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Improvement of quality of life after knee prosthesis

Evaluation of quality of life improvement after total knee artrhroplaty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-588cfq
Enrollment
Unknown
Registered
2020-06-03
Start date
2017-11-01
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

Knee osteoarthritis

Interventions

Pre-operative educational method, with pre-operative lectures about the pre, intra and post-operative of the total knee arthroplasty done by a nurse, a physical therapist and an orthopaedic surgeon (i
Behavioural

Sponsors

Marco Antonio Percope de Andrade
Lead Sponsor
Marco Antonio Percope de Andrade
Collaborator

Eligibility

Age
45 Years to 90 Years

Inclusion criteria

Inclusion criteria: Unilateral symptomatic primary or secondary OA of the knee; age of 45 years or older; indication of a primary total knee replacement; signed the informed consent form

Exclusion criteria

Exclusion criteria: Bilateral symptomatic osteoarthritis; not accept to participate in the study

Design outcomes

Primary

MeasureTime frame
To evaluate the range-of-motion of the knee measured by goniometric method. An increase of 20% is expected in the intervention group. ;It is expected an increase of 20% in the range of motion, in the group in which the intervention was done (differentiated orientation)

Secondary

MeasureTime frame
The purpose is to evaluate post-operative pain measured by visual analogic pain scale (VAPS). We estimate an 20% reduction of pain scale in the intervention group. ;SF36 and Womac functional scores will be evaluated in the pre and in the post-operative period. This outcome aim to analyze patient subjective satisfaction regarding surgical procedure. Intervention should increase more than 20% in the functional scores. ;Walk capacity will be evaluated measuring quantitatively the walk capability measured in block distance per day. A 30% increment in walk capability is expected in the intervention group.

Countries

Brazil

Contacts

Public ContactMarco Antonio;Marco Antonio Percope de Andrade;Percope de Andrade

Marco Antonio Percope de Andrade;Universidade Federal de Minas Gerais

mapa.bhz@terra.com.br;mapa.bhz@terra.com.br31992424449;=55-31-992424449

Outcome results

None listed

Source: REBEC (via WHO ICTRP)