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Effects of taping in pain and function of patients with knee arthrosis: a blind randomised clinical trial

Effectiveness of taping in pain and functional capacity of patients with knee osteoarthritis: a blind randomised clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-54pbt6
Enrollment
Unknown
Registered
2015-10-22
Start date
2015-05-13
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

control group: 40 patients will undergo stretching exercises, strengthening and balance training lasting 60 minutes each therapy, 2 times per week over 8 weeks. Intervention group: 34 patients will un
Other
E02.779.483.750
E01.370.600.425

Sponsors

Universidade Federal de São Paulo
Lead Sponsor
AACD - Associação de Assistência à Criança Deficiente
Collaborator

Eligibility

Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 74 Adult patients (18 from 80 years) referred AACD - Lar Escola São Francisco diagnosed with moderate knee osteoarthritis and agree to participate in the study according to the term informed consent

Exclusion criteria

Exclusion criteria: Patients with rheumatic diseases associated; orthopedic surgery of the lower limbs; prior injections of steroids in the past six months; obesity (BMI> 35);allergy to components of physiotherapy; those who underwent physiotherapy in the last six months.

Design outcomes

Primary

MeasureTime frame
Primary outcome : pain The level of pain pain is measured by Visual Analogue Scale that it is a graduated scale ranging from 0 to 10 , where the higher the number , the higher is the level of pain . This scale will be applied by by an independent observer blind , at baseline ( pre-intervention ) after four and eight weeks of treatment. It is expected that the application of banding associated with the exercise program ( intervention group ) provides pain relief of at least 5 % compared with the control group, which only perform the therapy based exercise program.

Secondary

MeasureTime frame
Secondary outcome : function Functional capacity will be assessed by WOMAC questionnaire containing 17 questions about the degree of difficulty in performing activities of daily living . The questionnaire will be applied by an independent observer blind , at baseline ( pre-intervention ) and after eight weeks of treatment. It is expected that the use of banding associated with the exercise program ( intervention group ) provide patients better functional outcomes ( at least 5% ) compared with control patients , which performs the same therapy exercises, but without the additional use of bandage.

Countries

Brazil

Contacts

Public ContactJosé ;José Baldocchi Pontin;Jardim

AACD - Associação de Assistência à Criança Deficiente;Universidade Federal de São Paulo

zeca.fisio13@hotmail.com;jardimpneumo@gmail.com+ 55 (11) 5904-8000;+55 (11) 983662625

Outcome results

None listed

Source: REBEC (via WHO ICTRP)