Actively Recruiting

Phase Not Applicable
Age: 20Weeks - 40Weeks
All Genders
ID06987175

Effects of Sedante Neo Therapy on Pain, Range of Motion and Quality of Life in Patients With Non Specific Low Back Pain

Led by Riphah International University · Updated on 2025-07-04

40

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of SADANTE neo therapy on pain, range of motion, and quality of life in patients with non-specific low back pain. This study aims to help physiotherapists develop better treatment plans by exploring a non-pharmacological therapy option that may offer pain management benefits with minimal side effects. Participants will be randomly assigned to one of two groups. One group will receive conventional exercises consisting of 20 minutes of exercises performed 20 times with 10 seconds hold each. The other group will receive SADANTE neo therapy using a SAN machine with suction cups applied to the lumbar paraspinal muscles for about 10 minutes daily, combined with the same conventional exercises, over a period of about 4 weeks. During the study, participants will be evaluated using the McGill Pain Questionnaire at the 4th week to assess pain. Additional assessments include the Oswestry Disability Index and Rand 36-item Health Survey to evaluate disability and overall health status. Researchers will monitor range of motion and quality of life measures to understand the therapy's impact. The total participation period is approximately 4 weeks.

CONDITIONS

Brief Title

Effects of Sedante Neo Therapy on Pain, Range of Motion and Quality of Life in Patients With Non Specific Low Back Pain.

Who Can Participate

Age: 20Weeks - 40Weeks
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age group of 20 years to 40 years
  • Both male and female participants
  • Having non-specific low back pain
  • Having SF-MPQ score of 1 or 2 (mild to moderate pain)
  • Having Oswestry Disability Index score between 5 and 24
  • Having SF-36 health survey score below 50
  • Having range of motion below normal
Not Eligible

You will not qualify if you...

  • Below 20 years or above 40 years of age
  • Cervical pain, knee pain, and other unrelated conditions excluded
  • Children excluded
  • Presence of red flags such as tuberculosis, carcinoma, or heart disease
  • Open sores
  • Psychiatric diseases such as depression or phobias
  • History of surgery in the lumbar region

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - About 4 weeks

Participants receive either Sadante neo therapy along with conventional exercises or conventional exercises only to improve pain, range of motion, and quality of life for low back pain.

Daily treatment sessions for about 4 weeks

Trial Site Locations

Total: 1 location

1

Arthritis and pain care clinic Lahore.

Lahore, Punjab Province, Pakistan, 54000

Actively Recruiting

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Research Team

I

imran amjad, Phd

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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