Posturography Changes During Pregnancy

C

Caps Research Network

Status

Completed

Conditions

Pregnant Women

Treatments

Diagnostic Test: Anthropometrics
Diagnostic Test: Vitals
Other: Health and daily activity questionnaires
Diagnostic Test: Posturography Evaluation

Study type

Observational

Funder types

Other

Identifiers

NCT03067116
CI-IRB-20160524-01

Details and patient eligibility

About

Determine balance changes during pregnancy

Full description

The subjects will be tested at enrollment and during weeks 20, 24, 28, 32, 36, 40 of their pregnancy, as well every 4 weeks postpartum up to 6 months. The following protocol will be used: Subjects will also be asked to answer a short health questionnaire. The following data will be recorded each time: height, minimum stance width, circumference measurements of the chest, abdomen, hip and each thigh as well as a supine fundal height. A full body side-profile photo was also taken to determine the curvature of the spine. A session questionnaire will be used to determine if the subject had fallen or noticed any changes in their daily activity. In a seated position, the following measurements will be recorded: 1-minute heart rate variability (HRV) with paced breathing, temporal scan body temperature, respiration rate, heart rate, blood pressure and SpO2 (these last three will be measured bilaterally). Subject will undergo posturography testing using the modified Clinical Testing of Sensory Integration in Balance (mCTSIB) protocol: four 30 s tests in the following conditions: eyes open on a rigid surface (NSEO), eyes closed on a rigid surface (NSEC), eyes open on a compliant surface (PSEO), and eyes closed on a compliant surface (PSEC). At the end of the posturography testing, heart rate, blood pressure and SpO2 will be re-measured bilaterally in the standing and then seated positions, as will be the seated HRV.

Enrollment

4 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

healthy women less than 20 weeks pregnant

Exclusion criteria

women affected by any pathology and/or more than 20 weeks pregnant

Trial design

4 participants in 1 patient group

Subjects
Description:
Adult, healthy pregnant women undergoing Posturography Evaluation, Anthropometrics, Vitals and answering Health and daily activity questionnaires
Treatment:
Diagnostic Test: Posturography Evaluation
Other: Health and daily activity questionnaires
Diagnostic Test: Vitals
Diagnostic Test: Anthropometrics

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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