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Completed

NCT Number: NCT06795269

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

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.

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Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Physical Therapy College of Cairo University

Giza, Giza Governorate, 12613, Egypt

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Cryotherapy Compression Machine

Device

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.

Conservative treatment

Other

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

Primary outcomes

  1. Biodex Gait Trainer

    Time frame: 4 weeks

    treadmill 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.

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Jan 28, 2025
Registry last updated
Jan 28, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.