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Completed

NCT Number: NCT02919020

Efficacy of Proprioceptive Neuromuscular Facilitation in Older Women With Gonarthrosis

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.

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Key information

Age range

50 year–80 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Hospital Universitário Drº Washigton Antônio de Barros

Petrolina, Pernambuco, 50710430, Brazil

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women;
  • 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 ) .

Treatment and study plan

Proprioceptive neuromuscular facilitation (PNF)

Other

Proprioceptive neuromuscular facilitation, using the technique of rhythmic initiation and Combination of Isotonic on lower members

Resistance Exercise

Other

resistance exercise to strengthen lower limbs

Primary outcomes

  1. Change in pain

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

    "Pain control diary"

  2. Quality of life

    Time frame: change from baseline in quality of life 6th-12th week

    Western Ontario and McMaster Universities Questionaire

  3. Functional performance

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

    "30 s -chair stand test"

  4. Quality of life

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

    Medical Outcomes Study 36 - Item Short - Form Health Survey

  5. Functional Performance

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

    "Walk Test of 40 meters at a rapid pace

  6. Functional Performance

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

    "Stair climb test"

Secondary outcomes

  1. pain sensitivity threshold

    Time frame: change from baseline in pain threshold 6th-12th week pressure

    "Algometry"

  2. Range of motion

    Time frame: "change from baseline in the range of knee flexion 6th-12th week"

    "Universal Goniometer"

Sponsors and collaborators

Lead sponsor

Universidade Federal de Pernambuco

Other

Collaborators

  • Angélica da Silva Tenório
  • Daniella Araújo de Oliveira

Registry information

Official study title

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

Acronym: PNF

Important dates

Study start
2017
Primary completion
2018
Study completion
2019
First posted
Sep 29, 2016
Registry last updated
Jul 22, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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