Home ultrasound in telemedicine care for gestational diabetes (GDM)

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This single-center randomized trial compares standard high-risk care for gestational diabetes with a care model that adds physician-guided home ultrasound during telemedicine visits. Participants will alternate in-person and telemedicine visits, using the Pulsenmore device under real-time supervision to assess fetal status. Primary outcome is patient satisfaction at term measured by the DTSQ, with secondary outcomes including glycemic control, maternal and neonatal outcomes, healthcare utilization, visit duration, and costs. The study will enroll 90 women with singleton pregnancies and GDM at Edith Wolfson Medical Center in Israel over one year.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Singleton pregnancy
* GDM diagnosed by OGTT or glucose monitoring
* Hebrew speaking
* Compatible cellphone

Exclusion Criteria:

* Pregestational diabetes
* Fetal anomalies/genetic abnormalities
* Multifetal pregnancy
* Late GDM diagnosis (after 34 weeks)

Where it's running

• Edith Wolfson Medical Center
  H̱olon, Central District, Israel Recruiting

Study contacts

• Principal investigator: LIat Mor — Edith Wolfson Medical center
• Study coordinator: Liat Mor
• Email: liatmor1@gmail.com
• Phone: +972546738294

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Other studies for the same condition or treatment. Recruiting studies are listed first.

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• Investigating how meal timing affects blood sugar during pregnancy

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.