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Progressive Collective-exercise Program on the Knee Osteoarthritis

Not Applicable
Completed
Conditions
Knee Osteoarthritis
Interventions
Other: Collective group exercise program in patients with KOA
Other: Orientation (without exercise)
Registration Number
NCT01850862
Lead Sponsor
Universidade Federal do Rio Grande do Norte
Brief Summary

The investigators hypothesized that an eight-week collective group exercise program would improve pain, quality of life and functional capacity in patients with knee osteoarthritis (KOA) compared with those receiving no exercise intervention.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
30
Inclusion Criteria
  • symptomatic and moderate to severe medical diagnostic of KOA.
  • Subjects with normal cognitive functions and no restriction to perform physical activities were recruited from the hospital's KOA database and eligible to participate if they had presented: Lequesne questionnaire criteria (5 - 13.5), knee pain score between 3 and 7 (on a 0 -10 Visual Analogue Scale), stable doses of non-steroidal anti-inflammatory drugs (NSAIDs) and no regular physical exercise or use of canes in the months prior to the study.
Exclusion Criteria
  • Symptomatic heart disease; symptomatic disease of the lower limbs (other than KOA); symptomatic lung disease; severe systemic disease; severe psychiatric illness; regular physical exercise (three or more times per week for at least 3 months); drug injection in the knee in the previous 3 months; physiotherapy on the lower limbs in the previous 3 months and absence in two consecutive training sessions or three nonconsecutive sessions

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Collective group exercise program in patients with KOACollective group exercise program in patients with KOACollective exercises program for patients with osteoarthritis and orientation about this disease
Control group (without exercise)Orientation (without exercise)Orientation about osteoarthritis disease but without any exercise program
Primary Outcome Measures
NameTimeMethod
PainEight weeks

pain assessed by Visual Analogue Scale

Secondary Outcome Measures
NameTimeMethod
quality of lifeEight weeks

quality of life assessed by SF-36 questionnaire

Trial Locations

Locations (1)

Federal University of Rio Grande do Norte

🇧🇷

Natal, RN, Brazil

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