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Effect of Two Methods for the Application of Cryotherapy

Effect of Two Methods for the Application of Cryotherapy in Pain and Surface Temperature of the Skin in Women With Previous Pain in the Knee

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03707327
Enrollment
12
Registered
2018-10-16
Start date
2018-10-20
Completion date
2019-09-20
Last updated
2018-10-16

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

Conditions

Pain

Keywords

pain, knee, cryotherapy

Brief summary

Introduction: Little is known about the effects of different cryotherapy techniques for pain and skin surface temperature in patients with anterior knee pain. Objective: To analyze the best technique of cryotherapy intervention to reduce the superficial temperature of the skin and pain of women with anterior pain in the knee. Methodology: The sample will be composed of 12 participants, of the female gender, aged between 18 and 25 years old and complaint of anterior pain in the knee, distributed in cryotherapy groups by ice pack (CPG) (n = 6) and cryotherapy + compression group byGame Ready (CCGR) (n = 6). All will complete the consent form, the sample characterization form, the Visual Analog Pain Scale (EVA) and the Patellofemoral Disorders Scale (AKPS). They will then have the basal temperature of the anterior knee region recorded by thermographic camera and perform five repetitions of the sit and stand test in 30 seconds. The EVA will again respond and the temperature of the anterior knee region will be collected after the test. Subsequently, CPG or CCGR (randomly) will be applied to the anterior region of the knee for 20 minutes. Immediately after the application of cryotherapy, EVA will be applied and will have the skin surface temperature recorded immediately after, and at 10, 20, 30 and 60 minutes. Expected results: It is expected to establish if there is difference in pain, surface temperature and skin reheating of women submitted to cryotherapy by ice pack and Game Ready.

Detailed description

After the contact, explanation of the study procedures and acceptance of the participants, the data collection will be started and performed in the teaching laboratory of the Physiotherapy course of the State University of Londrina. Initially, the demographic data of the sample (age, height, weight, limb and time of pain) and signature of the consent term will be collected. After this step, the participants should point to the Visual Analogue Scale (EVA) and the Patellofemoral Disorders Scale (AKPS). Before performing the cryotherapy technique, the basal skin temperature in the anterior region of the knee will be recorded by means of a thermographic camera, and the participants will be submitted to five sets of the sit and stand test in 30 ', with rest of one minute between them. They will then re-signal the EVA and the skin temperature will be retained by the camera. Finally, they will undergo the application of cryotherapy according to the category which has been randomized. The two different intervention techniques will be: * Ice pack group (CPG): where the participant will have a plastic bag containing 500 grams of crushed ice over the anterior region of the knee, and lie flat with the lower limb extended and supported on the ground for 20 minutes; * Group Cryotherapy + Compression by Game Ready® (CCGR): where the participant will have the knee joint wrapped and compressed by the equipment where temperature, compression and time will be controlled, maximum compression, for 20 minutes by the equipment itself; lie in the same manner as for the other intervention. Immediately thereafter, the EVA will be applied and the skin surface temperature recorded in the knee region, as well as 10, 20, 30 and 60 minutes thereafter.

Interventions

the participants remained for 20 minutes with intermittent compression therapy + cryotherapy

the participants remained for 20 minutes with cryotherapy with ice pack

Sponsors

Universidade Estadual de Londrina
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 25 Years
Healthy volunteers
Yes

Inclusion criteria

* women * anterior knee pain

Exclusion criteria

* muscle or joint injuries in the last month * vascular problems * allergy to cold * lower limb surgery in the last 6 months * viral conditions (such as colds or flu)

Design outcomes

Primary

MeasureTime frameDescription
Painpreheatingmeasurement pain by analogue visual scale (Score zero to ten, when zero is painless and 10 is maximum pain)

Secondary

MeasureTime frameDescription
Temperturepreheatingthrough thermographic camera
Temperatureafter 60 minutesthrough thermographic camera

Contacts

Primary ContactFernanda B Pesenti, Ma
fernanda_pesenti@hotmail.com+55 43 3371 2490
Backup ContactChristiane G Macedo, PhD
chmacedouel@yahoo.com.br+55 43 3371 2490

Outcome results

None listed

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