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Effect of Motor Control Exercise Combined With Laser Or TENS on Pain, Range of Motion, and Functional Disability on Obese Patients With Low Back Pain

Not Applicable
Completed
Conditions
Laser Therapy
Back Pain
Motor Control Exercises
Obesity
Interventions
Other: low-level laser therapy
Other: TENS
Other: motor control exercises
Registration Number
NCT06545578
Lead Sponsor
Ahram Canadian University
Brief Summary

This randomized study aimed to assess the impact of MCE in conjunction with LLLT and MCE in conjunction with TENS on pain levels, ROM, and functional disability in obese patients with LBP.

Detailed Description

Sixty obese male and female patients with LBP participated in this study. After providing informed consent, they were randomly divided into two equal groups, with Group A receiving MCE combined with LLLT and Group B receiving MCE combined with TENS.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria

The inclusion criteria were the following:

  • patients aged 40 to 77 years
  • non-athletic, have a BMI > 25
  • complaining of LBP.
Exclusion Criteria

The exclusion criteria were the following:

  • vertebral fractures
  • surgical spinal fixation
  • rheumatic disorders
  • any underlying medical condition that may be causing back pain, including:
  • malignancy
  • viscerogenic causes
  • infection, systemic disease of the muscles and skeletal system,
  • sensory dysfunction
  • neuromuscular diseases like multiple sclerosis.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Group (A):low-level laser therapyGroup A received motor control exercises with low level laser therapy
Group (B):motor control exercisesGroup B received motor control exercises with transcutaneous electrical nerve stimulation
Group (B):TENSGroup B received motor control exercises with transcutaneous electrical nerve stimulation
Group (A):motor control exercisesGroup A received motor control exercises with low level laser therapy
Primary Outcome Measures
NameTimeMethod
1- Assessment of lumbar flexion ROMbefore treatment and 4 weeks after treatment

The researcher positioned himself behind the patient standing to use his thumbs to identify the two posterior superior iliac spines (PSIS). He then delineated these two spines with a line on the skin, with the first mark located at the midpoint of the line and the second mark positioned 15 cm above. Subsequently, the researcher directed the patient to flex forward to the greatest extent possible while remaining within the boundaries of pain

the functional disability, the Oswestry disability questionnaire version 2.0before treatment and 4 weeks after treatment

Assessing functional disability in patients afflicted with LBP is accomplished with a valid and dependable instrument. There are six possible responses to each of the ten queries, which includes the daily functional disability. The patient chose the response that best described his impairment. Scores up to 50 are possible and are divided as follows: each question takes 5, the first statement takes 0, and the sixth statement takes 5 scores. The maximum score in this study was 45. All scores were subsequently tallied and converted to a percentage of the total score. A greater score is indicative of a severe disability. Scores between 0 and 20 represent minimal disability. Disability levels are classified as follows: scores between 40 and 60 indicate moderate disability; scores between 60 and 80 indicate disabled disability; and scores between 80 and 100 indicate bedridden patients

The pain was evaluated utilizing the visual analog scale (VAS)before treatment and 4 weeks after treatment

It comprises a 10-centimeter-long horizontal line secured at both ends with anchors. The initial anchor signifies the absence of pain, whereas the final anchor represents the most terrible pain. The patient was instructed to indicate the point through the line that most accurately represented the intensity of discomfort. The measurement was obtained by tracing the distance from the zero extremities to the patient's mark

2- Assessment of lumbar extension ROMbefore treatment and 4 weeks after treatment

Instructing the patient to bend backward to the best of his ability within the boundaries of pain, the investigator established a line on the skin and positioned himself behind the standing patient to distinguish between the two PSIS with his thumbs. The first mark was located at the midpoint of this line, and the second mark was positioned 15 cm above the first.

3- Assessment of lumbar side bending ROMbefore treatment and 4 weeks after treatment

As the patient assumed an erect position with heels, buttocks, and shoulders against the wall and a lateral bend without elevating the opposing foot off the ground, the investigator determined the distance between the third fingertip and the floor.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Ababa physical therapy center

🇪🇬

Banī Suwayf, Egypt

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