The Effect of Structured Pain Education on Pain and Performance Parameters in Patients With Chronic Low Back Pain
Study Details
Study Description
Brief Summary
The Effect of Structured Pain Education on Pain and Performance Parameters in Patients with Chronic Low Back Pain
The aim of this study is to compare the effects of only Low Load Motor Control Exercises and Pain Education in addition to these exercises on pain, performance, disability and psychological factors, and to present a generalizable pain education in patients with chronic low back pain. We think that DYMK exercises applied together with a general Pain Education given to the patients will provide more improvement on these factors.
The patients will be divided into 2 groups, as a pain training group and an exercise group, with 20 people in each group, in a randomized controlled manner. Only DYMK exercise training will be applied to the exercise group. In the pain training group, pain training will be applied in addition to the DYMK exercise training.
As an evaluation parameter to the participants; Numerical Rating Scale, Short-Form McGill Pain Questionnaire, Pain Catastrophizing Scale, Tampa Kinesiophobia Scale, Roland-Morris Disability Questionnaire, Pain Self-Efficacy Questionnaire, Passive Lumbar Extension Test, Finger-Place Test and Physical Performance Test Battery will be applied. Patients will be evaluated before the start of the study (T0) and at the end of the study (T1).
Low Load Motor Control Exercises will be applied to people in both groups for 4 weeks, 3 days a week, during 20-30 minute sessions. In addition to the DYMK exercise training, a session of 30 to 50 minutes of Pain Training in groups of 4 to 5 people will be given to the patients included in the Pain Training group at the beginning of the exercise training and the exercise training will begin.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: exercise group Only DYMK exercise training will be applied to the exercise group. |
Other: exercise group
1 stage
In a sitting position, pull the leg up and extend the knee forward
Standing, bending forward and bending the knee
Supine, tucked legs
Maintaining spinal smoothness in crawling
Prone heel pull to buttock
Stage 2
Prone on forearms-hands
Extending the supine hands to the knees
Rounding and hollowing the waist in crawling
Progressive sit-stand
Standing up from sitting and putting on and taking off socks
Reaching up while standing and maintaining the straightness of the spine
Squatting
Climbing and descending stairs
Stage 3
Maintaining standing, arms forward
Slipping hands on the bed while standing
Initiating the standing throw and maintaining the position until the final interval
Putting on and taking off socks while standing
Taking weight towards the ground from a certain height
Picking up different weights from the ground
Push-pull items
Crossing obstacles of certain height
Walking a certain distance
|
| Experimental: pain training group In the pain training group, pain training will be applied in addition to the DYMK exercise training. |
Other: pain training group
The training provides participants with the opportunity to explain the central sensitization mechanism and also integrates the behavioral, psychological and environmental aspects that contribute to the persistence of pain. It is intended to teach that education reduces pain and improves endogenous pain inhibition, mental health, physical function, vitality and self-rated disability in patients with chronic pain, and reduces passive coping, kinesiophobia, and catastrophizing.
The same exercises will be applied as the exercise group.
|
Outcome Measures
Primary Outcome Measures
- Change from baseline of pain intensity on the Numerical Rating Scale at 3 weeks [baseline and 3 weeks]
It is an 11-point unidimensional measure of pain intensity. It is a segmented numerical version of the Visual Analog Scale (VAS), in which participants select an integer (0-10 integer) that best reflects the intensity of their pain. 0 represents no pain and 10 represents worst pain.
- Change from baseline in the multidimensional measure of pain on the Short-Form McGill Pain Questionnaire at 3 weeks [baseline and 3 weeks]
A multidimensional measure of pain. It consists of 2 subscales: 1) a sensory subscale consisting of 11 words or items, and 2) an emotional subscale consisting of 4 items rated on the intensity scale (0= none, 1= mild, 2= moderate, and 3= severe). It also includes 1 item for current pain intensity and 1 item for 10 cm Visual Analog Scale for mean pain.
- Change from baseline in assessing feelings, thoughts, and emotions related to pain and disaster on the Pain Catastrophizing Scale at 3 weeks [baseline and 3 weeks]
It is used to assess the patient's feelings, thoughts, and feelings about pain and disaster. It is a self-administered questionnaire with 13 items and 3 subscales: helplessness, magnification, and rumination. A 5-point scale is used for each item, with higher values representing greater destruction. The scores of each item are added to determine the subscales and the total score is calculated with the sum of all items. Scores range from 0 to 52 points.
- Change from baseline in measuring fear of movement and (re)injury on the Tampa Kinesiophobia Scale at 3 weeks [baseline and 3 weeks]
A 17-item questionnaire that measures fear of movement and (re)injury. Each question is answered on a 4-point Likert scale ranging from "strongly disagree" to "strongly agree". The total score is calculated after reversing the individual scores of items 4, 8, 12, and 16.
- Change from baseline in questioning pain-related disability from low back pain on the Roland Morris Disability Questionnaire at 3 weeks [baseline and 3 weeks]
A 24-item self-reported outcome measure questioning pain-related disability from low back pain. Items are scored 0 if left blank or 1 if approved. The total score ranges from 0 to 24; higher scores represent higher pain-related disability.
- Change from baseline in the patient's ability to perform a range of activities despite pain in the Pain Self-Efficacy Questionnaire at 3 weeks [baseline and 3 weeks]
A 10-item questionnaire that measures both the strength and generality of a patient's beliefs about their ability to perform a range of activities despite pain. Scores can range from 0 to 60, with higher scores indicating stronger self-efficacy beliefs.
- Measuring pain intensity and disability in the Revised Graded Chronic Pain Scale at baseline [baseline]
The new scale, consisting of 6 questions, was developed as a revised version of the original scale. There is a categorical rating scheme and numerical self-assessment scores for pain intensity and disability. The first 2 questions ask the frequency of pain, how the pain affects life and work activities and evaluate the last 3 months. It is scored from 0 to 4 (0 = never to 4 = every day). Questions between 3 and 5 (PEG scale) evaluate the severity of pain in the last 7 days and are scored between 0-10 points. The third question questions the severity of the pain. Questions 4 and 5, respectively, ask how pain interferes with enjoying life and how it affects general activities. Question 6 has 2 answers (1=yes and 2=no) and asks if the person is not working or unable to work because of pain or painful condition.
- Change from baseline in assessing internal factors and emotions influencing the experience of health-threatening physical injury and pain in the Pain Beliefs Questionnaire at 3 weeks [baseline and 3 weeks]
The consists of two subscales. The organic beliefs subscale (PBQ-O) questions the user about physical injury or physiological pain that threaten wellness, while the psychological pain beliefs subscale (PBQ-P) evaluates intrinsic factors and emotions affecting the pain experience that may potentially threaten wellness.
- Identifying subjective neuropathic pain experience on the Pain Perception Questionnaire at baseline [baseline]
It is a symptom-based assessment tool performed by clinicians to specify the subjective neuropathic pain experience of patients.
- Change from baseline in assessing overall quality of Sleep at 3 weeks [baseline and 3 weeks]
It's about the overall quality of sleep about most nights in the last 7 days. It is scored between 1 and 10. High scores represent good sleep quality.
Secondary Outcome Measures
- Change from baseline in detecting structural lumbar segmental instability on Passive Lumbar Extension Test at 3 weeks [baseline and 3 weeks]
It is a passive test that detects structural lumbar segmental instability. Participants are placed in a prone position and the physiotherapist then lifts both lower extremities simultaneously to a height of approximately 30 cm from the bed while keeping the knees extended and gently pulling the legs. The test is considered positive if the participant reports low back pain during testing.
- Change from baseline on trunk mobility on the Finger-Place Test at 3 weeks [baseline and 3 weeks]
It is a test that provides information about trunk mobility. The participant stands upright on a 20 cm high platform, with shoes off and feet glued together. He is asked to bend forward as much as possible, fully extending his knees, arms and fingers. The vertical distance between the tip of the middle finger and the platform is measured with a flexible tape measure and expressed in centimeters. The vertical distance between the platform and the tip of the middle finger is considered positive when the participant does not reach the platform, and negative when they can go further.
- Change from baseline in maintaining a neutral lumbar spine in the Physical Performance Test Battery at 3 weeks [baseline and 3 weeks]
Includes bias bridge, side bridge, Biering-Sørensen test and a motion control test battery. . All tests will be performed in standard positions. In the bias bridge, side bridge and Biering-Sørensen testing, emphasis will be placed on maintaining a neutral lumbar spine for as long as possible (seconds).
Eligibility Criteria
Criteria
Inclusion Criteria:
-
18 to 65 years old
-
Chronic low back pain 3 days a week and ≥ 3 months
-
Absence of spinal fracture or acute disc herniation
-
Absence of existing psychiatric problems and mental deficiencies
-
Absence of exercise contraindications [28] [29] [30]
Exclusion Criteria:
-
Being diagnosed with lumbar radiculopathy
-
Pain due to tumors or infections, metastases, osteoporosis, inflammatory arthritis or fractures
-
Specific medical conditions (neck or back surgery in the previous 3 years, osteoporotic vertebral fractures or rheumatological diseases)
-
Chronic widespread pain syndromes (fibromyalgia or chronic fatigue syndrome)
-
Receiving any other treatment for chronic low back pain during the study [28] [29] [30]
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Istanbul Medipol University Sefakoy Hospital | Istanbul | Turkey | 34515 |
Sponsors and Collaborators
- Medipol University
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- MedipolUniversity