Human Factoring Validation of Pulsenmore ES Device

PulseNmore

Status: Completed

Conditions: Pregnancy Related

Treatments: Device: Pulsenmore ES home ultrasound

Study type: Observational

Funder types: Industry

Identifiers

NCT06567067

SPRIM 22-1200

Details and patient eligibility

About

The goal of this study is to conduct human factors validation testing with the Pulsenmore ES home Ultrasound device in the video-guided mode of operation (participants) and the clinician-guided mode of operation (participants and healthcare professionals (HCP)) to evaluate whether the device/user interface can be used by the intended users without any serious issues or errors under that intended use and actual use conditions. The intended users will be qualitatively assessed via observation and cognitive debrief and usability testing methodology. Participants will be remotely observed during the video-guided fetal scanning actual process and participants and HCPs will be remotely observed during the clinician-guided fetal scanning actual process.

Enrollment: 57 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria for participants:

• The participant has voluntarily provided and signed the informed consent form (ICF)
• The participant has voluntarily provided authorization and signed the Videography and Photography Release form
• The participant is able to speak, read, write and comprehend US English and resides in the United States of America
• The participant to have adequate communications skills
• Pregnant women > 18 years of age
• A singleton gestation
• Gestational age between 14 to 38 weeks with a prior scan demonstrating fetal viability and confirming dates
• Maximum BMI of 40
• Willing and able to participate in a 60-75 min video and is willing to be audio recorded for the post-procedure interview

Inclusion criteria for HCP:

• The HCP has voluntarily provided and signed the HCP consent information sheet (CIS)
• The HCP has voluntarily provided authorization and signed the HCP Videography and photography Release form
• The HCP is able to speak, read, write and comprehend US English and resides in the United States of America.
• The HCP has adequate communications skills
• The HCP is willing and able to participate in one 60 min video call and is willing to be audio recorded during the interview.

Exclusion Criteria for participants:

• Multiple gestation
• Skin problem(s) in the abdominal area (such as wounds, cuts in the skin and skin rash)
• The participant has a visual or hearing impairment, and/or a condition that affects her motor and/or cognitive skills, that would prevent her from independently performing a fetal ultrasound scan at home
• The participant has a language barrier that can affect the communication and compliance to the usability study requirement
• Uncontrolled and untreated psychiatric conditions for a minimum of 6 months prior to screening,
• Alcohol or drug dependence with current symptoms
• Previous Pulsenmore ES trials and have previously used the Pulsenmore ES device
• Known fetal and genetic anomalies.

Exclusion criteria for clinicians:

• The HCP has a visual or hearing impairment, that would prevent him or her from independently directing a fetal ultrasound scan
• The HCP has a language barrier and/or in the opinion of the recruiting interviewer provides any reason to believe that compliance with the study requirements will not be achievable
• The HCP has participated in in previous Pulsenmore trials and have previously used the Pulsenmore ES device

Trial design

57 participants in 2 patient groups

Video guided

Description:

Participants will perform a scan using Pulsenmore ES device in the video mode independently following video tutorial. Participants will be remotely observed during the scan and interviewed by a human factoring researcher right after

Treatment:

Device: Pulsenmore ES home ultrasound

Clinician guided

Description:

Participants will perform a scan using Pulsenmore ES device either in the clinician guided mode, guided by a health care professional via a telehealth visit. Participants and healthcare professionals will be remotely observed during the scan and interviewed by a human factoring researcher right after

Treatment:

Device: Pulsenmore ES home ultrasound