Skip to content

Effect of low-level laser and exercise improving balance and functionality in people with knee osteoarthritis

Effect of Low-level Laser Therapy associated or not to exercise in subjects with knee osteoarthritis: randomized study on the impact of physical therapy clinical trial on postural control and functionality

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-7s6ymc
Enrollment
Unknown
Registered
2015-07-28
Start date
2015-08-01
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

osteoarthritis

Interventions

Participants will be divided into five groups: 1) Control group without OA group (n = 15): subjects without OA and no treatment. 2) Control group with OA group (n = 15): patients with osteoarthritis a
2) Strengthening exercises for the lower limbs (20 minutes)
3) Aerobic exercise (exercise bike) (20 minutes)
4) Stretching (5 minutes). Laser + exercise: Participants randomized to this group will carry out the exercise program (50 minutes) followed by the application of low power laser (56 seconds per point
Other
G11.427.590.530.698.277
E02.779.483
E02.779.483.875
E02.594

Sponsors

Faculdade de Medicina de Ribeirão Preto - Universidade de São Paulo
Lead Sponsor
Faculdade de Medicina de Ribeirão Preto - Universidade de São Paulo
Collaborator

Eligibility

Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: Individuals of both genders, with ages between 40 and 70 years, with or without knee osteoarthritis.

Exclusion criteria

Exclusion criteria: Cardiovascular disease; neurological or musculoskeletal that disables the volunteer to perform exercises; evidence of secondary disease, inflammatory or metabolic; osteonecrosis and previous intra-articular injection; surgery in the previous three months to inclusion in the study or use of drug treatment that could potentially have an effect on the results of study.

Design outcomes

Primary

MeasureTime frame
Improvement of average of velocity of gait in centimeters per second; that will assessed by equipment: Gaitrite Platinum 26 'Portable Walkway System; expected an increase of at least 10% of the average of speed of gait evaluated by the equipment: gaitrite Platinum pre and post-intervention.

Secondary

MeasureTime frame
Improvement of pain, i.e., decreasing Womac questionnaire scores, improved posture control (reduction sway of the center pressure) and the force (in Newtons / meter) and muscle strength (measured in Watts) to be evaluated by questionnaire Womac by Balance Master System and the Biodex isokinetic respectively. It is expected that there is a change of classification of the questionnaire Womac pre and post-intervention, which occurs a decrease of the oscillation center of pressure of at least 10% (improvement in postural control) measured by Master balance and increased strength and muscular strength of at least 10% pre- and post-intervention.

Countries

Brazil

Contacts

Public ContactDaniela;Daniela Abreu;Abreu

Faculdade de Medicina de Ribeirão Preto - Universidade de São Paulo;Faculdade de Medicina de Ribeirão Preto - USP

dabreu@fmrp.usp.br;dabreu@fmrp.usp.br+55 (16) 3602 3176 ;+55 (16) 6302 3176

Outcome results

None listed

Source: REBEC (via WHO ICTRP)