Analyze the Relationship Between the Density of Fat Tissue and Cellulite With the Lumbar Lordosis Degree

March 6, 2018 updated by: Andreia Noites, Escola Superior de Tecnologia da Saúde do Porto

Analyze the Relationship Between the Density of Abdominal Visceral and Subcutaneous Fat and Cellulite With the Lumbar

The aim of this study is analyze the relationship between the density of visceral and subcutaneous fat and cellulite with the lumbar lordosis degree.

Study Overview

Status

Completed

Conditions

Detailed Description

There are two types of abdominal fat: subcutaneous adipose tissue which is more superficial, lying above the abdominal muscle wall and visceral adipose tissue, corresponding to the intra-abdominal fat witch is more harmful to health.

The accumulation of fat tissue differs between genders and age. Men have a huge propensity for developing central fat and women accumulate more subcutaneous fat tissue on the gluteal-femoral region. Some authors suggest that the accumulation of fat tissue increases with age.

Several studies have concluded that there is a relationship between the abdominal fat storage and the degree of lumbar curvature.

In addition, some authors also suggest that there is a relationship between the degree of lumbar lordosis and cellulite, which is related to circulatory changes.

However these relationships are not yet clarified in the literature.

Study Type

Observational

Enrollment (Actual)

20

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Porto
      • Vila Nova de Gaia, Porto, Portugal, 4400-303
        • Andreia Noites

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 60 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

All the comunity of the School of Allied Health Technologies

Description

Inclusion Criteria: All the community of the School of Allied Health Technologies; aged between 18-60

Exclusion Criteria: Pathologies (cardiovascular, metabolic, cancer, respiratory, muscular); pregnancy; abdominoplasty; collum and gluteal surgeries; deregulated menstrual cycle ; anatomical changes; anticelulitic treatments

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Case-Only
  • Time Perspectives: Retrospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Males
Evaluation of body mass index, determination of waist-to-hip ration and waist-to-height ration, using perimetry; evaluation of 7 skinfold according to the model 7-site-skinfold Equation, by Jackson and Pollock, and photogrammetry (to evaluate the lumbar lordosis degree) in males aged between 18 and 26.
Young Adults
Evaluation of abdominal thickness, percentage of abdominal fat and photogrammetry (to evaluate the lumbar lordosis degree) in young adults females aged between 18-26.
Adults
Evaluation of abdominal thickness, percentage of abdominal fat and photogrammetry (to evaluate the lumbar lordosis degree) in adult females aged between 40-60.
Females
Evaluation of body mass index, determination of waist-to-hip ration and waist-to-height ration using perimetry, evaluation of 7 skinfold according to the model 7-site-skinfold Equation, by Jackson and Pollock, and photogrammetry (to evaluate the lumbar lordosis degree) in females aged between 18 and 26.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evaluation of Lumbar Lordosis by analysing photos of the lateral right side of the participants
Time Frame: Day 1
We used photogrammetry for this evaluation. We marked the anatomical points (T11, L1, S2 and Antero-superior Iliac Spine) with isopod balls. We took a picture of the right lateral view of the participant. Finally we used the SAPo software to measure free angles to determinate lumbar lordosis degree.
Day 1

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Body Mass Index
Time Frame: Day 1
The height was measured by a tape-measure. We used the bioimpedance balance to determinate the body mass of the participants. BMI was calculated by using the body weight divided by height squared.
Day 1
Perimeters measurements using a tape-measure at waist level and at trochanters level at the end of expiration
Time Frame: Day 1
The perimeters measurements were done at the end of expiration, at waist level and at trochanters level. The waist-hip ratio was calculated by using the waist level perimeter divided by trochanters level perimeter and the waist-to-height ratio was calculated by using the waist level perimeter divided by height
Day 1
Skinfold measures
Time Frame: Day 1
Subscapular, tricipital, chest, axillar, suprailiac, abdominal, thick skinfolds were performed three times in right hemibody, by caliper according to the model 7-site-skinfold Equation, by Jackson and Pollock. Siri equation was used to determinate the percentage of total body fat.
Day 1
Bioimpedance Balance
Time Frame: Day 1
This instrument was used to determine the weight, the percentage of body and abdominal fat, the visceral index and the percentage of body and abdominal lean mass.
Day 1
Ecograph
Time Frame: Day 1
It was used for distinguishing of abdominal thickness fat (differentiate the fat in visceral and subcutaneous fat tissue) and in order to obtain the thickness of the subcutaneous adipose tissue at the points of maximum and minimum temperature on the gluteal region.
Day 1
Thermography
Time Frame: Day 1
Measurement of skin temperature in the gluteal region to obtain the average, the minimum and the maximum temperature on this area.
Day 1
Cellulite Grading Scale
Time Frame: Day 1
6 Photos were taken in the posterior and lateral (right and left) views, 3 in relaxation and 3 in gluteal isometric contraction.
Day 1

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
International Physical Activity Questionnaire
Time Frame: Day 1
International Physical Activity Questionnaire was used to monitor lifestyle
Day 1
Food Frequency Questionnaire
Time Frame: Day 1
Food Frequency Questionnaire was used to monitor lifestyle
Day 1

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Andreia Noites, PhD, Escola Superior de Tecnologia da Saúde do Porto

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

June 1, 2016

Primary Completion (Actual)

October 1, 2016

Study Completion (Actual)

July 1, 2017

Study Registration Dates

First Submitted

August 1, 2016

First Submitted That Met QC Criteria

September 12, 2016

First Posted (Estimate)

September 16, 2016

Study Record Updates

Last Update Posted (Actual)

March 7, 2018

Last Update Submitted That Met QC Criteria

March 6, 2018

Last Verified

March 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • AN-005
  • AR (Other Identifier: Escola Superior de Tecnologia da Saúde do Porto)
  • MS (Escola Superior de Tecnologia da Saúde do Porto)
  • MÇ (Escola Superior de Tecnologia da Saúde do Porto)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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