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Effects of a water-based Exercise Program in elderly women with Knee Osteoarthritis

Comparison of the effects of an Exercise Program performed in water or land in elderly with Hip or Knee Osteoarthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-7zcgdd
Enrollment
Unknown
Registered
2018-07-04
Start date
2015-02-10
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Knee osteoarthritis

Interventions

Experimental group: A single group of 22 elderly women with knee osteoarthritis underwent an evaluation phase followed by a four-week control period maintaining their usual activities before the inte
Other
G11.427.410.698.277

Sponsors

Departamento de Educação Física da Universidade Federal do Paraná
Lead Sponsor
Centro Universitário Unibrasil
Collaborator

Eligibility

Sex/Gender
Female
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: Women; age from 60 years; diagnosed with knee osteoarthritis by a physician; able to walk with no help of assistive device; able to practice exercise.

Exclusion criteria

Exclusion criteria: Elderly women with diagnosed osteoarthritis or prosthesis in other lower limb joint; with medical restrictions to physical activity; participating on exercise program in last six months; with ortopaedic surgery in last six months.

Design outcomes

Primary

MeasureTime frame
Expected outcome 1: Knee estensor and flexor muscle strength and power enhancement, measured through isokinetic knee extension and flexion strength test using an isokinetic dynamometer at angular velocities of 60°/s and 180°/s, from at least 15% variation between pre and post intervention measures. ;Observed outcome 1: After the exercise program there was an increase of 24,1% in total work of knee flexor muscles; 16,8% in knee flexor muscles peak torque; 15,6% increase in knee extensor muscle power; and 26,8% increase in knee flexor muscle power.;Expected outcome 2: Enhancement in physical function, represented by increased usual gait speed measured in a linear 4-meter course; decreased time to perform five times Sit-to-Stand Test; increased distance in the 6minute Walking Test, performed in a linear 30 meter course; decreased time to perform the Timed Up and Go Test; increased gait speed measured through 10-meter Walking Test in maximum velocity, from at least 5% variation between pre and post intervention measures. ;Observed oucome 2: After the intervention was observed 10,1% reduction on time to perform the sit-to-stand test; 9,2% reduction on time to perform the TUG test; and 13,2% on covered distance in 6 minute walking test. There were no changes in gait speed on 4m and 10m walking tests.;Expected outcome 3: Reduction in KOA symptoms of pain, joint stiffness and functional limitations, measured through Western Ontario and McMaster Universities Index (WOMAC), from at least 10% variation between pre and post intervention measures. ;Observed outcome 3: Reduction of 22% in joint stiffness; 12% enhancement in physical function; and 15% on WOMAC total score.

Secondary

MeasureTime frame
Expected outcome 1: Perceived pain measured through a visual analog scale, from at least 50% variation between pre and post intervention measures.;Observed outcome 1: Perceived knee pain reduction of 75%.;Expected outcome 2: Decreased postural sway measured through static balance test in a force plate, from 10% variation in pre and post intervention measures.;Observed outcome 2: there were no changes in postural sway after the intervention.;Expected outcome 3: Enhancement on usual gait spatial and temporal paramenter, measured through kinetic and kinematic gait evaluation, using a camera system, a force plate and an image processing software, from 5% variation in observed parameters between pre and post intervention measures. ;Observed outcome 3: There were no changes in usual gait spatial and temporal parameters after the intervention.

Countries

Brazil

Contacts

Public ContactPaulo Barauce Bento

Universidade Federal do Paraná

ferdymattos@hotmail.com+55 41 33604333

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 18, 2026