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Efffectiveness of a Roller Intervention in Anterior Knee Pain

Effectiveness of a Roller Intervention in Patients With Anterior Knee Pain: a Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03620799
Enrollment
15
Registered
2018-08-08
Start date
2018-08-15
Completion date
2018-09-30
Last updated
2018-08-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anterior Knee Pain Syndrome

Keywords

Roller intervention, Knee pain, Algometry

Brief summary

Anterior knee pain is one of the most frequent reasons for consultation within knee conditions in adolescents and young adults. However, despite the high prevalence of this disorder, its pathogenesis and therefore its treatment are not clearly understood. Foam rolling has become a common intervention to enhance joint mobility and muscle recovery after exercise. the aim of this study is analyze the effectiveness of a roller intervention in patients with anterior knee pain.

Detailed description

Randomized controlled trial. patients were divided into two groups, intervention and control.

Interventions

PROCEDUREManual therapy

A manual intervention technique is employed to the intervention group based on a roller treatment.

Sponsors

Universidad de Granada
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients between 18 and 65 years. * Knee anterior pain diagnosis

Exclusion criteria

* Concomitant somatic or psychiatric disorder * Previous knee surgery * Other lower limb traumatological pathologies

Design outcomes

Primary

MeasureTime frameDescription
Changes in mechanosensitivityChanges from baseline mechanosensitivity at 4 weeksMechanosensitivity is going to be assessed by a hand-held pressure algometer. The pressure will be applied perpendicular to the skin at a constant rate of 30 kPa/s until the patient felt the pressure change to pain and pressed a button defining the PPT.

Secondary

MeasureTime frameDescription
Vertical jump assessment with a matBaseline, 4 weeksThe subject started with the foot of the designated testing leg on the contact mat and their hands on their hips, they were then instructed to sink and hold a knee position (approximately 1208 knee angle), and the experimenter then counted out 4 s. On the count of four the subject was instructed to then jump as high as possible.
Isokinetic strengthBaseline, 4 weeksIsokinetic strength of the knee flexors and extensors of each leg will be measured using an isokinetic Biodex dynamometer (Biodex Corporation, Shirley, NY), which recorded instantaneous muscular torques.
Pain intensity assessed by the Brief Pain InventoryBaseline, 4 weeksPain will be assessed using the Brief Pain Inventory. The Brief Pain Inventory is a pain assessment tool used to measure pain intensity and pain interference. Patients rate the severity of their pain at its worst and least during the previous week, on average, and right now. Patients rate their level of pain interference in different contexts.
Functional knee limitation assessed by the Kujala Knee ScoreBaseline, 4 weeksThe Kujala Knee Score questionnaire will be selected for self-reported functional activity level of the patients. The composite score ranges from 0 to 100, with 100 indicating no functional limitation.

Contacts

Primary ContactMarie Carmen Valenza, PhD
cvalenza@ugr.es958242360

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026