ClinicalTrials.Veeva

Menu

Integrated Neuromuscular Inhibition Versus Instrument Assisted Soft Tissue Mobilization in Chronic Back Pain

Cairo University (CU) logo

Cairo University (CU)

Status

Not yet enrolling

Conditions

Chronic Non Specific Low Back Pain

Treatments

Other: Experimental: Group B :Instrument assissted soft tissue mobilization
Other: Experimental: Group A: integrated neuromuscular inhibition technique
Other: control group C conventional physical therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT06116058
P.T.REC/012/004714

Details and patient eligibility

About

this study will be conducted to identify the difference between the effect of integrated neuromuscular inhibition technique and instrument assisted soft tissue mobilization on back pain, pain threshold, back rang of motion ,back proprioception and back disability in chronic non specific low back pain

Enrollment

45 estimated patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

    1. The patient's age ranged from 18 to 30 years.(Geogre et al, 2021) 2. Patients with low back pain for more than 3 months (pain felt between T12 and the gluteal fold).

    2. Patient with chronic low back pain 4. Normal body mass index from 18 -25kg/m2.

Exclusion criteria

  • The subjects will be excluded if they have any of the followings:

    1. Lumbar discogenic lesions or any inflammatory arthritis, tumors, infection involving the lumbar spine.
    2. Patients with decreased range of motion secondary to congenital anomalies, muscular contracture, or bony block.
    3. Previous lumbar or hip surgery or trauma.
    4. Any hip structural abnormality such as malformations, impingements and degeneration.
    5. Patients With cognitive impairments that would limit their participation

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

45 participants in 3 patient groups

Group A: integrated neuromuscular inhibition technique
Experimental group
Description:
Group A: patient will receive integrated neuromuscular inhibition technique and conventional physical therapy program for 3 sessions /week over 4 weeks periods
Treatment:
Other: Experimental: Group A: integrated neuromuscular inhibition technique
Group B :Instrument assissted soft tissue mobilization
Experimental group
Description:
Group B : patient will receive Instrument assissted soft tissue mobilization technique and conventional physical therapy program for 3 sessions /week over 4 weeks periods
Treatment:
Other: Experimental: Group B :Instrument assissted soft tissue mobilization
Group C:conventional physical therapy
Active Comparator group
Description:
Group C: patient will receive conventional physical therapy only in the form of ( stretch for hamstring ,illiopoaps ,low back muscle and strenghtning for abdominal ,back muscles and side support exercise and quadriped exercise)
Treatment:
Other: control group C conventional physical therapy

Trial contacts and locations

0

Loading...

Central trial contact

heba S mousa; Heba S mousa, master

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems