The Effect of Structured Pain Education on Pain and Performance Parameters in Patients With Chronic Low Back Pain

NCT05331274 | Unknown

• 1 other identifier: MedipolUniversity
• Study Type: interventional
• Target: 35
• Locations: 1 country
• Sites: 1

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.

Conditions

Chronic Low Back Pain

Outcome Measures

Primary Outcomes (10)

• Change from baseline of pain intensity on the Numerical Rating Scale at 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.

  baseline and 3 weeks

• Change from baseline in the multidimensional measure of pain on the Short-Form McGill Pain Questionnaire at 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.

  baseline and 3 weeks

• Change from baseline in assessing feelings, thoughts, and emotions related to pain and disaster on the Pain Catastrophizing Scale at 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.

  baseline and 3 weeks

• Change from baseline in measuring fear of movement and (re)injury on the Tampa Kinesiophobia Scale at 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.

  baseline and 3 weeks

• Change from baseline in questioning pain-related disability from low back pain on the Roland Morris Disability Questionnaire at 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.

  baseline and 3 weeks

• 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

  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.

  baseline and 3 weeks

• Measuring pain intensity and disability in the Revised Graded Chronic Pain Scale at 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.

  baseline

• 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

  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.

  baseline and 3 weeks

• Identifying subjective neuropathic pain experience on the Pain Perception Questionnaire at baseline

  It is a symptom-based assessment tool performed by clinicians to specify the subjective neuropathic pain experience of patients.

  baseline

• Change from baseline in assessing overall quality of Sleep at 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.

  baseline and 3 weeks

Secondary Outcomes (3)

• Change from baseline in detecting structural lumbar segmental instability on Passive Lumbar Extension Test at 3 weeks

  baseline and 3 weeks

• Change from baseline on trunk mobility on the Finger-Place Test at 3 weeks

  baseline and 3 weeks

• Change from baseline in maintaining a neutral lumbar spine in the Physical Performance Test Battery at 3 weeks

  baseline and 3 weeks

Study Arms (2)

exercise group

EXPERIMENTAL

Only DYMK exercise training will be applied to the exercise group.

Other: exercise group

pain training group

EXPERIMENTAL

In the pain training group, pain training will be applied in addition to the DYMK exercise training.

Other: pain training group

Interventions

exercise group OTHER

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

exercise group

pain training group OTHER

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.

pain training group

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• 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 \[28\] \[29\] \[30\]

You may not qualify if:

• 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 \[28\] \[29\] \[30\]

Sponsors & Collaborators

• Medipol University: lead

Study Sites (1)

Istanbul Medipol University Sefakoy Hospital

Istanbul, 34515, Turkey (Türkiye)

RECRUITING

Central Study Contacts

Ayşe Yaşar

CONTACT

+90 5073018156; ayseyasar48@hotmail.com

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: physiotherapist

Study Record Dates

• First Submitted: March 15, 2022
• First Posted: April 15, 2022
• Study Start: April 15, 2022
• Primary Completion: June 15, 2022
• Study Completion: October 30, 2022
• Last Updated: May 17, 2022

Record last verified: 2022-05

Data Sharing

• IPD Sharing: Will not share

Locations

TU (1)