Skip to content

Feasibility of Point-of-Care Ultrasound Training and Remote Quality Assurance for Community Physicians in Conflict-Affected Syria

Feasibility of Point-of-Care Ultrasound Training and Remote Quality Assurance for Community Physicians in Conflict-Affected Syria

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07677553
Enrollment
9
Registered
2026-07-01
Start date
2026-01-01
Completion date
2026-08-31
Last updated
2026-07-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Training

Brief summary

Background: POCUS can extend diagnostic capabilities where conventional imaging is unavailable, yet evidence on its implementation in active conflict zones remains scarce. We describe the feasibility of a POCUS training, device deployment, and remote quality assurance program for community physicians working in village clinics in Syria. Methods: Nine physicians from five community clinics participated in a two-day in-person POCUS training course adapted to a conflict-affected, resource-constrained setting. The curriculum focused on cardiac, lung, FAST, and soft-tissue applications. At course completion, each clinic received a handheld Butterfly ultrasound device. Participants subsequently uploaded examinations to a cloud-based platform for remote expert review and feedback. Outcomes included immediate post-course satisfaction, perceived confidence, and early post-course POCUS use over follow-up.

Interventions

OTHERTraining in POCUS

Training in point of care ultrasound

Sponsors

Meir Medical Center
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years

Inclusion criteria

Nine physicians from five community clinics serving villages in a region of Syria that cannot be further specified for security reasons participated in the program. Participants represented several medical specialties and were selected in collaboration with IFA based on their involvement in frontline community care and their anticipated ability to integrate POCUS into clinical practice. \-

Exclusion criteria

None \-

Design outcomes

Primary

MeasureTime frameDescription
immediate post-course satisfactionImmediately after the completion of the courseImmediately after the course, all nine participants completed a feedback questionnaire assessing course delivery, instructor quality, content, hands-on practice, perceived confidence, and anticipated clinical utility

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 2, 2026