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Educational Program for Knee Osteoarthritis

F

Federal University of São Paulo

Status

Completed

Conditions

Knee Osteoarthritis

Treatments

Device: Transcutaneous Nerve Electro-Stimulation
Other: Educational Program

Study type

Interventional

Funder types

Other

Identifiers

NCT03588195
CEP UNIFESP 458293

Details and patient eligibility

About

Sixty patients with a diagnosis of knee osteoarthritis, aged between 40 and 80 years, of both genders were included. The patients were divided into: experimental group that carried out an educational program - 5 consecutive sessions held once a week, with a duration of 60 minutes each class and at the end of the last class, a booklet was delivered for each patient with all the contents of the classes and the Transcutaneous Nerve Electro-Stimulation device - being performed twice weekly, for 5 weeks for 40 minutes each session; and control group who only underwent treatment with the Transcutaneous Nerve Electro-Stimulation in the same parameters as experimental group. The evaluations were performed at the beginning of the treatment, 4 and 12 weeks after the beginning of the treatment using a numerical pain scale; WOMAC; IDATE and SF-36 questionnaires; and 6-minute walk test.

Enrollment

60 patients

Sex

All

Ages

40 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of knee Osteoarthritis by American College of Rheumatology criteria;
  • Age between 40 and 80 years;
  • Both genders;
  • Numerical Pain Scale in the knee between 3 and 8 centimeters on a scale of 0 to 10 centimeters.

Exclusion criteria

  • Systemic inflammatory diseases or any condition that prevents the practice of physical activity;
  • Regular physical activity started or changed in the last twelve weeks;
  • No ambulation;
  • Joint injection in the knee in the previous twelve weeks;
  • Previous knee surgery or surgery planned for the next twenty-four weeks;
  • Physiotherapy in the last twelve weeks;
  • Other disease that affects the lower limbs;
  • Open wounds at the electrode application site;
  • Planned trip in the next twelve weeks.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Education Group
Experimental group
Treatment:
Device: Transcutaneous Nerve Electro-Stimulation
Other: Educational Program
Control Group
Active Comparator group
Treatment:
Device: Transcutaneous Nerve Electro-Stimulation

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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