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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06387563
Other study ID # FUI/CTR/2024/4
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 6, 2023
Est. completion date May 30, 2024

Study information

Verified date April 2024
Source Foundation University Islamabad
Contact Iqra Ali, MS-MSKPT*
Phone 0316-5187052
Email iqraalianmol@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is a randomized control trial and the purpose of this study to determine the effects of abdominal muscle activation training on non-specific low back pain; using pressure biofeedback in comparison with surface electromyography biofeedback: a randomized control trial.


Description:

The purpose of this study is to determine the effects of abdominal muscle activation training, using pressure biofeedback in comparison with surface electromyography biofeedback, in management of non-specific low back pain: a randomized control trial. Pain and disability are the primary outcomes which will be determined using: 1. Numeric pain rating scale (NPRS) 2. Oswestry disability index (ODI) Data will be taken before and after the intervention protocol for each participant. Data collection procedure: Participants of interest would be approached and explained about the research. Informed written consent will be taken. Pre and post intervention scores will be recorded.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date May 30, 2024
Est. primary completion date May 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 44 Years
Eligibility Inclusion Criteria: - Age (adults 19 - 44 years) - Non-specific LBP with NPRS > 3 - Negative SLR test in prone and supine - Painless extremity movement and activity - Manual muscle testing of abdominal muscles between grade 2 - 4 - Sedentary individuals (no exercise plan followed in last 3 months) Exclusion Criteria: - History of any spinal surgery - Degenerative disc disorder, facet joint syndrome, spinal stenosis, myelopathy, lumbar syringomyelia - Sensory disturbances due to neurological causes, lumbar radiculopathy, fibromyalgia, myofascial pain syndrome - Sacroiliac joint dysfunction - Pregnancy - Medical conditions; Hypertension, Diabetes mellites - Work disability greater than 6 months - Not able to attend regular therapy appointments

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Abdominal activation using pressure biofeedback
PBF assisted abdominal muscle activation training (30 min, 3x /week /4 weeks) Progressive Muscle Relaxation for 5 min Pressure biofeedback assisted abdominal muscle activation training. Frequency: 25 min; 10 sec hold, 15 sec relax, 10 reps Progression criteria in training: Maintaining 3 - 5 mmHg pressure on PBF dial while performing abdominal muscle activation. Exercises for Group For biofeedback assisted abdominal muscle activation training these exercises will be performed: Supine abdominal muscle activation (45° Hip knee flexion) Both hip and knee 90° flexion One side hip and knee 90° flexion with other fully extended One side hip and knee 90° flexion with other fully extended + heel 12 cm raised Both legs fully extended with heel 12 cm raised Partial curl ups Prone lying abdominal muscle activation Prone leg raises Prone upper back extension simple Prone reciprocal UE/LE exercises
Abdominal activation using SEMG biofeedback
SEMG-BF assisted abdominal muscle activation training (30 min, 3x/ week/ 4 weeks) Progressive Muscle Relaxation for 5 min Surface EMG-BF assisted abdominal muscle activation training. Frequency: 25 min; 10 sec hold, 15 sec relax, 10 reps Maintaining minimal volumetric contraction of abdominal muscle activation (as per person) on SEMG device with abdominal muscle activation for set frequency Exercises for Group B For biofeedback assisted abdominal muscle activation training these exercises will be performed: Supine abdominal muscle activation (45° Hip knee flexion) Both hip and knee 90° flexion One side hip and knee 90° flexion with other fully extended One side hip and knee 90° flexion with other fully extended + heel 12 cm raised Both legs fully extended with heel 12 cm raised Partial curl ups Prone lying abdominal muscle activation Prone leg raises Prone upper back extension simple Prone reciprocal UE/LE exercises

Locations

Country Name City State
Pakistan Foundation University College of Physical Therapy Rawalpindi Punjab

Sponsors (1)

Lead Sponsor Collaborator
Foundation University Islamabad

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain Intensity The NPRS will be used to quantify LBP, and it exhibits good validity ranging from 0.79 to 0.95, as well as reliability ranging from 0.67 to 0.96(23). The scoring for NPRS involves a scale from 0 to 10, where 0 indicates no pain. The interpretation of scores is as follows: 0 to 3 for mild pain, 4 to 6 for moderate pain, and 7 to 10 for severe pain. 4 weeks
Primary Level of Disability For measuring disability, Oswestry Disability Index will be utilized 4 weeks
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