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The Use of Laser in Runners with Achilles Tendonitis using Vascular Points Technique: A clinical, longitudinal, Interventional Study

Photobiomodulation in Runners with Achilles Tendinopathy using the Vascular Points Technique: Clinical, longitudinal, interventional study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-4pvhhg5
Enrollment
Unknown
Registered
2024-06-27
Start date
2024-07-01
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

Calcaneal tendon

Interventions

E02.594.540
E02.594
An interventional, longitudinal clinical study involving 91 male and female runners, with a regular exercise frequency of 2 times per week, diagnosed with calcaneal tendon tendinopathy, randomized int

Sponsors

Universidade São Francisco - USF
Lead Sponsor
Universidade Federal de São Paulo - Unifesp
Collaborator

Eligibility

Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Volunteers with insertional calcaneal tendon tendinopathy or in the tendon body, both genders, age between 18-55 years, runners (minimum 10-50 km per week) are in activity that present: symptoms and/or functional disability: VISA-A (4) during running activity; pain at tendon palpation; modified Blazin > 3; Evaluation of symptoms and functional capacity in Heel Rise and unipodal jump

Exclusion criteria

Exclusion criteria: Volunteer who has a history of previous lower limb surgery ; any physiotherapeutic treatment for calcaneal tendon tendinopathy in the last 6 months; individuals with a history of recent fracture and/or calcaneal tendon rupture; history of prolonged use of corticosteroids and/or anabolic steroids.

Design outcomes

Primary

MeasureTime frame
It is expected to find a reduction in pain within the vascular group, as assessed through the VISA-A questionnaire and the Numeric Pain Rating Scale (NPRS).;The expectation is to find an improvement in pain of more than 2 points on the END scale and in the VISA-A questionnaire, both pre and post intervention.

Secondary

MeasureTime frame
It is expected to find an increase in blood flow and oxygenation in the calcaneal tendon in the vascular group. verified by moorVMS-LDF-HP High Power Laser Doppler during the application of low intensity light therapy.;It is expected to observe an increase of at least 10% of the strength of the triceps sural muscle and lateral rotators of the hip, verified through the dynamometry evaluated in the pre and post intervention ;It is expected to observe a negative influence of psychological factors (self-efficacy and kinesiophobia) on pain and function, verified through the Scale of chronic pain and self-efficacy - PSEQ and Tampa scale in pre and post intervention

Countries

Brazil

Contacts

Public ContactUniversidade São Francisco - USF

Universidade São Francisco - USF

comiteetica@usf.edu.br55+(11)2454-8302

Outcome results

None listed

Source: REBEC (via WHO ICTRP)