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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04481022
Other study ID # PFPS clinical prediction rule
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 3, 2020
Est. completion date August 30, 2021

Study information

Verified date September 2020
Source Cairo University
Contact khaled AlaaEldin Fetouh, Master
Phone 01090737464
Email drkhaled929292@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

the aim of study is to investigate the effect of body mass index (BMI), age, duration of symptoms, pain severity and knee angle valgus on patient̀•̀•s response to proximal control exercises.


Description:

Patellofemoral pain syndrome (PFPS) is recognized as one of the most common lower-extremity disorders encountered by orthopaedic physical therapists. Females were 2.23 times more likely to develop PFPS than males. Various authors have suggested that hip weakness may be an impairment associated with PFPS, because poor hip control may lead to abnormal lower extremity or patellofemoral motions. Clinical prediction rules (CPRs) are tools designed to improve decision making in clinical practice by assisting practitioners in making a particular diagnosis, establishing a prognosis, or matching patients to optimal interventions.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date August 30, 2021
Est. primary completion date April 30, 2021
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria:

- Age 18 to 35 years.

- Anterior or retropatellar knee pain of non-traumatic origin that was greater than six weeks duration and provoked by at least two predefined activities (prolonged sitting or kneeling, squatting, jogging or running, hopping, jumping, or stair walking).

- Pain on palpation of the patellar facets, or with step down from a 15 cm step, or double leg squat.

Exclusion Criteria:

1. Concomitant injury or pathology of other knee structures.

2. Previous knee surgery.

3. patellofemoral instability (history of sublaxation or dislocation; positive apprehension test).

4. knee joint effusion.

5. Osgood-Schlatter's.

6. hip or lumbar spine pain (local or referred).

7. physiotherapy within previous year; prior foot orthoses treatment or use of anti inflammatories or corticosteroids.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
proximal control exercises
study investigates the effectiveness of proximal control exercises for patients with PFPS in improving pain and function. The findings of this systematic review are consistent with previous evidence reporting effectiveness of exercise for PFPS. In particular, there is consistent moderate to high quality evidence (three RCT, one CCT, three cohort studies, and one case series) that proximal interventions provide relief of pain and improved function in the short term, whereas the knee programs have variable effectiveness. Physical therapists should consider using proximal interventions for early stage treatment for PFPS (Peters et al., 2013). After 4 weeks of a combined knee and hip strengthening exercise program, sedentary females with PFPS had a greater reduction in pain during stair descent compared to the group who performed knee strengthening exercises only. Both groups also showed significant improvement in function and pain during stair ascent (Fakuda et al., 2010).

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

References & Publications (3)

Earl JE, Hoch AZ. A proximal strengthening program improves pain, function, and biomechanics in women with patellofemoral pain syndrome. Am J Sports Med. 2011 Jan;39(1):154-63. doi: 10.1177/0363546510379967. Epub 2010 Oct 7. — View Citation

Lesher JD, Sutlive TG, Miller GA, Chine NJ, Garber MB, Wainner RS. Development of a clinical prediction rule for classifying patients with patellofemoral pain syndrome who respond to patellar taping. J Orthop Sports Phys Ther. 2006 Nov;36(11):854-66. — View Citation

Robinson RL, Nee RJ. Analysis of hip strength in females seeking physical therapy treatment for unilateral patellofemoral pain syndrome. J Orthop Sports Phys Ther. 2007 May;37(5):232-8. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary level of pain visual analogue scale 100-mm horizontal line anchored by word descriptors at each end by no the left and worst imaginable pain on the right baseline
Primary functional status Kujala questionnaire is a 13-items knee specific self-report questionnaire. It documents response to six activities thought to be associated specifically with anterior knee pain syndrome (walking, running, jumping, climbing stairs, squatting, and sitting for prolonged periods with knees bent), as well as symptoms such as limp, inability to bear weight through the affected limb, swelling, abnormal patellar movement, muscle atrophy and limitation of knee flexion. This questionnaire was used to ssess the individual's functional status and PFPS experienced during specific functional tasks. baseline
Primary Dynamic knee valgus 2d frontal plane projection angle 2D frontal plane projection angle (FPPA) analysis to measure dynamic knee valgus. for 2D FPPA analysis, the centers of each of hip, knee and ankle joints will be determined using a standard tape measure, markers will be placed at the midpoint of the ankle malleoli for the center of the ankle joint, midpoint of the femoral condyles to approximate the center of the knee joint, and on the proximal thigh at the midpoint of the line from the anterior superior iliac spine to the knee joint center. baseline
Secondary isometric muscle power of hip abductor and external rotation Hand held dynamometer will be used to asses isomteric hip abductor and isometric hip external rotator power baseline