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

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-02-28

Study Completion Date

2016-10-31

Brief Summary

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Introduction: Lower extremity weakness associated with musculoskeletal pathology can cause activity limitations. Physical therapy intervention in the form of exercise is commonly directed at improving muscular performance, however, neuromuscular adaptations may limit the effectiveness of traditional strengthening exercises. Manual therapy techniques have been used as a disinhibitory intervention to increase muscle activation and strength before participating in strengthening exercises or performing functional tasks While there is recent evidence to support joint mobilization as a valuable manual therapy disinhibitory intervention Currently, there is no evidence to substantiate anecdotal experience that a HVLAT hip distraction mobilization improves muscle performance in subjects with lower extremity pathology and lower extremity weakness. The purpose of this study was to determine if a HVLAT hip distraction mobilization would result in an immediate change of maximal force output of the quadriceps, gluteus maximus and gluteus medius.

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.

Detailed Description

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Conditions

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Hip Joint Muscle Weakness

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Investigators

Study Groups

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Placebo Group

Hip manipulation simulation

Group Type PLACEBO_COMPARATOR

Hip manipulation simulation

Intervention Type OTHER

Hip manipulation simulation

Manipulation Group

Hip manipulation

Group Type EXPERIMENTAL

Hip mobilization

Intervention Type OTHER

High velocity low amplitude hip mobilization of the experimental group

Interventions

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Hip mobilization

High velocity low amplitude hip mobilization of the experimental group

Intervention Type OTHER

Hip manipulation simulation

Hip manipulation simulation

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Individuals with a lower extremity pathology volunteered for this study
* 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

* Included individuals with a history lower extremity arthroplasty.
* 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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Faculdade de Ciências Médicas da Santa Casa de São Paulo

OTHER

Sponsor Role lead

Responsible Party

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Diego Galace de Freitas

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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DFreitas

Identifier Type: -

Identifier Source: org_study_id

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