Vibration

6

Review clinical trials related to Vibration. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Effect of Dry Needling Plus Vibration on Myofascial Trigger Points in Individuals With Nonspecific Low Back Pain

This study evaluates whether adding mechanical vibration to dry needling (DN+V) is not inferior to dry needling alone (DN) for reducing low back pain intensity in adults with nonspecific low back pain (NSLBP), when both interventions are combined with a structured exercise program. The primary hypothesis is non-inferiority in pain reduction (Numeric Pain Rating Scale, NPRS) at 1 week after treatment, using a non-inferiority margin of 1 point on the 0-10 NPRS scale. If non-inferiority is confirmed, secondary analyses will explore whether DN+V is superior to DN alone in patient-reported treatment acceptability, pain experienced during the intervention, and post-needling soreness. Participants will be randomly assigned to one of two parallel groups: DN plus exercise, or DN+V plus exercise. Outcomes will be assessed at baseline and at multiple time points up to 4 weeks after treatment, including pain intensity, disability, acceptability, muscle strength, pressure pain threshold, quality of life, and global impression of change. Direct and indirect costs associated with both interventions will also be collected to provide data for a future economic evaluation of the cost-effectiveness of DN+V compared with DN.

Participants needed: 108
Trial details
Age: 35-65Biological sex: AllType: InterventionalSponsor: Universidad de ZaragozaUpdated: Oct 5, 2026Locations: 2
Eligibility criteria

Individuals with NSLBP: pain persisting for more than six weeks, located between... [+3]

Diagnosis of specific pathologies associated with low back pain (e.g., herniated... [+7]

Status: Recruiting

Effect of Vibration and ShotBlocker on Pain and Fear Levels During Intramuscular Injection in Children in the Emergency Department

This prospective study is planned as a randomized controlled study. The aim of this study is to investigate the effects of vibration and the ShotBlocker method on pain and fear levels in children during intramuscular injection in the emergency department.

Participants needed: 120
Trial details
Age: 5-10Biological sex: AllType: InterventionalSponsor: Burdur Mehmet Akif Ersoy UniversityUpdated: Aug 6, 2026Locations: 1
Eligibility criteria

Volunteering of the child and parent to participate in the study, [+2]

Communication problem, [+2]

Status: Recruiting

The Course of Acute Respiratory Failure in Geriatric Patients With Hip Fracture Using Different Modes of a Vibroacoustic Device for the Lungs

A medical professional trained in the procedure and use of the device will conduct the vibroacoustic therapy session. He will also take blood samples. In the control group, patients will undergo vibroacoustic pulmonary therapy in the "Pneumonia" mode, and in the control group, in the "Prevention" mode. Vibroacoustic pulmonary therapy will be conducted over a period of 5 days. A similar algorithm of actions is planned for both groups. VALT sessions will be conducted 4-6 times a day for 5 minutes in combination with treatment according to the protocol for the use of "Vibroacoustic Therapy" of the lungs of the Ministry of Health of the Republic of Kazakhstan. The device's emitters will be applied to the affected areas of the lungs. Since the device has long cords for the emitters and is portable, it is not difficult to change the patient's position and does not require their active participation, which is important for patients on ventilators and with limited mobility.

Participants needed: 60
Trial details
Age: 60-85Biological sex: AllType: InterventionalSponsor: Astana Medical UniversityUpdated: Apr 8, 2026Locations: 1
Eligibility criteria

respiratory failure; [+2]

terminal condition of the patient; [+15]

Status: Recruiting

IASTM and Vibration Effects on Pain, Functionality, and Kinesiophobia in Lumbar Disc Herniation

The aim of this study is to investigate the effects of Instrument-Assisted Soft Tissue Mobilization and vibration massage therapy on pain, functionality, and kinesiophobia in individuals with lumbar disc herniation.

Participants needed: 45
Trial details
Age: 30-60Biological sex: AllType: InterventionalSponsor: Istanbul Medipol University HospitalUpdated: Mar 27, 2026Locations: 1
Eligibility criteria

Individuals between 30 and 60 years of age [+4]

Individuals with a history of lumbar surgery [+6]

Status: Recruiting

Non-invasive Vibratory Stimulation of the Knee Muscles for the Improvement of the Somatosensory Input and Motor Performance

The goal of this interventional cross-sectional study is to evaluate motor responses to non-invasive vibratory stimulation applied to the hamstring muscle tendons in healthy individuals. Knee flexion and extension efforts, in both isometric and concentric contractions, will be tested. The investigators hypothesize that vibratory stimulation causes an increase in activity in the flexor muscles (hamstrings) and a decrease in the extensor muscles (quadriceps) of the knee in all motor tasks. It follows that during knee flexion (both concentric and isometric), vibratory stimulation should cause an increase in the distance between the angular trajectories of the knee obtained with and without vibratory stimulation (with a positive sign). The increased activity of the hamstring muscles would, in fact, contribute to increasing the velocity of the flexor movement. Conversely, during extensor movements (both concentric and isometric), vibratory stimulation should reduce the instantaneous velocity of the movement, therefore causing an increase in distance (with a negative sign) between the trajectories obtained with and without stimulation. Participants will be tested using an isokinetic dynamometer and they will be asked to perform the following motor tasks in a random order: concentric knee flexion, concentric knee extension, isometric knee flexion, and isometric knee extension. The dominant limb will be tested, only. The assessment will be performed one time.

Participants needed: 35
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of Milano BicoccaUpdated: Feb 20, 2026Locations: 1
Eligibility criteria

Age equal to or greater than 18 years.

Neurological disorders. [+2]

Status: Not yet recruiting

Sensory Mechanisms of Manual Dexterity Recovery After Stroke: a Prospective Cohort Study of Prediction and Cerebral Correlates

In the proposed research, we will assess motor and sensory functions of the hand using clinical tests and a tool designed to measure manual dexterity combined with vibrotactile stimulation. We will also evaluate the integrity of brain structure and function using MRI.

Participants needed: 90
Trial details
Age: 18-85Biological sex: AllType: InterventionalSponsor: Centre Hospitalier St AnneUpdated: Jan 14, 2026Locations: 1
Eligibility criteria

First symptomatic stroke, ischaemic or haemorrhagic in the early subacute phase... [+3]

Presence of another neurological or musculoskeletal condition affecting upper li... [+8]