The Effect High Velocity Low Amplitude Hip Mobilization on Strength in Subjects With Lower Extremity Pathology
NCT ID: NCT03115879
Last Updated: 2017-04-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
40 participants
INTERVENTIONAL
2015-02-28
2016-10-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Methods: Forty individuals with a lower extremity pathology volunteered for this study. Inclusion criteria were having a unilateral musculoskeletal pathology, being greater than 18 years of age, 10% decrease in muscle strength in symptomatic side compared to healthy side, and absence of medical precautions that would prevent a maximal effort strength test and exclusion criteria included individuals with a history lower extremity recent muscle or tendon ruptures (within the past 6 months) and postoperative knee, hip and ankle surgery. Demographic data, including diagnosis from referring physician were collected. All subjects completed the Lower extremity function scale (LEFS). A single evaluator blinded to the involved extremity was responsible for quadriceps, gluteus medius and maximus strength analysis pre and post mobilization of both symptomatic and non-symptomatic sides. The subject underwent the HVLAT hip distraction mobilization of the symptomatic side, and an immediate re-assessment of strength of both symptomatic and non-symptomatic sides followed the mobilization.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Hip Manipulation for Improved Strength in Patients With Hip Pain
NCT06655987
Utilizing the Trunk as a Proximal Lever to Strengthen the Hip Musculature and Alter Lower Extremity Function
NCT03285464
Hip Abductor Strengthening With Proprioceptive Neuromuscular Facilitation
NCT05840523
Comparing the Effects of Mobilization With Movement (MWM), Self MWM, and Dynamic Stretching on Hip Internal Rotation)
NCT04279756
Vascular Occlusion in Patients With Osteoarthritis
NCT01483131
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Placebo Group
Hip manipulation simulation
Hip manipulation simulation
Hip manipulation simulation
Manipulation Group
Hip manipulation
Hip mobilization
High velocity low amplitude hip mobilization of the experimental group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Hip mobilization
High velocity low amplitude hip mobilization of the experimental group
Hip manipulation simulation
Hip manipulation simulation
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Being greater than 18 years of age
* 10% decrease in muscle strength in symptomatic side compared to healthy side
* Absence of medical precautions that would prevent a maximal effort strength test.
Exclusion Criteria
* Recent muscle or tendon ruptures (within the past 6 months)
* Unhealed fractures
* Neurological diseases
* Malignant cancer
* Osteoporosis
* Active infections processes
* Early postoperative knee, hip and ankle surgery with range of motion and weight bearing restrictions.
18 Years
50 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Faculdade de Ciências Médicas da Santa Casa de São Paulo
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Diego Galace de Freitas
Principal Investigator
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
DFreitas
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.