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Evaluation of a Polymeric Plate Derived From Castor Oil to Thermotherapy

Evaluation of a Polymeric Plate Derived From Castor Oil to Thermotherapy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01100541
Enrollment
30
Registered
2010-04-09
Start date
2010-02-28
Completion date
2010-02-28
Last updated
2010-04-09

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

Conditions

Polymers, Therapeutic Hyperthermia, Thermotherapy

Keywords

Therapeutic Hyperthermia, Thermotherapy, Polymers, Castor Oil

Brief summary

The objective of this work is to evaluate, from volunteers viewpoint, the usability, comfort, appearance, weight, superficial temperature, and other characteristics of a polymeric plate derived from castor oil developed to thermotherapy. The volunteers will use polymeric plate as a therapeutic resource in the shoulder area and then fill in, without interference of the researcher, some questions about the characteristics of interest.

Detailed description

In this study, the polymeric plate is prepared using the following procedure: 1. \- the water is heated to the boiling temperature 2. \- the heater is shut down 3. \- the polymeric plate is immersed in water 4. \- it rests in the water for 15 minutes 5. \- it is inserted in a wrap In this condition, the polymeric plate is placed on the shoulder of the volunteer and remains there for 20 minutes. After application, the volunteer answers the questionnaire containing eight questions on a Likert scale (0 to 10) and an area of observations. Previous laboratory tests were performed to ensure that the temperature of the polymeric plate will not cause skin burn in this application condition.

Interventions

DEVICEPolymeric plate

Application of the polymeric plate in the shoulder for 20 minutes after warming it for 15 minutes in hot water, initially at boiling temperature.

Sponsors

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.
CollaboratorOTHER_GOV
University of Sao Paulo
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Good communication and comprehension * Skin integrity

Exclusion criteria

* Reduced skin sensitivity * Disturbance in the central nervous system

Design outcomes

Primary

MeasureTime frameDescription
Acceptance of the polymeric plate2 weeksAcceptance of the polymeric plate by the volunteers.

Secondary

MeasureTime frameDescription
Polymeric plate temperature2 weeksPerception of the volunteers about the polymeric plate temperature.
Polymeric plate time of heat retention2 weeksPerception of the volunteers about the polymeric plate time of heat retention.
Sensation on the superficial touch of the polymeric plate2 weeksPerception of the volunteers about the sensation on the superficial touch of the polymeric plate.
Polymeric plate comfort2 weeksPerception of the volunteers about the comfort of the polimeric plate.
Polymeric plate weight2 weeksPerception of the volunteers about the polymeric plate weight.
Polymeric plate practicality2 weeksPerception of the volunteers about the polymeric plate practicality.
General observations about the polymeric plate2 weeksGeneral comments, suggestions and complaints of the volunteers about the polymeric plate.
Appearance of the polymeric plate2 weeksPerception of the volunteers about the appearence of the polymeric plate.

Countries

Brazil

Outcome results

None listed

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