Cellulite
Conditions
Interventions
This is a randomized, two-arm, double-blind, quantitative clinical study involving 200 women aged 18 to 45, randomly divided into two groups of 100 participants each. Intervention group: 100 women wil
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Sponsors
Universidade Federal de Alfenas - UNIFAL-MG
Universidade Federal de Alfenas - UNIFAL-MG
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: Participants must be female; aged between 18 and 45 years at the date of assessment; have signed the informed consent form; report fibroedemageloid, confirmed using a validated scale; women who are menstruating on the day of assessment will not be included and will be rescheduled for a new date
Exclusion criteria
Exclusion criteria: Pregnant women; women in menopause; with history of orthopedic injury and/or surgery in the lower limbs within the last six months; dermatological lesions such as ulcers or surgical scars; undergoing aesthetic treatment in the evaluated region; history of neurological, rheumatological, or endocrine diseases diagnosed within the last year; volunteers who have not signed the informed consent form
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in perception of geloid fibroedema and muscle strength in healthy women, measured by subjective perception scale, ultrasound and thermometry, comparing baseline values ??(day before the start of the intervention) with values ??after 8 weeks of continuous use of the insoles | — |
Secondary
| Measure | Time frame |
|---|---|
| Change in the classification of geloid fibroedema in healthy women, comparing the stage before the start of the intervention with those observed after 8 weeks of using the insoles | — |
Countries
Brazil
Contacts
Public ContactLeonardo Carvalho
Universidade Federal de Alfenas
Outcome results
None listed