Physical Therapy in Lipedema Surgery

NCT ID: NCT05966779

Last Updated: 2023-08-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

293 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-07-01

Study Completion Date

2023-07-12

Brief Summary

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The goal of this observational study or clinical trial is to know evaluate the effects of a modified Complete Decongestive Therapy protocol using the Godoy Method in the postoperative period following lipedema surgery.

The main question it aims to answer are:

* if the treatment is effective on pain reduction, edema resorption, mobility improvement in short term and follow-up at 90 days
* if the treatment is effective on preventing complications of these participants after surgery

Participants have been treated in the lasts years and authors recover information of the effects of the treatment.

Researchers will compare sub-groups of participants depending on the number of physical therapy sessions received

Detailed Description

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Background: Lipedema is an adipose tissue disorder in women, with an abnormal fat deposition in lower limbs and occasionally upper limbs. The patients present pain, bruising, heaviness, and mobility impairment. It affects them physically and psychologically. Purpose: This study aims to evaluate the effects of a modified CDT protocol using the Godoy Method in the postoperative period following lipedema surgery.

Outcomes: pain (VAS), edema resorption, complications, mobility and patient satisfaction.

A descriptive statistical analysis will be performed using means and standard deviation (quantitative outcomes) and percentages (dichotomous and categorical outcomes). An inferential analysis will be carried out using paired and unpaired T-tests as One-way and repeated measures ANOVA to search for differences between quantitative outcomes. Pearson chi-square will also be used to relate dichotomous and categorical variables in a transversal analysis. All missing values will be excluded from the analysis. In all cases, a P\<0.05 value and a 95% confidence interval will be determined forstatistical significance. All statistical analysis will be performed using the Stata® version 14.2 package for MS Windows® version 10.

Conditions

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Assessment Lipedema Vascular Diseases Dermatologic Complication

Study Design

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Observational Model Type

ECOLOGIC_OR_COMMUNITY

Study Time Perspective

RETROSPECTIVE

Study Groups

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modified CDT physical therapy protocol, based on Godoy's Method

A complete physical therapy assessment was done. All sociodemographic data were recruited as well as body mass index (BMI), the month of intervention, kind of surgery, extracted liters, psychological treatment, physical therapy sessions, pain, mobility, complications (seroma, wound infection, chafing or risk of ulcer, pain, fibrosis, genital edema), compression, smoking, satisfaction with the treatment received.

A modified CDT physical therapy protocol, based on Godoy's Method, was applied to all study participants. This protocol comprised of

1. Cervical Stimuli 15min
2. MLD based on Godoy
3. Mechanical lymphatic drainage with RA Godoy® device
4. Compression therapy with multilayer and multicomponent bandages during the mechanical lymphatic drainage.
5. Skin care - before and after the bandages- and therapeutic education.
6. Put on compression garments
7. Active movement if possible.

modified CDT physical therapy protocol, based on Godoy's Method

Intervention Type OTHER

modified CDT physical therapy protocol

Interventions

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modified CDT physical therapy protocol, based on Godoy's Method

modified CDT physical therapy protocol

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* female subject who underwent a lipedema surgery
* recommendation of the surgeon to receive physical therapy

Exclusion Criteria

* unilateral surgery
* lack of data in the clinical history
* only 1-2 physical therapy sessions
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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University of Alcala

OTHER

Sponsor Role lead

Responsible Party

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Ester Cerezo-Téllez

PhD., Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Ester Cerezo Tellez

Alcalá de Henares, Madrid, Spain

Site Status

Countries

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Spain

Other Identifiers

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OE36/2023

Identifier Type: -

Identifier Source: org_study_id

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