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Back Pain clinical trials

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NCT ID: NCT02112760 Completed - Clinical trials for Recurrent Low Back Pain

Specific Stabilization Exercise With Ultrasound Feedback For Patient With Recurrent Low Back Pain

Start date: June 2011
Phase: N/A
Study type: Interventional

1. Specific aim 1:Identify factors that influence muscle performance by use of ultrasound imaging. Hypothesis: Gender, age, and BMI affect the muscle performance of deep trunk muscles. 2. Specific aim 2. To compare the performance of trunk deep muscles (transversus abdominis and multifidus) and the sensation and pain thresholds of patients with recurrent low back pain with asymptomatic subjects. Hypothesis: patients with recurrent low back pain have: (A) less activation of the transversus abdominis and multifidus, (B) peripheral and central sensitization, with decreased sensation and pain thresholds in the lumbar and foot areas. 3. Specific aim 3. To determine the performance of the transversus abdominis and multifidus, and the sensation and pain thresholds by use of ultrasound feedback training in asymptomatic adults, and to compare these results with the traditional training protocols for trunk stabilization. Hypothesis: Specific stabilization exercise using ultrasound feedback training is more effective in activating deep trunk muscles and increasing sensation and pain thresholds than the traditional stabilization training protocol in asymptomatic adults. 4. Specific aim 4. To determine the performance of the transversus abdominis and multifidus, and the sensation and pain thresholds by using the ultrasound feedback training in adults with low back pain, and to compare these results with the traditional training protocols for trunk stabilization. Hypothesis: Specific stabilization exercise using ultrasound feedback training is more effective in activating deep trunk muscles and increasing sensation and pain thresholds than the traditional stabilization training protocol in adults with low back pain.

NCT ID: NCT02111278 Completed - Low Back Pain Clinical Trials

Lumbar Manipulation and Exercise for the Treatment of Acute Low Back Pain in Adolescents

Start date: May 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if the addition of lumbar manipulation will improve function, decrease pain, and recurrence in adolescents with low back pain. The secondary aim of this study is to determine if a modification of a clinical prediction rule by Flynn will be effective in identifying adolescent patients with low back pain who would benefit from lumbar manipulation.

NCT ID: NCT02106741 Completed - Fatigue Clinical Trials

Acupressure for Fatigue and Low Back Pain

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

The purpose of this study is to compare two kinds of self-administered acupressure (relaxation acupressure and stimulating acupressure) to usual care for management of fatigue and pain in low back pain patients. Hypothesis: Self-administered relaxation acupressure will result in improvements in fatigue and sleep quality, pain, and physical function compared to stimulating acupressure and usual care.

NCT ID: NCT02093793 Completed - Chronic Pain Clinical Trials

Safety and Effectiveness Study of the Precision SCS Systems Adapted for High-Rate Spinal Cord Stimulation

ACCELERATE
Start date: March 27, 2014
Phase: N/A
Study type: Interventional

To evaluate the safety and effectiveness of the Precision Spinal Cord Stimulator Systems Adapted for High-Rate Spinal Cord Stimulation as an aid in the management of chronic intractable pain

NCT ID: NCT02090686 Completed - Clinical trials for Chronic Low Back Pain

Pulsatile Cupping in Low Back Pain

Cupping-LBP
Start date: March 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether pulsatile cupping with a cupping device is effective in the treatment of patients with chronic low back pain compared to no cupping or to minimal cupping.

NCT ID: NCT02089750 Completed - Clinical trials for Chronic Low Back Pain

Orthotic Use for Chronic Low Back Pain

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

The goal of this randomized clinical study is to assess pain and dysfunction in 225 volunteer subjects who have chronic low back pain. The hypothesis of this study is that custom-made shoe will improve patients' low back pain and dysfunction. Additionally, custom-made shoe orthotics plus chiropractic treatment will further improve patients' low back pain and dysfunction while maintaining that improvement during the one year study follow-up period. Specific Aims: 1. To determine the changes in perceived pain levels (Numeric Pain Rating Scale) and dysfunction (Oswestry Disability Index) in patients with chronic low back pain after six weeks of custom-made shoe orthotic use with or without chiropractic care as compared to no care. 2. To determine the changes in perceived pain levels and dysfunction in patients with chronic low back pain after twelve weeks of custom-made shoe orthotic use. 3. To determine the changes in perceived pain levels and dysfunction at 3, 6, and 12 months following the 12 week treatment period.

NCT ID: NCT02089321 Completed - Low Back Pain Clinical Trials

Multiplanar Lumbopelvic Control in Patients With Low Back Pain

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

The purpose of this study was to investigate whether combined assessment of lumbopelvic control during sagittal and frontal plane motion (using two common clinical observational assessments) discriminates between people with and without LBP than single plane assessment alone. It was hypothesized that the two tests used in combination (multiplanar) would perform better than each test used independently (single planar) in accurately discriminating patient cases from healthy controls.

NCT ID: NCT02088463 Completed - Clinical trials for Low Back Pain, Mechanical

Mobilization for Post Partum Low Back Pain

Start date: December 2012
Phase: N/A
Study type: Interventional

The study was conducted to the following purposes 1. To investigate the effect of lumbar mobilization on muscle activity in postpartum mechanical low back pain. 2. To investigate the effect of lumbar mobilization on pain intensity in postpartum mechanical low back pain patients. 3. To investigate the effect lumbar mobilization on functional disability in postpartum mechanical low back pain patients. 4. To compare between the effects of lumbar mobilization, tactile stimulation (placebo treatment) and traditional treatment in postpartum mechanical low back pain patients.

NCT ID: NCT02073292 Completed - Clinical trials for Chronic Thoracic Back Pain

Cooled Radiofrequency Ablation vs. Thermal Radiofrequency Ablation

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

Nerves in your body transmit signals to and from your brain and the cells in your body. In the event of an injury or disease, these nerves transmit pain. Sometimes, when an injury doesn't heal, chronic pain can develop. One way to treat chronic pain is to interrupt these pain signals. One method of doing this is to use Radio frequency ablation (RFA). Radio frequency ablation (RFA) is a medical procedure in which heat is generated from high frequency electrical current in order to lesion (burn) nervous tissue. Radiofrequency ablation is used to treat many conditions in several areas of the body including cardiac (heart) as well as chronic pain. Probes (needles) are inserted into the body to a specific location and the electrical current is passed through these needles. This electrical current creates heat in your body and forms small lesions or burns in a specific place. Doctors will use tools, such as fluoroscopy (x-rays) and injections to locate the specific nerves that are transmitting pain and then use the electrical current to destroy those nerves. Equipment used include generator, built in nerve stimulator, different needles and probes and water cooling system in case of the cooled RFA. There are several types of probes or needles that are used to transmit energy and create lesions. This study is going to compare 2 types - standard radiofrequency and 'cooled' radiofrequency. The only difference is that the 'cooled' radiofrequency probes have water running through the probe tip, which keeps the tip cool and allows a larger lesion to be made. Since the doctor can't actually see the nerve he is trying to target, the larger lesion should theoretically improve his chances of hitting it. The 'cooling' of the water also allows the temperatures to be lower than what is needed for standard RF. In this study, the investigators would like to compare the differences between standard RFA (90°C) and "cooled" RFA (60°C) ablation techniques and determine if one is better for pain relief. All of the probes that are used to perform radiofrequency ablation are FDA approved and are commonly used to treat patients with chronic back pain. Participating in the study involves being randomly assigned to received either standard or cooled RFA. The procedure for both standard and cooled RFA is basically the same. The only difference is with standard RFA, the doctor may perform up to 2 lesions, instead of 1 if they are using cooled RFA. Both study groups will receive local anesthetic prior to procedure. The treating doctor will use a machine called a C-Arm to take x-rays. These x-rays will guide the doctor to be sure the probes are in the right place. Once the probe placement is confirmed, the doctor will turn on the generator and create the lesion. This process will be repeated depending on how many lesions need to be created. After the procedure there will be follow up visits at 1, 3 and 6 months. Level of pain, health and recovery information will be collected.

NCT ID: NCT02067494 Completed - Low Back Pain Clinical Trials

Myofascial Release and Kinesio Taping on Autonomic Nervous System in Low Back Pain

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

The purpose of this current randomized clinical trial is to determine the effects of myofascial soft tissue release and kinesio taping on disability, pain, quality of life, autonomic nervous system and oxidative stress indicators in chronic low back pain.