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Clinical Trials/NCT05966779
NCT05966779CompletedNot Applicable

Physical Therapy Intervention in the Immediate Postoperative Phase of Lipedema Surgery

University of Alcala1 site in 1 country293 target enrollmentStarted: July 1, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
293
Locations
1
Primary Endpoint
Pain Visual Analogue Scale

Study Overview

Brief Summary

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

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.

Study Design

Study Type
Observational
Observational Model
Ecologic Or Community
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

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

Arms & Interventions

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.

Intervention: modified CDT physical therapy protocol, based on Godoy's Method (Other)

Outcomes

Primary Outcomes

Pain Visual Analogue Scale

Time Frame: Baseline, short-term (post-treatment), and 90 days follow-up

Pain assessed using the Visual Analogue Scale (VAS). Scores range from 0 mm (no pain) to 100 mm (worst imaginable pain), where higher scores indicate worse pain.

Secondary Outcomes

  • mobility - scale(2018-2022)
  • edema resorption - volume(2018-2022)
  • patient satisfaction(2018-2022)
  • complications reported - binary outcome(2018-2022)

Investigators

Sponsor
University of Alcala
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ester Cerezo-Téllez

PhD., Professor

University of Alcala

Study Sites (1)

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