Clinical Trials Logo

Back Pain clinical trials

View clinical trials related to Back Pain.

Filter by:

NCT ID: NCT02226692 Completed - Clinical trials for Chronic Low Back Pain

Prognostic Factors of Disabling Low Back Pain in Patients With Chronic Low Back Pain

Start date: October 2011
Phase: N/A
Study type: Observational

The aim of the present study is to quantify the relative contribution of variables obtained during a physical fitness evaluation and a short screening questionnaire in determining the short-term and long term risk of persistent disabling low back pain in patients with chronic low back pain. It has been hypothesized that patients with higher physical fitness will present a lower risk of persistent disabling low back pain and so, a lower score on the questionnaire.

NCT ID: NCT02225535 Completed - Clinical trials for Chronic Low Back Pain

Investigation of a Physiotherapist and Nurse Practitioner Intervention for Chronic Low Back Disorders Delivered Through Telehealth

Start date: July 2014
Phase: N/A
Study type: Interventional

The purpose of this project is to compare "usual care" for chronic low back disorders in a rural setting (nurse practitioner/NP) to two different means of integrating Physical Therapy (PT) into a rural health care team: 1. in-person PT assessment, where the PT travels from an urban center 2. interprofessional Telehealth assessment where the local NP is joined by a PT via Telehealth. The project will evaluate health, systems and process outcomes, comparative effectiveness and costs of the three methods of assessment. The hypothesis is that an interprofessional Telehealth assessment with be as effective as an in-person PT assessment, but more effective than usual care.

NCT ID: NCT02224183 Completed - Clinical trials for Recurrent Low Back Pain

Yoga vs. Education for Veterans With Chronic Low Back Pain

Start date: March 2015
Phase: N/A
Study type: Interventional

Chronic low back pain (cLBP) is the most common pain condition in the military, causing substantial physical and psychological suffering, reduction in force readiness, and high economic cost. Yoga has been studied in 10 RCTs in civilian populations with cLBP suggesting it may be effective in reducing pain intensity, improving back-related function, and lowering pain medication use. Multiple differences exist between civilian and military populations with cLBP, making it necessary to adapt and test yoga for cLBP in military populations. This study's primary aim is to evaluate the effectiveness of yoga for reducing pain in military personnel and Veterans with cLBP through a structured, reproducible 12-week series of hatha yoga classes, supplemented with home practice, compared to an education group. Additionally, the enormous mental health burden often shouldered by returning military personnel presents another important distinguishing factor. Thus, the study's secondary aim is to assess yoga's capacity to reduce post-traumatic stress symptoms (PTSS). The third aim is to evaluate the cost-effectiveness of yoga for cLBP at 3 months and 6 months from the perspective of the provider, the Veteran, and the Veterans Health Administration. The fourth and final aim is to evaluate the effect of back pain and yoga on marital and family functioning. The proposed RCT will (1) establish a structured reproducible yoga protocol uniquely suited to Veterans populations with cLBP; (2) develop web-based delivery systems to assist Veterans in yoga home practice; (3) increase our knowledge of the feasibility and impact of yoga for Veterans' cLBP and psychological comorbidities. These results will help determine whether yoga is an effective modality for addressing cLBP in a Veteran population.

NCT ID: NCT02221609 Completed - Low Back Pain Clinical Trials

Movement System Impairment Based Classification Versus General Exercise for Chronic Non-specific Low Back Pain: a Randomised Controlled Trial

Start date: October 2014
Phase: N/A
Study type: Interventional

The objective of this study is to investigate the efficacy of a treatment based on Movement System Impairment based classification (MSI) model in patients with chronic non-specific low back pain.

NCT ID: NCT02220543 Completed - Chronic Pain Clinical Trials

Chronic Low Back Pain Rehabilitation in Primary Care: an RCT

Start date: August 2014
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the effectiveness and cost-effectiveness of a new primary care intervention "Back on Track" as compared to usual primary care in patients with non-specific chronic low back pain in which disability levels are moderate and the role of psychosocial factors to this disability is at maximum low (classified as WPN2).

NCT ID: NCT02203448 Completed - Clinical trials for Chronic Low Back Pain

Facet Wedge Post Market Study

Start date: May 1, 2014
Phase:
Study type: Observational

A Multi-centre, Prospective, single-arm post market clinical follow up study (PMCF) of the FACET WEDGETM spinal system to assess outcomes in subjects with chronic low back pain due to Degenerative Disc Disease (DDD), facet joint disease and/or pseudo arthrosis post anterior instrumentation. The objective of this study is to assess outcomes following implantation of the FACET WEDGE spinal system when used to provide fixation of lumbar motion segments. The primary objective of this study is to determine the rate of re-operations at the index level(s). The secondary objectives of this study are to confirm the safety and performance of the device and to collect patient reported outcome data.

NCT ID: NCT02196129 Completed - Clinical trials for Low Back Pain With Radiculopathy

Immediate Pain Relieving Effects of Sinbaro-3 for Low Back Pain

Start date: July 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate the immediate pain relieving effects of sinbaro-3 pharmaco-acupuncture in patients with low back pain admitted for inpatient care

NCT ID: NCT02180776 Completed - Back Pain Clinical Trials

Effectiveness of Inelastic LSO Versus Standard Medical Treatment for Back Pain Associated With Kyphosis

ARISE
Start date: June 2012
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate clinical effectiveness and the effect on quality of life of an inelastic thoracolumbarasacral orthosis in male and female hyperkyphotic patients with moderate to severe back pain disability and to demonstrate the safety of the intervention through detailed reporting and analysis of adverse events.

NCT ID: NCT02170753 Completed - Low Back Pain Clinical Trials

Regional Manual Therapy and Motor Control Exercise for Chronic Low Back Pain

Start date: June 2014
Phase: N/A
Study type: Interventional

Purpose: The primary purpose of this study is to determine whether or not the addition of thoracic, pelvic, and hip manual therapy to a standard physical therapy (PT) approach consisting of motor control exercises and lumbar spine manual therapy is better than standard PT alone at improving thoracolumbar spine range of motion (ROM), hip ROM, pain intensity, disability level, and perceived change in patients with chronic low back pain (CLBP) and movement coordination impairments. Hypothesis: In a CLBP subgroup with movement coordination impairments, participants receiving thoracic, pelvic, and hip manual therapy with standard PT will be superior to participants receiving standard PT alone at improving thoracolumbar spine ROM, hip ROM, pain intensity, physical disability level, and perceived change at two, four, and 12 weeks after initiating treatment.

NCT ID: NCT02168582 Completed - Low Back Pain Clinical Trials

Improvement After Physiotherapy for Low Back Pain: The Good Responders

Start date: May 2014
Phase:
Study type: Observational

This is an observational study that aims to characterize individual response of patients getting physical therapy for chronic non-specific low back pain. Participants will be classified based on a questionnaire and motor tests to investigate whether individual improvement after physical therapy may be predicted. These observations may help to decide which should be the preferred treatment offered.