trials/NCT05680493
NCT05680493
Active, not recruiting
Not Applicable

Comparison of Dry Needling and Manual Pressure Release for Managing Low Back Pain

Foundation University Islamabad1 site in 1 country30 target enrollmentOctober 1, 2022
ConditionsLow Back Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Low Back Pain
Sponsor
Foundation University Islamabad
Enrollment
30
Locations
1
Primary Endpoint
pain intensity
Status
Active, not recruiting
Last Updated
3 years ago

Overview

Brief Summary

This study will compare the effect of dry needling and manual pressure in patients having low back pain in terms of pain and disability. There will be two groups ; experimental and control. Half of study group will receive dry needling session along with hot pack. Half of study group will receive manual pressure technique along with hot pack.

Detailed Description

The study is Randomized Control Trail , which is being conducted in fauji foundation hospital and Foundation University College Of Rehabilitation (oct 2022-feb 2023) . Sample size of 50 individual was calculated using epitool with 95% confidence interval (CI), and power 80%. sample will be collected through pilot study . both groups will recieve conventional physiotherapy protocol (hot pack) Assessment will be done on baseline, and 4th week .

Registry
clinicaltrials.gov
Start Date
October 1, 2022
End Date
February 1, 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • age between 30-60
  • pateint with subacute and chronic low back pain at least last 6 months.
  • pateint with active MTrps.

Exclusion Criteria

  • patient with fibromyalgia
  • pregnant females
  • patient with chronic diseases (osteoporosis, lungs disease and diabetes)
  • patient with musculoskeletal injuries
  • patient that are using any medication to relief pain like analgesic or muscle relaxants
  • Any treatment for back pain in same period of research.
  • patient having any radiculopathies or discogenic low back pain

Outcomes

Primary Outcomes

pain intensity

Time Frame: 4 weeks

visual analogue scale

functional disability

Time Frame: 4 weeks

functional disability will be measured through oswestry disability index

Study Sites (1)

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