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Influence of core muscles in women with patellofemoral pain syndrome

Influence of core muscles in women with patellofemoral pain syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-7fk9ww
Enrollment
Unknown
Registered
2018-10-01
Start date
2018-06-06
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

Patellofemoral Pain Syndrome

Interventions

The study has only one intervention group with 20 subjects, which is based on a program of therapeutic exercises to strengthen the core muscles with a duration of 12 weeks performed 3 times a week, wi
Other
E02.760.169.063.500.387

Sponsors

Universidade Federal de Santa Catarina
Lead Sponsor
Universidade Federal de Santa Catarina
Collaborator

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: retropatellar or anterior knee pain during at least two of the following activities: sitting for an extended time, climbing stairs, crouching, running, kneeling, and jumping; pain during patellar palpation; symptoms for at least 1 month, insidious onset and unrelated to the traumatic accident; pain level at least 3 on a visual analogue scale of 10cm, in the last week; More than 3 positive of the following clinical signs: Clarke test, McConnell test, Waldron test, Zohler test, upper Q test greater than 18 degrees, Noble compression test, lateral or medial patella positioning; women aged between 18 and 35 years; Ability to perform normally as activities of daily living.

Exclusion criteria

Exclusion criteria: Other specific knee conditions such as gonarthrosis, ligament injury, meniscus injury, patellar tendon injury, joint degeneration, osteoarthritis or referred pain from the spine; knee surgery; history of patellar displacement or subluxation; knee treatments such as arthroscopy, use of anti-inflammatories, analgesics, anesthetics, acupuncture or physiotherapy during the last 6 months; presence of neurological diseases and inflammatory processes.

Design outcomes

Primary

MeasureTime frame
After a 12-week intervention program the pain level will be evaluated by the Visual Analog Scale and muscular activation level (mV) through surface electromyography.

Secondary

MeasureTime frame
After a 12-week intervention program the index of functionality will be evaluated by the Function Index Questionnaire (FIQ) and core muscle strength through the "board" resistance test.

Countries

Brazil

Contacts

Public ContactHeloyse Kuriki

Universidade Federal de Santa Catarina

heloyse.kuriki@ufsc.br+55(048)37216952

Outcome results

None listed

Source: REBEC (via WHO ICTRP)