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Diacutaneous Fibrolysis and Patellofemoral Pain Syndrome

Effectiveness of Diacutaneous Fibrolysis Technique on Pain, Range of Motion, Strength and Function in Patients With Patellofemoral Pain Syndrome

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02379364
Enrollment
60
Registered
2015-03-04
Start date
2015-05-31
Completion date
2016-05-31
Last updated
2017-05-11

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

Conditions

Patellofemoral Pain Syndrome

Keywords

Physiotherapy, Patellofemoral Pain Syndrome, Manual therapy

Brief summary

The aim of the study will be to assess the effectiveness of Diacutaneous Fibrolysis technique on pain, range of motion (Patellofemoral joint mobility test and muscle length test), strength and function in patients with Patellofemoral Pain Syndrome and muscle shortening. Muscle imbalance is one of most important factor associated with Patellofemoral Pain Syndrome. Shortening of lateral muscles of the thigh have a close relationship with patella position and tracking and patellofemoral pain. The scientific evidence for effectiveness of any soft tissue mobilization technique in patellofemoral pain syndrome patients is poor. Diacutaneous Fibrolysis is a non-invasive physiotherapeutic technique to release adherences and fibrosis between the different musculoskeletal structures. Diacutaneous Fibrolysis is applied by a set of metallic hooks having the advantage of allowing a deeper and more precise application, which could not be achieved manually. The present study evaluates the effectiveness of Diacutaneous Fibrolysis technique applied in the soft tissues more related with patellofemoral pain.

Interventions

Diacutaneous Fibrolysis is a non invasive physiotherapeutic technique applied by means a set of metallic hooks having the advantage of allowing a deeper and more precise application, which could not be achieved manually

Sponsors

Universidad de Zaragoza
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
16 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Unilateral or bilateral patellofemoral pain longer than three months * Anterior or retropatellar pain of non-traumatic origin that is provoked by at least two of the following activities: prolonged sitting or kneeling, squatting, running, hopping, jumping, or stair ascending/descending. * The presence of pain on palpation of the patellar facets, on step down from 25 cm step, or during a double leg squat. * Pain over the previous week equal to or greater than 3 on a 10-cm visual analogue scale. * The presence of muscle shortening in rectus femoris or tensor fascia lata muscle length test and/or hypo-mobility or stiffness in the compartmental muscle play.

Exclusion criteria

* Previous knee surgery or traumatic lesions * Concomitant injury or pathology of other knee structures * History of patella subluxation or dislocation * Evidence of knee joint effusion * Pain in and/or referred from the hip or lumbar spine * Currently undergoing physiotherapy treatment for Patellofemoral pain syndrome or use anti-inflammatories or corticosteroid medication at the same time of the study. * Subjects unable or unwilling to give informed to written consent or fulfil questionnaires.

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in pain intensity2 weeksVisual analogue scale (VAS)

Secondary

MeasureTime frameDescription
Muscle Length Test2 weeksRange of motion measured by digital inclinometer in hip adduction for iliotibial band, knee flexion for rectus femoris muscle and knee extension for hamstrings muscles
Isometric Strength of Quadriceps Muscle2 weeksdigital dynamometer
Pressure Pain Threshold2 weeksPressure algometry
Functional Status and disability2 weeksAnterior Knee Pain Scale
Global Rating of Change Scale2 weeksglobal improvement on a five point Likert scale and visual analogue scale
Functional Capacity2 weeksUnilateral squat test and step test for assessing functional capacity

Countries

Spain

Outcome results

None listed

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