Skip to content

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

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06987175
Enrollment
40
Registered
2025-05-23
Start date
2025-05-15
Completion date
2025-07-31
Last updated
2025-07-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low Back Pain, Pain, Range of Motion

Keywords

sedante neo therapy, non specific low back pain, quality of life

Brief summary

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.

Detailed description

This study is to evaluate SADANTE neo therapy on pain, range of motion and quality of life in patients with low back pain. This study will identify the effects that will help the physiotherapists in making the treatment plan for low back pain. This can be an alternative non pharmacological therapy to improve the quality of pain management with maximum benefits and minimal side effects.

Interventions

OTHERConventional exercises

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

OTHERsadante neo therapy

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.

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Weeks to 40 Weeks
Healthy volunteers
No

Inclusion criteria

* 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) * Having ODI score 5 to 24 * Having SF-36 healty survey score below 50 * Having range of motion below normal.

Exclusion criteria

* 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 -Open sores * Psychiatric diseases such as depression, phobias * Patient with history of surgery in lumber region

Design outcomes

Primary

MeasureTime frameDescription
McGill Pain Questionnaire:4th weekThe 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.

Secondary

MeasureTime frameDescription
Oswestry disability index:4th weekThis questionnaire has been designed to give us information as to how your back pain has affected your ability to manage everyday life
Rand 36-items helath survey4th weekThe 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

Countries

Pakistan

Contacts

Primary Contactimran amjad, Phd
imran.amjad@riphah.edu.pk03324390125

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026