Effectiveness of Pressure Biofeedback Therapy and Progressive Muscle Relaxation Technique in Improving Pain and Disability Among Patients With Non-Specific Low Back Pain

Sponsor
Dow University of Health Sciences (Other)
Overall Status
Recruiting
CT.gov ID
NCT05616702
Collaborator
(none)
70
1
2
13.4
5.2

Study Details

Study Description

Brief Summary

Low back pain is common MSK disease with prevalence of 60 to 70 percent. Patients with low back discomfort are typically treated conservatively by physical therapists. Progressive muscles relaxation technique has been shown in several studies to reduce chronic back pain and increase flexibility. pressure biofeedback therapy works on Intra abdominal pressure.it helps to alleviate compression on lumbar spine and support the adjacent lumbar spine.The aim of this randomized controlled trial is to determine the effectiveness of pressure biofeedback training (Pr.BFB) in combination with progressive muscles relaxation technique (PMR) & progressive muscles relaxation training alone on pain, disability, ROM & endurance of muscles among nonspecific chronic low back pain patients.

Condition or Disease Intervention/Treatment Phase
  • Other: Pressure Biofeedback Therapy + Progressive Muscles Relaxation + thermotherapy
  • Other: Progressive Muscles Relaxation + thermotherapy
N/A

Detailed Description

A randomized clinical trial will be carried out in the Physical Therapy O.P.D of Dow hospital Karachi. Collection of data will commence right after approval of synopsis from Dow IRB. A sample of 70 NSCLBP patients calculated by using mean & SD of visual analogue scale in abdominal stabilisation training with Pr.BFB stabilizer was 2.69 ±0.93 and Progressive muscular Relaxation VAS was 3.863 ±2.03. Before being recruited into the experiment, patients will be screened to ensure that they meet the inclusion criteria. Pain rating scale and Roland-Morris questionnaire will be used to gather data after explaining the research goals to patients and obtaining formal consent from them. Patients will be divided into 2 interventional groups by simple random sampling, with 35 patients in each group. Experimental group will be received Pressure Bio-Feedback Therapy in combination with PMR Technique and Thermotherapy. The Control group, on the other hand, will be received a combination of Progressive Muscle Relaxation Technique and Thermotherapy for non-specific CLBP. It will be a 6-weeks intervention plan with 3 sessions per week (40-minutes each). Assessor will be blinded to the treatment. Roland Morris Low back pain and disability questionnaire (RMQ) and the NPR Scale will be used as primary outcome measures. Secondary outcomes will be determined by modified-modified Schober test for assessing lumbar ROM & Pressure Biofeedback Stabilizer unit helps to gauge muscular endurance.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
70 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Effectiveness of Pressure Biofeedback Therapy and Progressive Muscle Relaxation Technique in Improving Pain and Disability Among Patients With Non-Specific Low Back Pain
Actual Study Start Date :
Oct 15, 2022
Anticipated Primary Completion Date :
Oct 16, 2023
Anticipated Study Completion Date :
Nov 27, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Pressure Biofeedback Therapy + Progressive Muscle Relaxation Technique + Thermotherapy.

This study ARM will receive following therapies Pressure Biofeedback Therapy Progressive Muscles Relaxation Technique Thermotherapy

Other: Pressure Biofeedback Therapy + Progressive Muscles Relaxation + thermotherapy
Pressure Biofeedback Therapy prone position, abdominal drawing in for 10 sec. (PBU inflated to 70 mmHg) Supine position with flexed knees, abdominal drawing in for 10 sec. (PBU inflated to 40 mmHg) Progress to leg loading in supine abdominal drawing in for 10 sec. (PBU inflated to 40 mmHg) Exercising dosage: Duration: 15 mins Frequency: 3 sessions/ week Repetitions: 3 sets of 15 reps Progressive Muscles Relaxation Technique Tense => five seconds and, release => ten seconds (Each group of muscle) 2 circuits daily Exercising dosage: Duration: 15 mins Frequency: weekly 3 sessions; for 6 weeks Repetitions: 2 reps (cycles) Thermotherapy at lumbar region via electrical heating pad Duration: 15 mins

Active Comparator: Progressive Muscle Relaxation Technique + Thermotherapy

This study ARM will receive following therapies Progressive Muscles Relaxation Technique Thermotherapy

Other: Progressive Muscles Relaxation + thermotherapy
Progressive Muscles Relaxation Technique Tense => five seconds and, release => ten seconds (Each group of muscle) 2 circuits daily Exercising dosage: Duration: 15 mins Frequency: weekly 3 sessions; for 6 weeks Repetitions: 2 reps (cycles) Thermotherapy at lumbar region via electrical heating pad Duration: 15 mins

Outcome Measures

Primary Outcome Measures

  1. Numeric Pain Rating Scale (change is being assessed) [Baseline and 6 weeks]

    On a scale of 0 to 10, "Please indicate the intensity of current, best, and worst pain levels over the past 24 hours on a scale of 0 (no pain) to 10 (worst pain imaginable)"

  2. Roland-Morris Low Back Pain and Disability Questionnaire (change is being assessed) [Baseline and 6 weeks]

    A standard tool called the "Roland-Morris Disability Questionnaire" consists of 24 items about a person's disabilities and pain perceptions The patient is told to draw a mark beside each element that corresponds to him or her. Sum of marked items will determine a patient's score. The scoring ranges from 0 - 24. (No to extreme disability).

Secondary Outcome Measures

  1. Endurance test (change is being assessed) (mmHg) [Baseline and 6 weeks]

    For evaluating the functionality of deep abdominals via Pressure Biofeedback Unit , a standard device that monitors changes in pressure, allowing for muscle contraction and detection of spinal mobility during exercise.

  2. Endurance test (change is being assessed) (hold time in seconds) [Baseline and 6 weeks]

    For evaluating the functionality of deep abdominals via Pressure Biofeedback Unit , a standard device that monitors changes in pressure, allowing for muscle contraction and detection of spinal mobility during exercise.

  3. Lumbar Range of Motion (cm) (change is being assessed) [Baseline and 6 weeks]

    Modified- Modified Schober test For patients with low back discomfort, MMST method appears to be a good method for evaluating lumbar flexion and extension.

Eligibility Criteria

Criteria

Ages Eligible for Study:
30 Years to 50 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Diagnosed and referred patients with non-specific low back pain for more than 3 months

  • 30 to 50 years

  • Both genders

Exclusion Criteria:
  • Any surgical history of lumbar spine

  • Infections of the spine, malignancy

  • Disc protrusion

  • History of spinal fractures

Contacts and Locations

Locations

Site City State Country Postal Code
1 Dow Institute of Physical Medicine and Rehabilitation, DUHS. Karachi Sindh Pakistan 74200

Sponsors and Collaborators

  • Dow University of Health Sciences

Investigators

  • Study Director: Farhan I Khan, Ph.D, MBA, MSc.PT, DPT, Dow University of Health Sciences

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Shaiaza Masooma, Principal Investigator, Dow University of Health Sciences
ClinicalTrials.gov Identifier:
NCT05616702
Other Study ID Numbers:
  • 2694
First Posted:
Nov 15, 2022
Last Update Posted:
Nov 17, 2022
Last Verified:
Nov 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Shaiaza Masooma, Principal Investigator, Dow University of Health Sciences
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 17, 2022