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Fascial Manipulation in Patients With Hip Osteoarthritis

NCT ID: NCT02305108

Last Updated: 2015-11-20

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

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-06-30

Study Completion Date

2015-06-30

Brief Summary

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The study will test the efficacy of the treatment of soft tissues for osteoarthritis patients that are waiting for total hip arthroplasty. The fascial manipulation provides a deep pressure of specific points of the muscle fascia. The aims of this treatment are the improve of pain before the surgery and the improve of functional performance after the surgery.

Detailed Description

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Conditions

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Osteoarthritis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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fascial manipolation and standard

Group Type EXPERIMENTAL

fascial manipulation

Intervention Type OTHER

Recruited patients in study's group will be treated with the standard treatment and fascial manipulation.

Specific points of fascial tissue will be treated with a deep friction to improve elasticity.

The number of point treated will be refered to a specific evaluation for each patient.

Fascial manipulation provide 3 session treatment (one treatment for week).

standard treatment

Intervention Type OTHER

Before surgery, standard physiotherapy treatment provides an education session about the rehabilitation program tha is going to be execute after surgery.

After surgery 2 daily physiotherapy treatment are implemented: bed exercise as active and passive flex-extension of lower limb, movements for postural change to reach sitting and standing position, walking training.

standard treatment

Group Type ACTIVE_COMPARATOR

standard treatment

Intervention Type OTHER

Before surgery, standard physiotherapy treatment provides an education session about the rehabilitation program tha is going to be execute after surgery.

After surgery 2 daily physiotherapy treatment are implemented: bed exercise as active and passive flex-extension of lower limb, movements for postural change to reach sitting and standing position, walking training.

Interventions

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fascial manipulation

Recruited patients in study's group will be treated with the standard treatment and fascial manipulation.

Specific points of fascial tissue will be treated with a deep friction to improve elasticity.

The number of point treated will be refered to a specific evaluation for each patient.

Fascial manipulation provide 3 session treatment (one treatment for week).

Intervention Type OTHER

standard treatment

Before surgery, standard physiotherapy treatment provides an education session about the rehabilitation program tha is going to be execute after surgery.

After surgery 2 daily physiotherapy treatment are implemented: bed exercise as active and passive flex-extension of lower limb, movements for postural change to reach sitting and standing position, walking training.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* patients age 40-80, with primary coxarthrosis waiting for total hip arthroplasty that complain a pain measured by Numeric Rating Scale ≥ 5 and that live in Bologna

Exclusion Criteria

* arthroplasty revision or substitution. Patient with cognitive deficiency and severe comorbidity (rheumatic, neurological or cardiovascular pathology)
Minimum Eligible Age

40 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Istituto Ortopedico Rizzoli

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Andrea Cotti, PT

Role: PRINCIPAL_INVESTIGATOR

Istituto Ortopedico Rizzoli

Locations

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Istituto Ortopedico Rizzoli

Bologna, Bo, Italy

Site Status

Countries

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Italy

Other Identifiers

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Prot. gen. 0018810

Identifier Type: -

Identifier Source: org_study_id