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The Effect of Breathing Exercise and Stabilization Exercise With Chronic Low Back Pain

Not Applicable
Completed
Conditions
Sleep Hygiene
Low Back Pain
Anxiety
Interventions
Device: Conventional physical therapy
Other: Lumbar stabilization exercises
Other: Breathing exercises
Registration Number
NCT05212753
Lead Sponsor
Hasan Kalyoncu University
Brief Summary

The aim of this study is to compare the effect of sleep hygiene, breathing exercises, and stabilization exercises on pain, sleep quality, and anxiety level in patients with non-specific chronic low back pain.

Detailed Description

Addressing sleep problems in patients with chronic non-specific low back pain (LBP) can reduce chronic pain, the risk of developing depressive illness and improve pain-related quality of life.

Sleep is a concept that has physiological, psychological, and social dimensions. Sleep is one of the essential and indispensable daily life activities that affect individuals' quality of life and well-being. Decreasing pain is expected and likely to improve sleep quality. Still, it is unknown what will happen due to improving sleep quality to resolve the pain of unknown origin.

Education about sleep hygiene with physiotherapy has not been assessed before on individuals with nonspecific LBP. Since this training will require a lifestyle change, individuals should be warned not once but several times in a certain time, and this training should be reinforced. This will be an advantage for the patients receiving physiotherapy, and their therapists will support them in applying this training during the physiotherapy sessions.

In our study, individuals with nonspecific chronic low back pain will be divided into three groups using the blinding method as part of a randomized controlled trial.

The first group, as the conventional physical therapy group, will receive a hot pack and TENS only.

The second group, as the stabilization group, will receive lumbar stabilization exercises and the conventional physical therapy program.

The third group, as the breathing exercise group, will receive breathing exercises, including sleep hygiene and stabilization group program.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
48
Inclusion Criteria
  • individuals between the ages of 18-65
  • Having low back pain for at least the last 3 months
  • Pain at 4 out of 10 according to VAS (Visual Analogue Scale)
Exclusion Criteria
  • Radiculopathies
  • Body mass index > 35
  • Neurological, orthopedic, or cardiopulmonary diseases that will contraindicate exercise
  • Treatment for pain in the last 3 months who have received
  • individuals who can't cooperate and those who have problems adapting to exercises

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Conventional Physical Therapy GroupConventional physical therapyThe conventional physical therapy group will receive Transcutaneous Electrical Nerve Stimulation (TENS) and hot pack application.
Breathing Exercise GroupBreathing exercisesThe breathing exercise group will receive breathing exercises including sleep hygiene, and the stabilization group program. Breathing exercises include diaphragmatic breathing and pursed-lip.
Breathing Exercise GroupConventional physical therapyThe breathing exercise group will receive breathing exercises including sleep hygiene, and the stabilization group program. Breathing exercises include diaphragmatic breathing and pursed-lip.
Stabilization GroupConventional physical therapyThe stabilization group will receive lumbar stabilization exercises and the conventional physical therapy program. That program includes lumbar stabilization exercises including activation of the transverses abdominals (TA) and multifidi muscles.
Stabilization GroupLumbar stabilization exercisesThe stabilization group will receive lumbar stabilization exercises and the conventional physical therapy program. That program includes lumbar stabilization exercises including activation of the transverses abdominals (TA) and multifidi muscles.
Breathing Exercise GroupLumbar stabilization exercisesThe breathing exercise group will receive breathing exercises including sleep hygiene, and the stabilization group program. Breathing exercises include diaphragmatic breathing and pursed-lip.
Primary Outcome Measures
NameTimeMethod
Change from Baseline in Pain at 3 weeks and 8 weeksBaseline, 3 weeks, 8 weeks

Visual Analogue Scale will be used where patients will be asked to rate their pain on a scale from 0 to 10 with 0 indicating no pain and 10 the maximum worst pain, at the baseline and the end of 3 weeks intervention and at the end 8 weeks from baseline.

Change from Baseline in Form of Pain at 3 weeks and 8 weeksBaseline, 3 weeks, 8 weeks

Form of Pain will be assessed with the Mcgill Melzack Pain Questionnaire. The questionnaire consists of four parts. In the first part, the individual marks the place where they feel pain on a representative body picture and indicates with the letters "D" if the pain is deep, "S" if it is on the body surface, and "D-S" if it is both deep and superficial. In the second part, there are 20 statements that examine pain from various aspects. The individual is asked to choose the word group that fits their pain and to marks only one word in the selected group that fits their pain. In the third part, there are questions about the relationship between time and pain. In the fourth part, five word-groups ranging from "mild to unbearable" pain are defined to determine the severity of pain.

Change from Baseline in Anxiety at 3 weeks and 8 weeksBaseline, 3 weeks, 8 weeks

Anxiety will be assessed with the Spielberger State-Trait Anxiety Inventory. It consists of two separate scales, each with 20 questions, assessing the levels of state anxiety and trait anxiety. The score that can be obtained from both scales is a minimum of 20 and a maximum of 80. If the score from the scale is high, the person's anxiety is high.

Change from Baseline in Sleep Quality at 3 weeks and 8 weeksBaseline, 3 weeks, 8 weeks

Sleep quality will be assessed with the Pittsburgh Sleep Quality Index (PSQI). PSQI is a 19-item self-report questionnaire that measures subjective sleep quality over the previous month. The individual 19 items in the PSQI are aggregated into seven components that assess various aspects of sleep, and the sum of these seven components yields a score that distinguishes between "good" and "bad" sleepers.

Change from Baseline in Fatigue at 3 weeks and 8 weeksBaseline, 3 weeks, 8 weeks

Fatigue will be assessed with the Fatigue Severity Scale.

This scale consists of 9 items in total. Individuals give points from 1 to 7 for each item. If the average score is greater than 6.1, it is concluded as chronic fatigue.

Secondary Outcome Measures
NameTimeMethod
Obstructive Sleep Apnea Risk Screening İn İndividuals With Chronic Non-Specific Low Back PainBaseline

Stop-Bang Survey, used as a screening tool for obstructive sleep apnea (OSAS), is a questionnaire consisting of 8-item yes/no responses with a score for each positive answer.

Moderate risk of OSAS: yes to 3-4 questions, and high risk of OSAS: yes to 5-8 questions.

Trial Locations

Locations (1)

İslahiye İlçe Hast.

🇹🇷

Gaziantep, Turkey

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