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Photobiomodulation associated with short-term Eccentric Exercise Protocol on pain intensity and function in patients with Lower Limb Tendinopathy

Single or Cluster Photobiomodulation, associated with the Eccentric Exercise Protocol in patients with patellar and Achilles tendinopathy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-9vjfmz
Enrollment
Unknown
Registered
2018-09-24
Start date
2018-04-30
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

tendinopathy

Interventions

There are 2 groups and each one will consist of 21 participants who will perform the protocol of eccentric exercises followed by stretching and after that will perform the photobiomodulation (PBM) in
Device
E02.774
E02.760.169.063.500.387.875

Sponsors

Departamento de Ciências do Movimento Humano da universidade federal de São Paulo
Lead Sponsor
Departamento de Ciências do Movimento Humano da universidade federal de São Paulo
Collaborator

Eligibility

Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Participants aged between eighteen and fifty years with medical diagnosis of patellar tendon or tendon tendon disease for at least 3 months and have a VISA score (P and A) of less than 80 points without treatment for at least 3 months and signed the term of free and informed consent.

Exclusion criteria

Exclusion criteria: Individuals with neurological disorders that affect cognitive behavior and pain perception; conditions in the knee or ankle region (such as rheumatoid arthritis; osteoarthritis or fractures) that make it impossible to perform the assessments or protocol proposed; pregnancy; previous surgical procedure in the tendon; use of non-steroidal anti-inflammatory drugs (NSAIDs) during the last 2 weeks; injection of corticosteroids; diabetes mellitus and uncontrolled hypertension.

Design outcomes

Primary

MeasureTime frame
Improve pain and function analyzed by VISA-P Questionnaire with an increase of 13 point at least at the end of the study.

Secondary

MeasureTime frame
Pain improvement measured through NRS-11 with a 2-point decrease in pain intensity in the activity that causes the most pain at the end of the study

Countries

Brazil

Contacts

Public ContactMariana Ventura

Universidade Federal de São Paulo

mariana_ventura271@hotmail.com+55-13-991206636

Outcome results

None listed

Source: REBEC (via WHO ICTRP)