Efficacy of Vojta on Balance and Quality of Life in Subject With CNLBP
Primary Purpose
Chronic Non-Specific Low Back Pain
Status
Unknown status
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
conventional physical therapy
vojta therapy
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Non-Specific Low Back Pain
Eligibility Criteria
Inclusion Criteria:
- Patients with chronic non -specific low back pain for more than 3 months.
- Their age ranged between 18-35 years old
- Both sexes were recruited in this study.
- Their BMI ranged between 18-25 kg/m2
Exclusion Criteria:
1- Patients with previous spinal surgery 2. Patients who have radiological diagnosis of spondylolysis or spondylolisthesis.
3. Patient with neurological disease . 4. Chest problems 5. Systematic disease
Sites / Locations
- Mti UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
conventional treatment of back pain
vojta therapy
Arm Description
Group A: received conventional treatment of back pain which included; TENS 20 min and hot packs 10 min .The total treatment session is 30 min three session per week for four weeks
received conventional treatment of back pain in addition to Vojta therapy . The total treatment session is 40 min.
Outcomes
Primary Outcome Measures
static and dynamic balance
static and dynamic balance can assessed by using biodex balance system Each patient was instructed to maintain his/her balance for the period of the test.
There was report gained after finishing every test includes information on medial lateral stability index(MLSI), overall stability index(OSI), and anterior posterior stability index (APSI) measurements will done twice before and after treatment for all patients in both group
Oswestry Low Back Pain Disability Questionnaire
The Oswestry Low Back Pain Disability Questionnaire is an extremely important tool that researchers and disability evaluators use to measure a patient's permanent functional disability and quality of life. The test is considered the 'gold standard' of low back functional outcome tools measurements will done twice before and after treatment for all patients in both group
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04734314
Brief Title
Efficacy of Vojta on Balance and Quality of Life in Subject With CNLBP
Official Title
Effect of Vojta on Balance and Quality of Life in Subject With Chronic Non-spacific Low Back Pain
Study Type
Interventional
2. Study Status
Record Verification Date
April 2020
Overall Recruitment Status
Unknown status
Study Start Date
April 1, 2020 (Actual)
Primary Completion Date
February 5, 2021 (Anticipated)
Study Completion Date
February 5, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cairo University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
. To investigate the effect of Vojta method on static balance ,dynamic balance, quality of life in patients with chronic non - specific low back pain
Detailed Description
This randomized controlled trial is to investigate the effect of Vojta method on balance and quality of life in patients with chronic non-specific low back pain.
Forty patients (male and female) complaining of chronic non -specific low back pain was recruited to share in this study
. The recruited patients were randomly recruited into two groups; group A (control group) and group B (study group).
Group A: received conventional treatment of back pain which included; TENS 20 min and hot packs 10 min .The total treatment session is 30 min three session per week for four weeks Group B: received conventional treatment of back pain in addition to Vojta method. The total treatment session is 40 min.
Patient in both groups performed 10 sessions, 3 session per week
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Non-Specific Low Back Pain
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
45 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
conventional treatment of back pain
Arm Type
Experimental
Arm Description
Group A: received conventional treatment of back pain which included; TENS 20 min and hot packs 10 min .The total treatment session is 30 min three session per week for four weeks
Arm Title
vojta therapy
Arm Type
Experimental
Arm Description
received conventional treatment of back pain in addition to Vojta therapy . The total treatment session is 40 min.
Intervention Type
Other
Intervention Name(s)
conventional physical therapy
Intervention Description
conventional physical therapy in the form of transcutaneous electrical stimulation (TENS) for 20 min and hot pack for 10 min Each patient received 12 sessions three session per week.
Intervention Type
Other
Intervention Name(s)
vojta therapy
Intervention Description
Vojta Dynamic Neuromuscular Stabilization (DNS) is a therapy used to manage neurological and musculoskeletal conditions each patient in the study group (group B) was instructed to lie prone on an examination table with the participant's shoulders abducted, elbows flexed approximately 80-90°, and the forearms hanging off the edge of the table. Pressure-like stimulation of the calcaneus and ASIS were performed in the postural position named by Vojta as "reflex creeping.
Each patient received 12 sessions three session per week.
Primary Outcome Measure Information:
Title
static and dynamic balance
Description
static and dynamic balance can assessed by using biodex balance system Each patient was instructed to maintain his/her balance for the period of the test.
There was report gained after finishing every test includes information on medial lateral stability index(MLSI), overall stability index(OSI), and anterior posterior stability index (APSI) measurements will done twice before and after treatment for all patients in both group
Time Frame
one month
Title
Oswestry Low Back Pain Disability Questionnaire
Description
The Oswestry Low Back Pain Disability Questionnaire is an extremely important tool that researchers and disability evaluators use to measure a patient's permanent functional disability and quality of life. The test is considered the 'gold standard' of low back functional outcome tools measurements will done twice before and after treatment for all patients in both group
Time Frame
one month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Patients with chronic non -specific low back pain for more than 3 months.
Their age ranged between 18-35 years old
Both sexes were recruited in this study.
Their BMI ranged between 18-25 kg/m2
Exclusion Criteria:
1- Patients with previous spinal surgery 2. Patients who have radiological diagnosis of spondylolysis or spondylolisthesis.
3. Patient with neurological disease . 4. Chest problems 5. Systematic disease
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
walaa mohamed, B.Sc
Phone
01115640229
Email
dr-walaamohamed@hotmail.com
Facility Information:
Facility Name
Mti University
City
Cairo
Country
Egypt
Individual Site Status
Recruiting
12. IPD Sharing Statement
Learn more about this trial
Efficacy of Vojta on Balance and Quality of Life in Subject With CNLBP
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