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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-40
SponsorRiphah International University

About this trial

this study is to evaluate the effects of SADANTE neo therapy on pain, range of motion and quality of life in patients with non-specific low back pain.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age group of 20 yeras to 40 years.

Both male and female included.

Having non-specific low back pain.

Having SF-MPQ score 1and 2 (1 means mild, 2 means moderate)

Disqualifiers

Below 20 years and above 40 years patient are excluded

Cervical, knee pain and other conditions excluded.

Children are excluded

Red flags ( tuberculosis, carcinoma heart disease etc) excluded

Trial design

Design model

Parallel

Treatments tested in this trial

  • sadante neo therapy

    Other intervention

    SAN machine having 3 tube cords on both sides. Each tube cord contains 2 pairs of flat suction cups. We will use 4 pair of flat suction cups in this study. We will place 2 pair on left and two on right para spinal muscles of lumber in prone lying. Due to its automatic suctioning capability, these cups can easily stick to skin. After placing the cups on lumber each patient of group A will receive its stimulation for about 10 minutes every day for about 4 weeks along with conventional exercises.

  • Conventional exercises

    Other intervention

    receive conventional exercises only. Conventional exercises will be performed for 20 minutes, each exercise will be performed 20 times with 10 seconds hold.

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: conventional exercisesExperimental treatment 1 intervention
Group B: Sadante neo therapyExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

McGill Pain Questionnaire:

The McGill Pain Questionnaire can be used to evaluate a person experiencing significant pain. It can be used to monitor the pain over time and to determine the effectiveness of any intervention.

Time frame
4th week

Secondary outcomes

1

Oswestry disability index:

This questionnaire has been designed to give us information as to how your back pain has affected your ability to manage everyday life

Time frame
4th week
2

Rand 36-items helath survey

The rand 36-items survey is used to indicate the health status of particular populations, to help with service planning and to measure the impact of clinical and social interventions

Time frame
4th week

Other outcomes

Sponsors and contacts

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