Biomechanical Effects of Wearing a Sacroiliac Belt in Women

NCT ID: NCT03334799

Last Updated: 2017-11-07

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

Clinical Phase

NA

Total Enrollment

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-02-25

Study Completion Date

2017-09-09

Brief Summary

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Women with pelvic girdle pain PGP) often get relief from using a sacroiliac belt. The study will explore if there are differences and in the changes of lower body movement in stability with the belt on and with the belt off. Women with PGP will be matched with women without to explore if there is a difference between these two groups. This will be looked at in standing and in walking.

Detailed Description

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SacroIliac (SI) joint dysfunction (also called pelvic girdle pain) has been associated with impaired load transfer across the lumbopelvic region. This can result in lower back pain as well as poor biomechanical adaptation during walking. Sacroiliac (SI) belts have typically been prescribed in order to mitigate pain and improve load transfer in individuals with SI joint dysfunction. It has been speculated that SI belts have the ability to instantaneously increase joint stability, and as a result improve load transfer and muscle activation and recruitment. However, this speculation is primarily based on anecdotal evidence; there is little biomechanical research supporting the effects of wearing an SI belt. In order to gain an improved understanding of the biomechanical effects of wearing an SI belt, the investigators propose to conduct a study with the following key objectives:

1. Determine if there are differences with respect to neuromuscular, kinematic, or pressure patterns during walking and/or standing between healthy stable individuals and individuals with SI joint dysfunction
2. Determine if wearing an SI belt affects neuromuscular, kinematic, or pressure patterns during walking and/or standing in women with sacroiliac instability

Variables measured will include:

1. Kinematics will be collected to quantify posture and joint angles
2. Kinetics will be collected to quantify ground reaction forces
3. Plantar pressure will be collected to quantify force distribution and center or pressure
4. Joint moments (Lumbar-pelvic and Hip) will be added as variables. The investigators will use inverse dynamics to calculate various joint moments during walking.

Conditions

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Pelvic Girdle Pain

Keywords

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sacroiliac belt kinematics stability pelvic girdle pain sacroiliac instability

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

case control
Primary Study Purpose

SCREENING

Blinding Strategy

NONE

Study Groups

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Sacroiliac belt on and off

Belt on and belt off

Group Type OTHER

sacroiliac belt

Intervention Type DEVICE

standing and walking with the belt on and with the belt off

Interventions

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sacroiliac belt

standing and walking with the belt on and with the belt off

Intervention Type DEVICE

Other Intervention Names

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pelvic belt

Eligibility Criteria

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Inclusion Criteria

* Females
* Individuals with isolated SI joint dysfunction
* Individuals with shoe size 6, 7, 8 or 9 US

and matched controls by age (within 5 years), BMI (within one point) and parity

Exclusion Criteria

* Pregnancy in the last year or presently pregnant
* Significant lumbar dysfunction
* Significant hip dysfunction
* Leg length discrepancy of 1 cm or more
* Women who have previously undergone prolotherapy or SI joint injections
* Women with previous lower back, hip, knee or ankle surgery
* Inability to stand for 60 sec unaided or to walk unaided.
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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University of Calgary

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Magali Robert

Role: PRINCIPAL_INVESTIGATOR

Foothils Hospital Cumming School of Medicine

Other Identifiers

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14-2323

Identifier Type: -

Identifier Source: org_study_id