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Chronic Low Back Pain clinical trials

View clinical trials related to Chronic Low Back Pain.

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NCT ID: NCT04529096 Completed - Clinical trials for Chronic Low-back Pain

Chronic Pain Master Protocol (CPMP): A Study of LY3016859 in Participants With Chronic Low Back Pain

Start date: August 25, 2020
Phase: Phase 2
Study type: Interventional

This study is being done to test the safety and efficacy of the study drug LY3016859 for the treatment of chronic low back pain. This trial is part of the chronic pain master protocol H0P-MC-CPMP (NCT05986292) which is a protocol to accelerate the development of new treatments for chronic pain.

NCT ID: NCT04520334 Completed - Clinical trials for Chronic Low Back Pain

A Zhineng Qigong Intervention for Patients With Chronic Low Back Pain and/or Leg Pain

Start date: November 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate a Zhineng Qigong intervention for patients with chronic low back pain and/or leg pain, and to test feasibility aspects.

NCT ID: NCT04518891 Recruiting - Clinical trials for Chronic Low-back Pain

Cognitive Functional Therapy Compared With Sham-treatment for Low Back Pain

Start date: May 17, 2021
Phase: N/A
Study type: Interventional

Chronic low back pain is a public health problem, and there is strong evidence that it is associated with a complex interaction of biopsychosocial factors. Cognitive functional therapy (CFT) is a promising new intervention that deals with potentially modifiable multidimensional aspects of pain (eg, provocative cognitive, movement and lifestyle behaviors). In order to better understand the contextual effects, the aim of the current study is to investigate the efficacy of CFT compared with a sham-intervention for pain intensity and disability post-intervention in patients with non-specific chronic low back pain (CLBP). This study is a randomized clinical trial (RCT) in which 152 (18 - 60 years old) patients with CLBP will be enrolled. The patients will be randomly allocated to receive: (1) CFT intervention or (2) sham-intervention. The experimental group will receive individualized CFT in a pragmatic manner (5 to 7 sessions) based on the clinical progression of participants. The sham group will attend six sessions: consisted of 30 minutes of photobiomodulation using a detuned device and more 15 minutes of talking about neutral topics. Participants will be assessed pre and post-intervention, three months and six months after randomization. Patients from both groups also will receive an educational booklet. The primary outcomes will be pain intensity and disability post-intervention. The secondary outcomes will be: pain intensity and disability at 3- and 6-month follow-up, as well as self-efficacy, global perceived effect of improvement and functioning post-intervention, 3- and 6-month follow-up. The patients and the assessor will be blinded to treatment administered (active vs. sham). The between-group differences (effects of treatment) and their respective 95% confidence intervals will be calculated by constructing linear mixed models. Treatment effect for the primary and secondary outcomes will be estimated using mixed linear models. To the best of our knowledge, the current study will be the first to compare CFT vs. sham intervention. Sham-controlled RCTs may help to understand the influence of non-specific factors on treatment outcomes. Considering complex interventions as CFT, it is imperative to understand the impact of contextual factors on outcomes.

NCT ID: NCT04494698 Active, not recruiting - Opioid Use Clinical Trials

Impact of DuoTherm on Opioid Use and Chronic Low Back Pain

Start date: June 23, 2022
Phase: N/A
Study type: Interventional

Evaluate opioid use and pain change in chronic Low Back Pain with DuoTherm Compared to Active Control

NCT ID: NCT04483128 Completed - Chronic Pain Clinical Trials

Electrical Stimulation With Interferential Current in the Non-especific Chronic Low Back Pain: Effects on the Autonomic Nervous System.

Start date: June 1, 2020
Phase: N/A
Study type: Interventional

The aim of this study it's to analyze the relationship between autonomic nervous system balance (ANSb) and chronic pain conditions, especially in this case, non-especific chronic low back pain (CLBP). Most of physiotherapy approaches focus only in biomechanical aspects, leaving aside what kind of factors could perpetuate CLBP. Since 1985, ANSb was studied due to its potential contribution to chronic pain. Electrical stimulation, through interferential currents (IFC), it's a safe and well-known therapy used in CLBP with good outcomes regarding pain relief. The main objective of this study it's to quantify the association between CLBP and ANSb alterations. In second place, the research team aims to record the influence of IFC over pain and ANSb in those subjects.

NCT ID: NCT04479787 Completed - Neuropathic Pain Clinical Trials

Spinal Cord Stimulation vs. Medical Management for Low Back Pain (DISTINCT)

Start date: July 31, 2020
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the efficacy of BurstDR dorsal column stimulation, compared with conventional medical management, in improving pain and back-related physical function in subjects suffering with chronic, refractory axial low back pain with a neuropathic component, who have not had lumbar spine surgery and for whom surgery is not an option.

NCT ID: NCT04406363 Not yet recruiting - Clinical trials for Chronic Low-back Pain

Confinement Effect on Low Back Pain Intensity in Chronic Low Back Pain Patients

CONFI-LOMB
Start date: June 2, 2020
Phase:
Study type: Observational

The current situation, linked to the pandemic of the new coronavirus SARS-CoV-2 generates health concerns, but is also accompanied by many other psychological, social, economic, professional, etc. consequences as well as numerous changes in behavior and lifestyles, notably due to confinement. While the prevention of chronic low back pain and its management are primarily based on the practice of regular physical and sports activity, other psychological factors (stress, anxiety, depression), socioeconomic (low level of education, resources), professionals (physical workload, job dissatisfaction), etc. also have a major role in the onset and the persitence of low back pain. Thus, it is to be supposed that the current context, and more particularly the confinement to which the population has been constrained for almost 2 months, have and will have notable consequences on the evolution of lumbar symptoms in chronic low back pain patients. However, the entanglement of different factors related to containment will potentially have different consequences depending on the individual. It therefore seems difficult to predict how the lumbar symptoms will develop in this population. Indeed, if it can imagined that the decrease in regular physical activity and the increase in anxiety in this context of insecurity could lead to an increase in pain, it could just as well consider that the decrease in stress work, strenuous physical work or travel time from work to home can, on the contrary, have a favorable effect. The objective of this study is to assess the confinement effect on low back pain intensity in chronic low back pain patients. This is an observational, descriptive, transversal and pluricentric study conducted by a single questionnaire.

NCT ID: NCT04399772 Completed - Clinical trials for Chronic Low-back Pain

COgNitive FuncTional Therapy+ for Chronic Low Back paIn

CONFeTTI
Start date: September 27, 2020
Phase: N/A
Study type: Interventional

This study is a patient-blinded 2-arm randomized controlled trial (RCT) assessing the effectiveness (in the short and long term) as well as total healthcare costs of a CFT+ (a combined physiotherapist/psychologist intervention) pathway compared with interdisciplinary pain management pathway (usual care) for patients with chronic low back pain referred to interdisciplinary pain treatment. The primary aim of this pragmatic randomized controlled trial (RCT) is to investigate if a physiotherapy-led CFT pathway that includes psychologist support (CFT+) with the option of additional usual care (if needed) is superior to the currently recommended interdisciplinary pain management pathway (usual care) in reducing disability at 12 months in patients with severe cLBP. In addition, an economic evaluation will investigate total health care costs of the two pathways at 12 months. In addition the study will explore changes in pain intensity, quality of life, thoughts and beliefs about back pain, and analgesic consumption in patients randomized to the CFT+ pathway compared with patients randomized to the interdisciplinary pain management pathway.

NCT ID: NCT04378413 Completed - Clinical trials for Chronic Low-back Pain

Aquatic and Land Exercises in Chronic Low Back Pain

Start date: November 2, 2019
Phase: N/A
Study type: Interventional

Aquatic and Land Exercises on Chronic Low Back Pain

NCT ID: NCT04342130 Completed - Clinical trials for Chronic Low-back Pain

Brain Effects of Opiate Agonist and Antagonist

Start date: April 27, 2018
Phase: Phase 4
Study type: Interventional

This study will look at the short-term effect of morphine on brain response to food.