Effectiveness of Treadmill Walk on Chronic Low Back Pain

Sponsor
Bayero University Kano, Nigeria (Other)
Overall Status
Recruiting
CT.gov ID
NCT05102097
Collaborator
(none)
40
1
2
16.7
2.4

Study Details

Study Description

Brief Summary

Chronic low back pain is a common health problem with a multifactorial impact on core muscle function as well as causing pain, functional disability and decrease in quality of life, this occur due to the reduction in the physical activity level of the individual causing atrophy and inhibition of the core muscle affecting the stability of the spine

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Warm-up
  • Behavioral: Main exercise
  • Behavioral: Cool down
  • Behavioral: Standard of care
N/A

Detailed Description

There are several approaches and methods of treating chronic low back pain (CLBP) ranging from education, exercise, electrotherapy and Manual therapy; to alternative treatment such as acupuncture, yoga and Chiropractic. Among the above mention treatment exercise, manual therapy and education are the most frequently utilize for the management of CLBP. The general recommendation for individual with CLBP is to remain active as possible and this can be achieve through exercise.

Evidence shows that active treatment in form of strengthening exercise of the abdominal and back muscles, core stabilization exercise, coordination exercise and aerobic exercise leads to significant reduction in pain and functional disability in patients with CLBP. A number of researches have been focusing on core stability exercise, which is an effective way of recruiting the core muscle (including the abdominal, back, pelvic and hip muscles) that leads to the optimal force production, control of lumbopelvic-hip movement and load transfer from the spine to the pelvis and the lower extremities. The core stabilization exercise has been establish to activate and strength the deep core muscles, but researches are now focusing on the exercise that can be able to activate the core muscles as well as increase the overall health status of the individual

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Group A (experimental group) participants in this group will walk on treadmill and perform standard of care in form of exercises. Group B (Control Group) participants in this group will receive standard of care aloneGroup A (experimental group) participants in this group will walk on treadmill and perform standard of care in form of exercises. Group B (Control Group) participants in this group will receive standard of care alone
Masking:
Single (Outcomes Assessor)
Masking Description:
Upon completion of baseline assessments, participants will be randomly assigned into two groups A and B in 1:1 ( i.e 20 participants per group) ratio using table of random digit generated from excel. The study will be single-blind whereby only the outcome assessors will be blinded to participant's group allocation but the type of intervention will not be specified. Because of the nature of the intervention it will be difficult to blind the participants.
Primary Purpose:
Treatment
Official Title:
Effectiveness of Treadmill Walk on Clinical and Functional Variables of Chronic Low Back Pain Patients
Actual Study Start Date :
Aug 16, 2021
Anticipated Primary Completion Date :
Oct 7, 2022
Anticipated Study Completion Date :
Jan 5, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental Group

Treadmill walk: i- warm up ( 5 minutes ) II- Main exercise (30 minutes) III- cool down (5 minutes) IV- Standard of care (10minutes)

Behavioral: Warm-up
Participants will walk on treadmill at a speed of 1.7 mile per hour (MPH) and 0 inclination each session for 6weeks 3 times in a week

Behavioral: Main exercise
Participants will walk on a treadmill with a starting speed of 1.7 mile per hour with inclination of 1 to 4% starting with 1% and increased by 1% each week until 4 weeks and at week 5 and 6 speed will be increased to 5mile per hour starting from 1.7mile per hour and increased by 0.5 mile per hour each 1minute while inclination will be increased to 5% in week 5 and 6% in week 6. Main exercise will be perform 3 times in a week for 6 weeks

Behavioral: Cool down
Participants will walk on treadmill at the speed of 1.7 mile per hour 0 inclination each session for 6 weeks 3 times in a week

Behavioral: Standard of care
Participants will perform Abdominal hollowing, isometric back extension exercise, bridging exercise, graded active flexion, graded active extension by holding for 5seconds and repeated 10times

Active Comparator: Control group

Standard of care (10 minutes)

Behavioral: Standard of care
Participants will perform Abdominal hollowing, isometric back extension exercise, bridging exercise, graded active flexion, graded active extension by holding for 5seconds and repeated 10times

Outcome Measures

Primary Outcome Measures

  1. Numeric pain rating scale [5minutes]

    A scale of 0 to 10 with 0 indicating no pain and 10 worst pain will be administered to the participants to choose a number indicating their level of pain this will be recorded at base line and 6 weeks after intervention

  2. Electromyograph [10minutes]

    Muscle activity of both lumbar multifidus muscle and rectus abdominous muscle will be assess using neurotrac myoplus pro machine and surface electrode. The assessment will be done both at baseline and at 6weeks after intervention

  3. Biering-sorensen test [3 minutes]

    Participant in prone position stabilize at both ankle and hip with the upper trunk out of the plinth will be instructed to extend the trunk and hold position, the more the time the participant is able to hold the position the more the core muscle endurance

  4. Abdominal dynamic test [3 minutes]

    Participants in supine lying position with the knees flexed to 90 degrees and upper limbs across the chest will be instructed to raised the trunk and neck and hold the position this will be timed using stopwatch. The more the time the participant is able to hold the position the more the core muscle endurance

  5. Flexion rotation test [3 minutes]

    Participants in supine position the knees flex the participants will be instructed to touch alternate knees for 90 seconds and number of repetition will be recorded. The higher the number of repetition the more the core muscle endurance

  6. Pressure biofeedback stabilizer [4 minutes]

    Pressure biofeedback stabilizer will be use to assess the strength of rectus abdominous and Lumbar multifidus muscle strength, the pressure biofeedback stabilizer is a simple device that sense changes in pressure with movement, the pressure cell measures from 0-200millimeter of mercury (mmHg), with a precision of 2 millimeter of mercury with 0 being the lowest score and 200 the highest score. To measure any of the core muscle strength the pressure biofeedback stabilizer will be inflated to 70 millimeter of mercury and will be placed underneath the muscle of the participant and instruction will be giving to the participant to contract the muscle by pressing the inflator down, the reading on the sphygmomanometer will then be recorded.

Secondary Outcome Measures

  1. Oswestry disability index [10 minutes]

    This questionnaire will be administered to the participant both English and hausa version will be use pending on the preference of the participant will be ask to fill so as to know their level of functional disability at baseline and 6 weeks after administration. The questionnaire is scored from 0 indicating no disability and 100 maximum disability

  2. Short form health survey questionnaire [10 minutes]

    Short form health survey questionnaire will be administered to the participants the English or Hausa version pending on the participant preference and their quality of life will be assessed both at baseline and 6weeks intervention. The questionnaire will be scored from 0 to 100, with 0 indicating poor quality of life and 100 highest score in terms of quality of life

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • male and females between the age of 18 to 65years

  • participants attending Usmanu Danfodiyo University teaching Hospital, Sokoto State Specialist Hospital and Orthopedic Hospital

  • participants with chronic non-specific low back pain

Exclusion Criteria:
  • participants with current low back pain for less than 12 weeks

  • participants with cognitive and visual impairment

  • participants with other co-morbidities ( systemic disease, carcinomas, organ disease)

  • Participants with other neurological findings such as loss of sensation, radiculopathy, parenthesis

  • Body mass index of more than 30 Kilogram per meter square

  • participants who are pregnant

  • participants who had spinal surgery

Contacts and Locations

Locations

Site City State Country Postal Code
1 Usmanu Danfodiyo University Teaching Hospital Sokoto Sokoto Nigeria 840102

Sponsors and Collaborators

  • Bayero University Kano, Nigeria

Investigators

  • Principal Investigator: Rahanatu A Abba, Msc, Usmanu Danfodiyo University Teaching Hospital Sokoto, Nigeria

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Rahanatu Abubakar Abba, Principal Investigator, Bayero University Kano, Nigeria
ClinicalTrials.gov Identifier:
NCT05102097
Other Study ID Numbers:
  • SPS/18/MPT/00018
First Posted:
Nov 1, 2021
Last Update Posted:
Jul 20, 2022
Last Verified:
Oct 1, 2021
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 Rahanatu Abubakar Abba, Principal Investigator, Bayero University Kano, Nigeria
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 20, 2022