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Clinical Trials/NCT02919020
NCT02919020
Completed
Not Applicable

Efficacy of Proprioceptive Neuromuscular Facilitation About Functional Performance, Pain and Quality of Life in Older Women With Gonarthrosis: Randomized Controlled Trial

Universidade Federal de Pernambuco1 site in 1 country15 target enrollmentJanuary 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Osteoarthritis Knee
Sponsor
Universidade Federal de Pernambuco
Enrollment
15
Locations
1
Primary Endpoint
Change in pain
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

To evaluate the effectiveness of the method Proprioceptive Neuromuscular Facilitation (PNF) as physical therapy approach to the reduction of pain and improvement in functional performance and quality of life in women with knee osteoarthritis.

Detailed Description

Patients will be divided into two groups: group perform proprioceptive neuromuscular facilitation and other group submit performing resistance exercises.

Registry
clinicaltrials.gov
Start Date
January 2017
End Date
February 2019
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Thaís Ferreira Lopes Diniz Maia

Investigador Principal

Universidade Federal de Pernambuco

Eligibility Criteria

Inclusion Criteria

  • Age between 50 and 80 years;
  • Clinical diagnosis of Osteoarthritis of knees ;
  • Patients with presence of at least 90 ° range of motion of knee flexion ;
  • Do not practitioners of physical exercise and physical therapy during the period of participation in the survey

Exclusion Criteria

  • Diagnosis of other rheumatological and neurological diseases ;
  • orthopedic surgery History in the lower limbs ;
  • Individuals with muscle strength of the lower limbs \<3 ;
  • Cognitive impairment or neurological disease that compromises the understanding and implementation of the Protocol (Mini Mental State Examination \<18 for the illiterate and \<24 for others);
  • Body mass index ≥ 30.0 (obesity , according to the World Health Organization ) .
  • Individuals classified as physical activity level "very active" by the IPAQ (International Physical Activity Questionnaire ) .

Outcomes

Primary Outcomes

Change in pain

Time Frame: "change from baseline in pain 6th - 12th week"

"Pain control diary"

Quality of life

Time Frame: Change based on functional performance 6th - 12th week

Medical Outcomes Study 36 - Item Short - Form Health Survey

Functional performance

Time Frame: Change based on functional performance 6th - 12th week

"30 s -chair stand test"

Functional Performance

Time Frame: "Walk Test of 40 meters at a rapid pace

"Stair climb test"

Secondary Outcomes

  • Range of motion("change from baseline in the range of knee flexion 6th-12th week")
  • pain sensitivity threshold(change from baseline in pain threshold 6th-12th week pressure)

Study Sites (1)

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