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EFFECT OF CRYOTHERAPY ON KINEMATIC GAIT PARAMETERS IN PATIENTS WITH CHRONIC PATELLOFEMORAL PAIN SYNDROME

EFFECT OF CRYOTHERAPY ON KINEMATIC GAIT PARAMETERS IN PATIENTS WITH CHRONIC PATELLOFEMORAL PAIN SYNDROME

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06795269
Enrollment
60
Registered
2025-01-28
Start date
2023-10-08
Completion date
2024-12-20
Last updated
2025-01-28

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

Conditions

CHRONIC PATELLOFEMORAL PAIN SYNDROME

Keywords

Cryotherapy, compression cryotherapy, Biodex Gait Trainer

Brief summary

this study show the EFFECT OF CRYOTHERAPY ON KINEMATIC GAIT PARAMETERS IN PATIENTS WITH CHRONIC PATELLOFEMORAL PAIN SYNDROME and review its reliability. Participants were randomly allocated into two equal groups (A and B ) were done by a blinded independent researcher who opened enclosed envelopes containing computer generated randomization serially number index cards using statistical package for social science (SPSS),program (version 20 for windows ,spss, Chicago Illinois,USA) There were no dropouts among the participants throught the study after randomization.

Detailed description

Sixty patients from both genders were participated in this study. they were selected from the outpatient clinic of Faculty of Physical Therapy ,Cairo University with a PFPS. The Patients of both genders with their ages were ranging from 18 to 40 years old and their BMI was from 20 to 25 kg/m2. Thirty patients with PFPS, Their ages ranging from 18 to 40 years old ,Their BMI was from 20 to 25 kg/m2 received treatment in form of Traditional treatment (Strengthening exercise, Stretching, ultrasound and electrotherapy). The treatment performed three time a week for 4 weeks. Thirty patients with PFPS, Their ages ranging from 18 to 40 years old ,Their BMI was from 20 to 25 kg/m2 received treatment in form of Traditional treatment (Strengthening exercise, Stretching, ultrasound and electrotherapy) with cryotherapy, The treatment performed three time a week for 4 weeks.

Interventions

DEVICECryotherapy Compression Machine

The Cryo Pro is a simple to use cold compression therapy product that requires only ice, water and power. It's unique design is convenient to use, provides pain relief and reduces swelling and inflammation, making recovery faster.

OTHERConservative treatment

Strength and stretch exercises for hip and knee large groups of muscles.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* The patients were diagnosed as patellofemoral pain by an orthopedist. * The participants were eligible to be included if they had bilateral PFPS or unilateral PFPS. * Duration of knee pain is 4-5 weeks during 6 months prior to study. (Collins et al., 2010). * Their ages were ranging from 18 to 40 years (Clin Rheumatol et al., 2012). * Their BMI was ranging from(20 to 25 kg/m2) (Fischer et al., 2009)

Exclusion criteria

* • Rheumatoid Arthritis or other systemic rheumatic diseases. * Dementia, psychosis. * Active substance abuse disorder; acute or chronic disease, injury, deformity. * Operation of the lower limb and knee. * Severe hearing or visual impairment. * Hospitalization for a cardiovascular condition, cerebral infarction or arrhythmia in the previous 3 months. * Recent history of 3 or more falls. * Current participation in another OA intervention study. * Uncontrolled diabetes mellitus. * Intra-articular knee injections in the previous 6 months. * Contraindications to cryotherapy application those that feel a high level of discomfort or pain during the application.

Design outcomes

Primary

MeasureTime frameDescription
Biodex Gait Trainer4 weekstreadmill with real-time step length visualization (where the foot was placed) was used to assess the selected spatiotemporal gait parameters. During the test, the patient was visually informed about the suggested foot placement/planned length of the step. This three-minute extended test was conducted before and after the rehabilitation program.

Countries

Egypt

Outcome results

None listed

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