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Clinical Trials/NCT04815915
NCT04815915CompletedNot Applicable

Effects of Graston Technique in Patients With Non Specific Low Back Pain

Riphah International University2 sites in 1 country20 target enrollmentStarted: April 5, 2020Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
20
Locations
2
Primary Endpoint
PNRS

Study Overview

Brief Summary

Non-specific low back pain upsets individuals of all age gathering and is a most significant provider to illness load everywhere on the world. Overseeing rules prescribe emergency to locate the uncommon instances of low back pain that are brought about by actually genuine pathology, thus need demonstrative work-up or proficient arrangement, or both. Since non-specific low back pain doesn't have a known pathoanatomical cause and treatment accentuations on diminishing in agony and its meanings.

To determine the impacts of Graston technique in patients with non-specific low back pain.

This examination was Quasi Experimental study and on the basis of inclusion standards, 20 patients were involved. PNRS and ODI used to collect the data. Graston tool was used to treat patients 3 times in a week according protocol for 6 weeks' treatment plan with extensions bised exercises protocol following pattern of APTA. The data was analyzed using SPSS 21.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
20 Years to 40 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • • Both genders
  • Age (20-40 years)
  • Patients with non-specific backache
  • Trigger points and tender points at low back region

Exclusion Criteria

  • • Patients with chronic diseases
  • Degenerative changes in spine
  • Open wounds around the area to be treated
  • High blood pressure
  • Diabetic neuropathy
  • Cancer (depending on the type and location)
  • Taking anti-coagulants
  • Pregnancy

Outcomes

Primary Outcomes

PNRS

Time Frame: 2 months

Pain Numeric Rating Scale (PNRS) scores in subjects with moderate/severe pain at baseline. \*P \< 0.0001 vs. baseline. Includes only subjects with baseline PNRS score of 4 to 10. Scale ranges from 0 to 10. Data are shown as mean ± 95% confidence interval. n = 329 for all visits, all with a baseline PNRS score of 4 to 10.

OSWESTRY DISABILITY INDEX

Time Frame: 2 months

Each section is scored on a 0-5 scale, 5 representing the greatest disability. The index is calculated by dividing the summed score by the total possible score, which is then multiplied by 100 and expressed as a percentage. Thus, for every question not answered, the denominator is reduced by 5

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Maryam Shabbir

Associate Professor

Riphah International University

Study Sites (2)

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