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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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REBEC |
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Last refreshed on:
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29 May 2023 |
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Main ID: |
RBR-7w4cp9 |
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Date of registration:
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17/09/2018 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Effectiveness of Osteopathy in Patients with Knee Pain
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Scientific title:
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Effects of Osteopathic Manipulative Treatment on Patellofemoral Pain Syndrome of Runners Athletes: A Randomized Clinical Trial |
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Date of first enrolment:
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01/09/2018 |
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Target sample size:
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Recruitment status: |
Data analysis completed |
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URL:
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http://ensaiosclinicos.gov.br/rg/RBR-7w4cp9 |
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Study type:
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Intervention |
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Study design:
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Clinical trial of treatment, parallel, oneblind, randomized-controlled with 3 arms
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Phase:
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N/A
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Countries of recruitment
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Brazil
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Contacts
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Name:
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julio zago
guglielmin |
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Address:
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rua 24 sul lote 25
71927-000
brasília
Brazil |
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Telephone:
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+55-61-996566627. |
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Email:
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juliozagofisio@hotmail.com |
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Affiliation:
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Faculdade de Ceilândia |
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Name:
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julio zago
guglielmin |
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Address:
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rua 24 sul lote 25
71927-000
brasília
Brazil |
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Telephone:
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+55-61-996566627. |
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Email:
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juliozagofisio@hotmail.com |
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Affiliation:
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Faculdade de Ceilândia |
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Key inclusion & exclusion criteria
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Inclusion criteria: Athlete practicing running; between 18 and 35 years.
Exclusion criteria: Cognitive, musculoskeletal or psychiatric disorders; uncontrolled diabetes mellitus; history of recent infection (last 03 months); use of corticosteroids.
Age minimum:
18Y
Age maximum:
35Y
Gender:
-
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Health Condition(s) or Problem(s) studied
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Musculoskeletal Diseases; Patellofemoral pain syndrome.
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C05.550.700
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Intervention(s)
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E02.760.169.063.500.387
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Other
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Experimental group Osteopathic Treatment: Athletes will receive six sessions of osteopathy for three weeks. Experimental group Exercise Protocol: Athletes will receive six exercise sessions over three weeks.
Control group: athletes will not receive active treatment, they will only be evaluated during six sessions, for three weeks.
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E02.190.599
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Primary Outcome(s)
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To evaluate the patellofemoral pain in runners, verified through the visual analogue scale, based on the observation of a variation of at least 5% in pre and post-intervention measurements.
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Secondary Outcome(s)
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To evaluate the plantar pressures of runner athletes, verified by static baropodometry from the finding of a variation of at least 5% in the pre and post-intervention measurements.
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To evaluate the functionality of runner athletes, verified through the Lysorn Knee Scoring questionnaire and the dynamic valgus thesis, by observing a variation of at least 5% in the pre and post-intervention measurements.
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Source(s) of Monetary Support
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Faculdade de Ceilândia
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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