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Back Pain clinical trials

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NCT ID: NCT06428565 Active, not recruiting - Low Back Pain Clinical Trials

Conventional Exercises Plan With or Without Laser Guided Feedback for Patients With Non-Specific Low Back Pain

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

Low back pain (LBP) is a significant health issue. It impacts a significant portion of the adult population, reaching up to 80%, and results in substantial healthcare and socioeconomic expenses. To find out what changes occurred after the application of two exercise modalities [Conventional Exercise (CE) and Laser-Guided Exercise (LGE)} and PNE on pain, pain pressure thresholds, disability, catastrophizing, kinesiophobia, and lumbar proprioception in subjects with NSCLBP.

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: NCT06425744 Completed - Low Back Pain Clinical Trials

Impact of Pilates and Myofascial Release on Women's Chronic Low Back Pain

Start date: August 8, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to find out if Reformer Pilates and self-myofascial release are effective for pain and muscle function in women with chronic low back pain. Investigators will also look at changes in quality of life. The main questions for the study are Can Reformer Pilates and self-myofascial release reduce pain in participants? Can Reformer Pilates and self-myofascial release change muscle function in participants? The researchers want to compare the effects of Reformer Pilates and self-myofascial release in women with chronic low back pain. Participants will be Group 1 Perform Reformer Pilates and self-myofascial release exercises twice a week for 6 weeks, for a total of 12 sessions. Group 2 Perform Reformer Pilates exercises twice a week for 6 weeks, for a total of 12 sessions. Participants will visit the Pilates Centre for an examination before and once after starting the programme. All groups perform a home exercise training programme for 15 minutes three times a week.

NCT ID: NCT06423755 Completed - Clinical trials for Chronic Low-back Pain

Swimming Versus Standard Physiotherapy Care as Rehabilitation Modalities for Persistent Low Back Pain: Feasibility Study

Start date: September 1, 2021
Phase: N/A
Study type: Interventional

Study four: A small scale RCT will be conducted to pilot the swimming lessons developed in study three, to compare the lessons to standard physiotherapy care and to assess the feasibility of conducting a large RCT in the future. The results from this feasibility study will give the researcher some initial feedback on the swimming lessons and will inform and support the development of an RCT in the future; if the initial findings are positive. This will include whether an RCT can be carried out and evaluating recruitment and retention rates, willingness to be randomised, adverse events, outcomes, acceptability and cost analysis.

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: NCT06417255 Recruiting - Clinical trials for Low Back Pain, Mechanical

Comparison Of The Effects Of Kinesiotape Application And Foam Roller Exercises

Start date: May 11, 2024
Phase: N/A
Study type: Interventional

Low back pain is an important health problem that is common worldwide, with a lifetime prevalence of up to 80%.

NCT ID: NCT06415825 Not yet recruiting - Arthropathy of Knee Clinical Trials

Preliminary Muscle Contraction in the Rehabilitation and Prevention of Degenerative Pain in the Locomotor System

PMQRPDP
Start date: May 14, 2024
Phase: N/A
Study type: Interventional

RESEARCH OBJECTIVE: To investigate the effect of muscle preliminary contraction in the rehabilitation and prevention of degenerative pain in the spine, hip, knee, ankle, shoulder, elbow, and ankle joints, as well as after hip and knee arthroplasty. HYPOTHESIS: Muscle preliminary contraction has a significant short-term and long-term effect in the rehabilitation and prevention of degenerative pain in the spine, hip, knee, ankle, shoulder, elbow, and ankle joints, as well as after hip and knee arthroplasty. RESEARCH METHODS: At least 216 patients with degenerative pain in the spine, hip, knee, ankle, shoulder, elbow, and ankle joints, as well as after hip and knee arthroplasty, will be studied. They will be randomized into pairwise sub-groups. All will receive standard advice. The maneuver sub¬groups will receive additional advice - preliminary contraction of the muscles in the corresponding kinesiology segment. This advice will be embedded in all motor activities of daily living involving the relevant area. The following follow-up parameters will be used: visual analogue pain scale, manual muscle testing, goniometry, centimeter, and preliminary contraction success rate. Their follow-up will be threefold - at the beginning, after 1, and after 6 months. For statistical processing, multiple analysis of variance (MANOVA), with post hoc Bonferroni multiple tests, and Pearson correlation analysis, with post hoc regression analysis, will be used. CONCLUSION: The positive results will allow the preliminary muscle contraction to be used as a universal tool in the rehabilitation, prevention, and prevention of degenerative pain in the spine, hip, knee, ankle, shoulder, elbow, and ankle joints, as well as after hip and knee arthroplasty (international contribution). This maneuver is very short (seconds), easy (everybody can perform it), does not require the allocation of time, space, and resources (including financial ones), and is instantly incorporated into everyday life.

NCT ID: NCT06415461 Recruiting - Pain, Back Clinical Trials

Open Label Dose Ranging Study Assessing the Safety of Cord Blood Product in Sacroiliac Joint Syndrome (SIJ)

SIJ
Start date: May 10, 2024
Phase: Phase 1
Study type: Interventional

This is a Phase 1 trial. The overall objective is to evaluate the safety and potential efficacy effect of specific type of umbilical cord blood product (CFL001), which, other than specific modifications in manufacturing to render it compatible with cGMP, is essentially similar to that reported in real-world experience.

NCT ID: NCT06412484 Recruiting - Low Back Pain Clinical Trials

State vs. Trait Alterations in Low Back Pain

Start date: October 1, 2023
Phase:
Study type: Observational

The primary goal of this study is to investigate whether different alterations observed in patients with non-specific episodic low back pain (compared to healthy volunteers), detected using several assessments: psychophysical and neurophysiological testing, imaging, and blood sampling, are dependent or independent of the presence and type of pain experienced at the time of investigation.