- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04000685
The Effects of Different Exercise Approaches in Patients With Chronic Low Back Pain
June 1, 2023 updated by: Muzeyyen Oz, Hacettepe University
The Effects of Different Exercise Approaches on Physical and Cognitive Variables in Patients With Chronic Low Back Pain
Identification of the effects of yoga, stabilization exercise and aerobic exercise approaches on physical and cognitive variables in individuals with low back pain.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Patients participating in the study were divided three parallel groups.
The patients in the stabilization exercise group were instructed to perform spinal stabilization exercises, the patients in the yoga group were instructed to perform yoga program consisting of breathing, relaxation and flexibility exercises.
The patients in the aerobic exercise group were instructed to perform aerobic walking training.
The severity of the pain evaluated through visual analog scale, functional status and quality of life, alexithymia, kinesiophobia, catastrophic pain, back awareness, cognitive function evaluated through Oswestry Disability Index(ODI), Nottingham Health Profile (NHP), Toronto Alexithymia Scale, Fear Avoidance Beliefs Questionnaire, Pain Catastrophizing Scale, Fremantle Back Awareness Scale, Montreal Cognitive Assessment respectively.
Assessments were repeated before and after the treatment.
Study Type
Interventional
Enrollment (Actual)
81
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Altındag
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Ankara, Altındag, Turkey, 06100
- Hacettepe University, Faculty of Physical Therapy and Rehabilitation
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
25 years to 55 years (Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Non-specific low back pain
- Must be pain at least 3 months
Exclusion Criteria:
- History of any lumbar spine surgery
- Presence of neurological deficit
- Having been diagnosed with cardiovascular or systemic diseases that would prevent him / her from taking exercise training.
- The presence of persistent severe pain
- Pain below the knee
- Severe/progressive scoliosis
- Spinal stenosis
- Spondylolisthesis
- Cancer
- Diabetes
- Metabolic syndrome
- Inflammatory, infectious or tumoral disease of the vertebra
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Yoga exercise group
Yoga program were applied all patients in this group accompanied by physiotherapist.
Sessions included selected breathing, warm up and relaxation exercises.
|
Yoga exercise program will be applied two sessions per week, totally eight week.
|
|
Active Comparator: Spinal stabilization exercise group
Spinal stabilization exercise with three different progressive phases were applied all patients in this group accompanied by physiotherapist.
|
Spinal stabilization exercise program will be applied two sessions per week, totally eight week.
|
|
Active Comparator: aerobic walking exercise group
Aerobic walking exercise program applied all patients in this group accompanied by physiotherapist.
|
Aerobic walking program will be applied two sessions per week, totally eight week.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in pain severity
Time Frame: change from baseline in pain severity at 8 weeks
|
Patients' average resting, activity and night pain intensities assessed by Visual Analog Scale.
The visual analog scale is an 11-point scale ranging from 0 to 10, in which 0 defines absence of pain and 10 describes unbearable pain.
Participants asked to rate the average pain levels a horizontal 10 cm straight line on a white sheet from, before and after treatment.
|
change from baseline in pain severity at 8 weeks
|
|
Changes of functional status
Time Frame: change from baseline in functional status at 8 weeks
|
Patient's permanent functional disability measured by Oswestry Disability Index.
The scale is considered the 'gold standard' of low back functional outcome tools.
This scale contain questions related to functional activities of pain intensity, personal care, lifting, walking, sitting, standing, sleeping, sex life, social life and travelling.Interpretation of scale are 0% to 20% for minimal disability, 21% to 40% for moderate disability, 41 % to 60 % for severe disability 61% to 80 % for crippled and 81 % to 100 % Bed-bound.
|
change from baseline in functional status at 8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in quality of life
Time Frame: Change from baseline in life quality levels at 8 weeks
|
Health-related quality of life assessed by Nottingham Health Profile (NHP).
The NHP contain 38 questions in 6 subareas: pain, physical abilities, energy level, sleep, social isolation and emotional reaction.
The scores range from 0 to 100, with each question assigned a weighted value; the sum of all weighted values in a given subarea adds up to 100.
Lower scores denoting a better quality of life.
|
Change from baseline in life quality levels at 8 weeks
|
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Changes in gait parameters
Time Frame: Change from baseline in gait parameters at 8 weeks
|
Gait assessment will be recorded with OptoGait for one minute while participants walked their preferred speed on the treadmill.
Patients asked to walk on level surface.
Assessment were recorded during one minute.
|
Change from baseline in gait parameters at 8 weeks
|
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Changes in metabolic capacity
Time Frame: Change from baseline in metabolic capacity at 8 weeks
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Metabolic capacity testing will be performed according to the Modified Bruce protocol on the Treadmill.
At 3 minute intervals, the inclination increase by %2 with a concomitant increase in speed.
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Change from baseline in metabolic capacity at 8 weeks
|
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Changes in cognitive level
Time Frame: Change from baseline in cognitive level at 8 weeks
|
The Montreal Cognitive Assessment Questionnaire (MoCA) will be used to assess the cognitive levels of individuals.
MoCA was developed as a rapid screening test for mild cognitive impairment.
MoCA assesses various cognitive functions such as attention and concentration, creative functions, memory, language, visual structuring skills, abstract thinking, computation and orientation.
The application of MoCA takes about 10 minutes.
The maximum total score of the test is 30.
A score of 21 or above is considered normal.
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Change from baseline in cognitive level at 8 weeks
|
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Changes in alexithymia
Time Frame: Change from baseline in alexithymia at 8 weeks
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The alexithymia will be assessed by the Toronto Alexithymia Scale (TAS).
The scale is a Likert-type self-assessment scale consisting of 20 items and scored between 1-5.
Difficulties in recognizing emotions (TAS-1), difficulty in speaking emotions (TAS-2), extroverted thinking (TAS-3) subscales.
The individual is asked to select the best option for each item from "Never", "Rarely", "Sometimes", "Often" and "Always".
The higher the score, the higher the level of alexithymia.
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Change from baseline in alexithymia at 8 weeks
|
|
Changes in kinesiophobia.
Time Frame: Change from baseline in kinesiophobia at 8 weeks
|
Fear-Avoidance-Beliefs Questionnaire will be applied to evaluate kinesiophobia which is fear of movement due to low back pain.This questionnaire has 2 sub-sections related to physical activity and work.
There are 4 questions scored in the physical activity section and 7 questions in the work section.
0-6 points are obtained for each question.
The total score will be recorded.
The higher the score, the higher the kinesiophobia.
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Change from baseline in kinesiophobia at 8 weeks
|
|
Changes in back awareness
Time Frame: Change from baseline in back awareness at 8 weeks
|
The Fremantle Back Awareness Questionnaire will be used to evaluate how individuals perceive the back according to their body.
The questionnaire includes 9 questions that measure how individuals perceive their back according to their body and how they perceive their body position.
Questions is answered Likert type as "0" I never feel like this, "4" always or often feel like this.
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Change from baseline in back awareness at 8 weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Ozlem Ulger, Prof, Hacettepe University
- Principal Investigator: Muzeyyen OZ, MSc, Hacettepe University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Chang DG, Holt JA, Sklar M, Groessl EJ. Yoga as a treatment for chronic low back pain: A systematic review of the literature. J Orthop Rheumatol. 2016 Jan 1;3(1):1-8.
- Inani SB, Selkar SP. Effect of core stabilization exercises versus conventional exercises on pain and functional status in patients with non-specific low back pain: a randomized clinical trial. J Back Musculoskelet Rehabil. 2013;26(1):37-43. doi: 10.3233/BMR-2012-0348.
- Meng XG, Yue SW. Efficacy of aerobic exercise for treatment of chronic low back pain: a meta-analysis. Am J Phys Med Rehabil. 2015 May;94(5):358-65. doi: 10.1097/PHM.0000000000000188.
- Koldas Dogan S, Sonel Tur B, Kurtais Y, Atay MB. Comparison of three different approaches in the treatment of chronic low back pain. Clin Rheumatol. 2008 Jul;27(7):873-81. doi: 10.1007/s10067-007-0815-7. Epub 2008 Jan 11.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 30, 2019
Primary Completion (Actual)
May 1, 2023
Study Completion (Actual)
May 1, 2023
Study Registration Dates
First Submitted
June 23, 2019
First Submitted That Met QC Criteria
June 26, 2019
First Posted (Actual)
June 27, 2019
Study Record Updates
Last Update Posted (Estimated)
June 2, 2023
Last Update Submitted That Met QC Criteria
June 1, 2023
Last Verified
June 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- KA-19029
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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