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Back Pain clinical trials

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NCT ID: NCT06139848 Completed - Clinical trials for Non-specific Low Back Pain

Comparison of Posterior-anterior Spinal Mobilization and Prone Press up in Patients With Non Specific Low Back Pain

Start date: May 22, 2023
Phase: N/A
Study type: Interventional

No previous literature found on the comparison of posterior-anterior spinal mobilization and prone press-up on pain, range of motion and disability in patients with non-specific low back pain. This study will approach the results of posterior- anterior spinal mobilization and prone press-up on pain, range of motion and disability in patients with non-specific low back pain. In previous researches the patients were not properly followed to see pre session, immediate after the session and after twenty- four hours effects of both interventions Posterior- anterior mobilization and Press-ups. Secondly, they have not taken the control group in their studies. In current study two techniques along with conventional treatment will be compared in three different groups to see their individual effects and combine effect of Maitland and Mackenzie technique

NCT ID: NCT06133855 Completed - Clinical trials for Mechanical Low Back Pain

Impact of Electromagnetic Field Therapy on Pain and Function in Patients With Mechanical Back Pain

Start date: December 1, 2023
Phase: N/A
Study type: Interventional

This study aims to investigate the impact of electromagnetic field therapy on pain severity and functional disability in mechanical back pain patients suffering from myofascial trigger points.

NCT ID: NCT06129305 Completed - Pain, Postoperative Clinical Trials

Erector Spina Muscle Distance From the Skin at Different Thoracal Elevations

Start date: September 6, 2021
Phase:
Study type: Observational

In our study, we aimed to calculate the ideal measurement of the distance of the erector spina muscle to the skin and to find the best ultrasonography image at different thoracic levels (T1-T2, T5-T6, T5-T6, T11-T12) and in other positions (lateral-sitting-pron) to improve the quality of the block in patients who will undergo erector spina plan block. Our primary goal is to determine which thoracic level the erector spinae muscle is closer to the skin and whether the USG screen image is better. Our secondary goal is to find out in which position the erector spinae muscle is closer to the skin and the USG screen image is better.

NCT ID: NCT06125496 Completed - Low Back Pain Clinical Trials

Relationship Between Kinesiophobia, Physical Activity and Disability Level and Pain Management in Patients With CLBP

Start date: December 25, 2019
Phase:
Study type: Observational

The aim of this study was to examine the relationship between pain management, kinesiophobia, physical activity and disability level in patients with chronic low back pain (CLBP) in different genders. Eighty-two patients with CLBP (42 females, 42 males) between the ages of 20-60 participated in the study. Pain management strategies were determined by Pain Coping Questionnaire (PCQ). Tampa Scale for Kinesiophobia for perception of kinesiophobia, Oswestry Disability Index for disability due to pain and International Physical Activity Questionnaire-Short Form (IPAQ-SF) for the physical activity level were used.

NCT ID: NCT06120959 Completed - Pregnancy Related Clinical Trials

Effect of Adding Pelvic Floor Exercises to the Stabilization Exercises in Treating Low Back Pain During Pregnancy

Start date: January 1, 2023
Phase: N/A
Study type: Interventional

The purpose of the study is to know the effect of adding pelvic floor exercises to the stabilization exercises in treating low back pain during pregnancy.

NCT ID: NCT06109116 Completed - Clinical trials for Nonspecific Low Back Pain

Effects of Self-myofascial Release on Hamstring Flexibility in Patients With Non Specific Low Back Pain

Start date: October 1, 2023
Phase: N/A
Study type: Interventional

The aim of this preliminary study suggest the addition of self myofascial release to a therapeutic exercise program in reducing hamstring flexibility and would have additional effects on decreasing pain intensity in individuals with non specific low back pain.

NCT ID: NCT06099860 Completed - Clinical trials for Sacroiliac Joint Dysfunction

Therapeutic Impact of KT Along With BT in Patients With Chronic Low Back Pain of Sacroiliac Joint Dysfunction

Start date: November 14, 2022
Phase: N/A
Study type: Interventional

This research aimed to determine the impacts of KT and balance exercises in patients with CLBP of SIJ dysfunction.

NCT ID: NCT06099470 Completed - Clinical trials for Chronic Non-specific Low Back Pain

Investigation of the Effects of Telerehabilitation Groups for Chronic Non-specific Low Back Pain.

Start date: June 1, 2023
Phase: N/A
Study type: Interventional

The goal of this study is to investigate the efficacy of different internet based delivery methods for patients with chronic non-specific low back pain. The parameters we want to study is pain, disability, fear of movement, and quality of life.

NCT ID: NCT06098053 Completed - Back Pain Clinical Trials

Efficacy of Muscle Energy Technique Alone and in Combination With Interferential Therapy for the Treatment of Non-specific Low Back Pain.

Start date: May 21, 2023
Phase: N/A
Study type: Interventional

Single blind randomized control trail in which two groups were formed. Group A was given Muscle energy technique and Group B was given muscle energy technique in combination with Interferential therapy.

NCT ID: NCT06082375 Completed - Clinical trials for Chronic Low-back Pain

Supplementation With Vitamin D3 on Chronic Low Back Pain Patient

Start date: August 1, 2019
Phase: N/A
Study type: Interventional

The study was designed as a randomized double-blind placebo-controlled clinical trial with 8-week Vitamin D3 and physical activity intervention. The protocol was approved by Independent Bioethics Committee for Scientific Research at Medical University of Gdańsk (No. 525/2018), in accordance with the Declaration of Helsinki. We enrol 40 patient (aged ≥ 35), Patients diagnosed with chronic pain in the lumbar spine, qualified for surgical treatment at the Department of Neurosurgery Medicinal Unit in Gdańsk. Participation in the study was voluntary, and the condition for participation was obtaining informed consent from the patient.