Progressive Collective-exercise Program on the Knee Osteoarthritis
Not Applicable
Completed
- Conditions
- Knee Osteoarthritis
- Interventions
- Other: Collective group exercise program in patients with KOAOther: 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
Group Intervention Description Collective group exercise program in patients with KOA Collective group exercise program in patients with KOA Collective 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
Name Time Method Pain Eight weeks pain assessed by Visual Analogue Scale
- Secondary Outcome Measures
Name Time Method quality of life Eight weeks quality of life assessed by SF-36 questionnaire
Trial Locations
- Locations (1)
Federal University of Rio Grande do Norte
🇧🇷Natal, RN, Brazil