Actively Recruiting

Age: 18Years - 40Years
FEMALE
ID06471790

Movement Observation and Tracking In Obstetrics - Epidural and Ambulation Feasibility Study Using Inertial Sensors

Led by Hospices Civils de Lyon · Updated on 2026-01-20

30

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying the use of wearable inertial sensors to monitor movement and gait during the first stage of labor, focusing on pregnant women using low-dose epidural analgesia that allows walking. The study aims to better understand the biomechanical changes and gait characteristics affected by labor, pain, fetal progression, and epidural analgesia. This feasibility study explores how these sensors could help track analgesia effectiveness, predict fall risks, and analyze labor progression. Participants will be pregnant women in labor who receive walking epidural analgesia according to the current service protocol. They will be monitored continuously from the first stage of labor until delivery using wearable inertial sensors that capture triaxial velocity changes. The sensors provide real-time, non-invasive data on walking movements during labor. During the study, researchers will measure detailed gait changes starting from when participants request epidural analgesia until delivery. Data will include velocity changes over time captured by the sensors. Participants will be observed without intervention beyond normal care, allowing for assessment of movement patterns and potential safety concerns. The study will help validate this technology for future obstetrical monitoring.

CONDITIONS

Brief Title

Inertial Sensors for Obstetrical Walking Epidural Tracking

Who Can Participate

Age: 18Years - 40Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Pregnancy at or beyond 38 weeks gestation
  • No significant medical history (American Society of Anesthesiologists class ASA 1)
  • Receiving low-dose epidural analgesia with ambulation according to current service protocol
  • Willingness to participate in the study
Not Eligible

You will not qualify if you...

  • Refusal to participate in the study
  • Non-French-speaking patient
  • History of osteoarticular problems affecting gait (such as severe scoliosis, spinal surgery, congenital hip deformity, pelvic fracture, ligament or knee joint issues)
  • Adults under legal protection
  • Multiple pregnancy
  • Need for continuous intravenous infusion with infusion stand during ambulation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Monitoring

Duration - From first stage of labor until delivery

Participants who receive walking epidural analgesia during labor will be monitored using inertial wearable sensors from the first stage of labor until delivery.

Continuous monitoring during labor

Trial Site Locations

Total: 1 location

1

Hôpital de la Croix Rousse

Lyon, France, 69004

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Research Team

M

Mikhail DZIADZKO, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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