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Low Back Pain clinical trials

View clinical trials related to Low Back Pain.

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NCT ID: NCT06461494 Not yet recruiting - Low Back Pain Clinical Trials

Comparison of Egoscue Versus Pilates Exercises in Patient With Mechanical Low Back Pain

Start date: June 2024
Phase: N/A
Study type: Interventional

Mechanical low back pain arises intrinsically from the spine, intervertebral disc,or surrounding soft tissues.It is causes by muscular spasm, and other soft tissue injuries. The aim of the study will be to compare the effect of Egoscue versus Pilates exercises on pain, range of motion and muscle endurance in patient with mechanical low back pain.

NCT ID: NCT06446596 Not yet recruiting - Low Back Pain Clinical Trials

TRAK vs Standard Home-based Exercise in Low Back Pain

Start date: June 2024
Phase: N/A
Study type: Interventional

The objective of the study is to compare the effect of a home therapeutic exercise intervention scheduled through the application of digital physiotherapy and telerehabilitation TRAK, versus a home therapeutic exercise program scheduled through a dossier and an exercise diary, with respect to disability (measured using the OSWESTRY questionnaire) and other variables (range of motion, strength, fatigue, histological changes, pain, medication intake, psychosocial factors and adherence), in patients with low back pain.

NCT ID: NCT06437314 Not yet recruiting - Healthy Clinical Trials

Effect of an Intervention Based on Back School in an Aquatic Environment on Non-specific Low Back Pain

Start date: July 10, 2024
Phase: N/A
Study type: Interventional

A controlled and randomized clinical trial will be conducted, in which scores on dependent variable measures will be compared before and after the intervention, both in the experimental group (EG) (individuals who will attend the in an aquatic program based on the back school) and in the control group (CG) (individuals who will not attend the in an aquatic program based on the back school). The experimental procedure will follow the recommendations of the CONSORT and TidIER guidelines. The study protocol will be approved by the Research Ethics Committee of the University of Vigo. This study will be conducted under the Declaration of Helsinki (2013 version). Participants will sign a written informed consent after being informed of the benefits and risks of the research. Participants in the EG will participate in an aquatic program based on the back school. This program will follow the recommendations of the biopsychosocial model of chronic pain and will be conducted in an aquatic environment. The intervention will be carried out by physiotherapists in a sports centre. The duration of the intervention will be six weeks, with a frequency of two sessions per week, totalling 12 sessions of 45 minutes each. Of all the sessions, 10 will have a practical focus and the other two will have a theoretical focus.

NCT ID: NCT06430255 Not yet recruiting - Pain, Back Clinical Trials

Effects of Global Postural Re-education Versus Laser-guided Exercise in Non-specific Chronic Low Back Pain

Start date: May 16, 2024
Phase: N/A
Study type: Interventional

Effects of Global Postural Re-education Versus Laser-guided Supervised Exercise in Individuals With Non-specific Chronic Low Back Pain

NCT ID: NCT06427434 Not yet recruiting - Low Back Pain Clinical Trials

Effect of Modified Lumbar Sustained Natural Apophyseal Glide on Postnatal Low Back Pain

Start date: May 30, 2024
Phase: N/A
Study type: Interventional

This study will be carried out to evaluate the effect of modified lumbar Sustained Natural Apophyseal Glide on low back pain in postnatal women.

NCT ID: NCT06420596 Not yet recruiting - Low Back Pain Clinical Trials

The Effectiveness of Remote App-assisted Physiotherapy in Patients With Non-specific Low Back Pain (RemotePT)

Start date: May 2024
Phase: N/A
Study type: Interventional

The aim of this single-center, observational randomised controlled trial is to evaluate the effectiveness of using Akina Cloud, a remote app-assisted physiotherapy, in managing non-specific low back pain among patients.

NCT ID: NCT06419439 Not yet recruiting - Depression Clinical Trials

Ketamine-assisted Integrative Treatment for Veterans With Chronic Low Back Pain and Comorbid Depression

Start date: December 1, 2025
Phase: Phase 2
Study type: Interventional

This is a pilot study to evaluate the feasibility, acceptability, and safety of ketamine infusions followed by a brief behavioral intervention in Veterans with chronic low back pain and depression.

NCT ID: NCT06410027 Not yet recruiting - Clinical trials for Chronic Low-back Pain

Effects of Pain Neuroscience Education and Virtual Reality in Patients With Chronic Low Back Pain

Start date: May 8, 2024
Phase: N/A
Study type: Interventional

The objective of our study is to evaluate the effects of a therapeutic intervention including 1-hour of pain neuroscience education session, 30-minutes of exposure to exercise with virtual realit and therapeutic exercise in patients with chronic low back pain.

NCT ID: NCT06404788 Not yet recruiting - Chronic Pain Clinical Trials

Anxiety Level Among Patients With Chronic Low Back Pain

Start date: May 6, 2024
Phase:
Study type: Observational

The goal of this observational cross-sectional study is to learn about the intensity of anxiety symptoms among Polish people suffering from chronic lower back pain. The main question it aims to answer is: What is the severity of anxiety symptoms among the Polish population of patients suffering from chronic lower back pain?

NCT ID: NCT06399497 Not yet recruiting - Low Back Pain Clinical Trials

Effects of Lumbar Spinal Manipulation in Subjects With Chronic Low Back Pain

LBP-HVLA
Start date: May 2024
Phase: N/A
Study type: Interventional

This study aims to measure the effects of spinal manipulation on Chronic Spinal Pain by assessing Muscle Mechanical Properties (MMPs) using MyotonPRO®, Mechanical Perception Threshold (MPT) using Von Frey monofilaments, and Pressure Pain Threshold (PPT) using an algometer. Participants will be randomly assigned to either spinal manipulation or placebo groups to compare effects on MMPs, MPT, and PPT. Assessments will occur at three time points: baseline, immediately post-intervention (real or simulated), and 24 hours post-intervention. This research targets individuals with chronic spinal pain, providing insights into the potential benefits of spinal manipulation in managing this condition.