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Physiotherapy resources in the treatment of localized fat

Electrothermalphototherapy agents in the treatment of the Body Disharmony Syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-96sw76
Enrollment
Unknown
Registered
2016-11-16
Start date
2016-09-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Localized abdominal adiposity or subcutaneous fat

Interventions

This is a prospective randomized clinical study, exploratory, quantitative approach, performed in accordance with Consolidated Standards of Reporting Trials (CONSORT) guidelines (SCHULZ, ALTMAN and HO
aged 18 to 40
sedentary
with the presence of fat located in the abdominal area. Women eligible for the study will be invited to participate through verbal invitation, publicity posters and dissemination electronically. Those
nutritional status (Food Frequency Questionnaire)
level of physical activity (International Physical Activity Questionnaire / IPAQ)
body mass index
waist-hip ratio
abdominal circumference
adipometria and fat percentage
abominal ultrasound
resistance of the flexor muscles of the trunk
photographic record of abodminal region
range of personal satisfaction. Then the application of assessment tools, the participants (n=180) will be randomized into 6 grou
Other
E02.565.280.945
E02.331

Sponsors

Universidade Federal do Paraná
Lead Sponsor
Universidade Federal do Paraná
Collaborator

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Healthy volunteers; women; aged 18 to 40; sedentary; with the presence of fat located in the abdominal area.

Exclusion criteria

Exclusion criteria: Women in diet; with smoking and drinking habits; women using drugs for weight loss, steroids, progesterone and diuretics; pregnant women; mothers less than one year, women who have electronic monitoring; women with metal implants in the pelvic area; women who are in dermatofuncional treatment on site; surgery and / or radiation therapy for less than 6 months of the abdominal / pelvic area; women suffering from lymphatic system disorders, thrombophlebitis, acute infection, central nervous system diseases, tumors and diabetes, abnormal sensitivity.

Design outcomes

Primary

MeasureTime frame
Reduction of abdominal subcutaneous fat verified by ultrasound from the realization of a range of at least 5% in the pre and post intervention.

Secondary

MeasureTime frame
Reduction of subcutaneous fat through the finding adipometria from a variation of at least 5% in pre and post intervention.

Countries

Brazil

Contacts

Public ContactRaciele Korelo

Universidade Federal do Paraná

raciele_guarda@yahoo.com.br+55 (41) 9177 6161

Outcome results

None listed

Source: REBEC (via WHO ICTRP)