High-heeled Shoes in a Sample of Young Women

February 22, 2024 updated by: Manusapiens

Repercussions on Spinal Posture Before and After Wearing High-heeled Shoes in a Sample of Young Women: Cross-sectional Pilot Study

At a postural level, many doctors, physiotherapists and chiropractors are convinced that lower back pain induced by heels is due to an increase in lumbar lordosis associated with an anterior pelvic tilt; this thought is even shared by the American Chiropractic Association and the American Physical Therapy Association.

Furthermore, in most of the websites consulted, even by non-experts, the reason for the onset of spinal pain is attributed to hyperlordosis and pelvic anteversion. However, this thought is not entirely in agreement with other scientific publications. Therefore it is necessary to pay attention to online searches which often answer these questions without taking EBM into account.

None of the studies reported above take into consideration the time factor. In fact, all the studies have evaluated the immediate changes brought about by heel raising. Women who complain of lower back pain when wearing high-heeled shoes rarely experience pain as soon as they start wearing them.

The objective of the research arises from these considerations. The aim of this study (primary outcome) is to investigate whether wearing high-heeled shoes for at least 2 hours modifies the spinopelvic parameters compared to the barefoot condition and as soon as the shoes are worn.

The secondary outcome will be to verify in the sample analyzed whether there are different behaviors between the subgroups of those who have complained in their anamnesis and those who have never complained of lower back pain when using high-heeled shoes for a few hours.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

A three-dimensional analysis of the posterior surface will be performed with the Formetric 4D® rasterstereographic device (Diers International GmbH, Schlangenbad, Germany).

Participants will be given a questionnaire which investigates:

  • Age, weight, height of the participants;
  • Any pain in the spine (measured by NPS) usually reported by subjects after using high-heeled shoes;
  • Type of profession;
  • Frequency with which the subjects wear the heeled shoe (how many hours per week);
  • Heel height of the shoe with which they participate in the clinical study;
  • Any spinal pain (measured by NPS) after wearing heeled footwear for the study period.

This last data will be filled in at the end of the evaluation.

For the evaluation of the secondary outcome, on the basis of the data from the medical history sheet, the sample will be divided into two groups:

  1. The first group (group A, ASYMPTOMATIC) includes subjects who during daily life do not report spinal pain after wearing high-heeled shoes;
  2. The second group (group S, SYMPTOMATIC) is made up of participants who usually complain of more or less intense pain after using the shoe.

The subjects will be asked to bring their own pair of shoes with a heel that is at least 8.7 cm, the average height reported by the work of Schroeder and Hollander, where average height means the difference between the height of the heel and the height of the raised part at the forefoot level (plateau). A particular heel width will not be required, because it seems that the height of the heel influences muscle activation, in particular the paravertebral muscles, while the width of the heel has no significant effects on them.

Conversely, amplitude has a greater influence on balance when standing and while walking.

Three evaluation will be performed:

  1. first evaluation in neutral position with bare feet (T0)
  2. second evaluation in neutral position wearing shoes (T1);
  3. third evaluation like the previous one but at least 2 hours apart, in which it will be required to remain standing still or walk (T2).

Statistic analysis

A descriptive analysis of the population will be performed to determine the mean values and standard deviations (SD) of both the combined group and the subgroups A and S. T-tests for independent data will be used to verify whether there are any significant differences between the two subgroups .

The distribution of the data will be verified using graphical representation. If the distribution is normal (p <0.05) for the comparison between T1 vs T2 the t-test for paired data will be used and between the subgroups (T1S vs T1A and T2S vs T2A) t-test for independent data with statistical significance accepted for p values <0.05. ANOVA will be used to simultaneously compare the pre and post of both groups.

If the data does not have a normal distribution (p >0.05) the Wilcoxon test will be used for the comparison between the T1 vs T2 data of the total group and the Mann-Whitney U test for the comparison between subgroups (T1S vs T1A and T2S vs T2A). The Friedman test will be used to simultaneously compare the pre and post of both groups.

Study Type

Observational

Enrollment (Estimated)

34

Contacts and Locations

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

Study Contact

Study Contact Backup

Study Locations

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

  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Usual female users of shoes with heels at least 7 cm high, with a frequency of at least twice a week and/or less than 3 hours/week

Description

Inclusion Criteria:

  • female subjects aged between 20 and 40 years
  • Usual users of shoes with heels at least 7 cm high, with a frequency of at least twice a week and/or less than 3 hours/week

Exclusion Criteria:

  • structural or neurological anomalies that may prevent you from remaining weight-bearing, for approximately 2 hours, with shoes having a heel (difference between the heel and the plateau) of at least 7 cm high;

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
effect of high-heeled shoes on trunk inclination
Time Frame: 2 hours after wearing high heels
The aim of this study is to investigate whether wearing high-heeled shoes for at least 2 hours modifies the flexion of the antero-posterior trunk (measured as the angle between the vertical and the line that passes through the prominent cervical vertebra and the line that connects the two dimples) compared to the barefoot condition and as soon as the shoes are worn.
2 hours after wearing high heels
effect of high-heeled shoes on pelvic inclination
Time Frame: 2 hours after wearing high heels
The aim of this study is to investigate whether wearing high-heeled shoes for at least 2 hours modifies the pelvic inclination angle (the angle between the vertical and the tangent to the lumbosacral junction) compared to the barefoot condition and as soon as the shoes are worn.
2 hours after wearing high heels
effect of high-heeled shoes on lordotic angle
Time Frame: 2 hours after wearing high heels
The aim of this study is to investigate whether wearing high-heeled shoes for at least 2 hours modifies the lordotic angle (angle measured between the tangents of the thoracolumbar junction and the lumbosacral junction) compared to the barefoot condition and as soon as the shoes are worn.
2 hours after wearing high heels
effect of high-heeled shoes on kyphotic angle
Time Frame: 2 hours after wearing high heels
The aim of this study is to investigate whether wearing high-heeled shoes for at least 2 hours modifies the kyphotic angle (angle measured between the tangents of the cervicothoracic junction and the thoracolumbar junction) compared to the barefoot condition and as soon as the shoes are worn.
2 hours after wearing high heels
effect of high-heeled shoes on lumbar arrow
Time Frame: 2 hours after wearing high heels
The aim of this study is to investigate whether wearing high-heeled shoes for at least 2 hours modifies the lumbar arrow (horizontal distance in millimeters of the lumbar spine from the virtual vertical line that passes through the kyphotic apex) compared to the barefoot condition and as soon as the shoes are worn.
2 hours after wearing high heels
effect of high-heeled shoes on cervical arrow
Time Frame: 2 hours after wearing high heels
The aim of this study is to investigate whether wearing high-heeled shoes for at least 2 hours modifies the cervical arrow (horizontal distance in millimeters of the cervical spine from the virtual vertical line that passes through the kyphotic apex) compared to the barefoot condition and as soon as the shoes are worn.
2 hours after wearing high heels

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
different response on trunk inclination between the subgroups (suffering from back pain and asymptomatic)
Time Frame: 2 hours after wearing high heels
The secondary outcome will be to verify in the sample analyzed whether there are different behaviors of the flexion of the antero-posterior trunk (measured as the angle between the vertical and the line that passes through the prominent cervical vertebra and the line that connects the two dimples) between the subgroups of those who suffer from low-back pain and those who have never complained of low-back pain when using high-heeled shoes for a few hours.
2 hours after wearing high heels
different response on pelvic inclination between the subgroups (suffering from back pain and asymptomatic)
Time Frame: 2 hours after wearing high heels
The secondary outcome will be to verify in the sample analyzed whether there are different behaviors of the pelvic inclination angle (the angle between the vertical and the tangent to the lumbosacral junction) between the subgroups of those who suffer from low-back pain and those who have never complained of low-back pain when using high-heeled shoes for a few hours.
2 hours after wearing high heels
different response on lordotic angle between the subgroups (suffering from back pain and asymptomatic)
Time Frame: 2 hours after wearing high heels
The secondary outcome will be to verify in the sample analyzed whether there are different behaviors of the lordotic angle (angle measured between the tangents of the thoracolumbar junction and the lumbosacral junction) between the subgroups of those who suffer from low-back pain and those who have never complained of low-back pain when using high-heeled shoes for a few hours.
2 hours after wearing high heels
different response on kyphotic angle between the subgroups (suffering from back pain and asymptomatic)
Time Frame: 2 hours after wearing high heels
The secondary outcome will be to verify in the sample analyzed whether there are different behaviors of the kyphotic angle (angle measured between the tangents of the cervicothoracic junction and the thoracolumbar junction) between the subgroups of those who suffer from low-back pain and those who have never complained of low-back pain when using high-heeled shoes for a few hours.
2 hours after wearing high heels
different response on lumbar arrow between the subgroups (suffering from back pain and asymptomatic)
Time Frame: 2 hours after wearing high heels
The secondary outcome will be to verify in the sample analyzed whether there are different behaviors of the lumbar arrow (horizontal distance in millimeters of the lumbar spine from the virtual vertical line that passes through the kyphotic apex) between the subgroups of those who suffer from low-back pain and those who have never complained of low-back pain when using high-heeled shoes for a few hours.
2 hours after wearing high heels
different response on cervical arrow between the subgroups (suffering from back pain and asymptomatic)
Time Frame: 2 hours after wearing high heels
The secondary outcome will be to verify in the sample analyzed whether there are different behaviors of the cervical arrow (horizontal distance in millimeters of the cervical spine from the virtual vertical line that passes through the kyphotic apex) between the subgroups of those who suffer from low-back pain and those who have never complained of low-back pain when using high-heeled shoes for a few hours.
2 hours after wearing high heels

Collaborators and Investigators

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

Sponsor

Investigators

  • Principal Investigator: Saverio Colonna, MD, Spine Center

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 (Actual)

December 15, 2023

Primary Completion (Actual)

February 15, 2024

Study Completion (Estimated)

February 28, 2024

Study Registration Dates

First Submitted

February 11, 2024

First Submitted That Met QC Criteria

February 22, 2024

First Posted (Estimated)

March 1, 2024

Study Record Updates

Last Update Posted (Estimated)

March 1, 2024

Last Update Submitted That Met QC Criteria

February 22, 2024

Last Verified

February 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Heel01

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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