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Clinical efficacy of a distance exercise protocol associated with telephone professional follow-up for patients with chronic knee pain

Clinical efficacy of a distance exercise protocol associated with telerehabilitation for patients with chronic knee pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-7t5bhh
Enrollment
Unknown
Registered
2019-04-03
Start date
2018-11-09
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

Telerehabilitation group: 20 participants of both sexes aged 45 years or more, will be submitted to the telereabilitation protocol. These individuals should perform a series of physical exercises cont
Other

Sponsors

Universidade Federal de São Carlos
Lead Sponsor
Universidade Federal de São Carlos
Collaborator

Eligibility

Age
45 Years to No maximum

Inclusion criteria

Inclusion criteria: It will be included participants aged greater than or equal to 45 years, with chronic knee pain, defined by the International Association for the Study of Pain (IASP) as recurrent pain for at least 3 months, (score 4 on the Visual Analogue Pain Scale [EVA]) and medium to moderate physical dysfunction (score> 20 of 68 on the Western Ontario and McMaster Universities Osteoarthritis Index [WOMAC]).

Exclusion criteria

Exclusion criteria: Subjects who have undergone knee arthroplasty or other lower limb surgery will be excluded from the study, are already undergoing any treatment or exercise program, have any neurological or cardiovascular conditions that limit exercise and do not have access to a telephone.

Design outcomes

Primary

MeasureTime frame
It is hoped that the volunteers who make a protocol of exercises at a distance together with telerehabilitation will have a clinical improvement, characterized by an improvement in functional activities (verified by the functional tests and WOMAC questionnaire) and decrease in pain intensity (verified by Analog Visual Scale - EVA), higher than those who only make the protocol.

Secondary

MeasureTime frame
Secondary outcomes are not expected

Countries

Brazil

Contacts

Public ContactJéssica Bianca;Jéssica Bianca Aily;Aily

Universidade Federal de São Carlos;Universidade Federal de São Carlos

je.aily@hotmail.com;je.aily@hotmail.com+55(16)33519579;(16) 3351-9579

Outcome results

None listed

Source: REBEC (via WHO ICTRP)