Introducing a Telemedicine Strategy to Deliver Cervical Cancer Screening Results in El Salvador
Telemedine
2 other identifiers
interventional
1,103
1 country
1
Brief Summary
Telemedicine, the use of telecommunication technologies to provide healthcare services remotely, has grown exponentially in the last decade. The COVID-19 pandemic highlighted the potential of these approaches as routine clinical interactions transitioned from in-person to virtual modalities around the world. While some telemedicine applications are only feasible in high-resource settings, other types have been shown to be effective in low and middle-income countries (LMICs). Interventions that utilize mobile devices such as cellular phones and digital tablets, collectively known as mobile health or mHealth, may enable greater patient access to some services and reduce the strain on resource-limited health systems. Here we describe the use of an mHealth strategy to facilitate delivery of cervical cancer screening results in El Salvador.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 31, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 31, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
January 31, 2024
CompletedFirst Submitted
Initial submission to the registry
March 16, 2026
CompletedFirst Posted
Study publicly available on registry
March 19, 2026
CompletedMarch 19, 2026
March 1, 2026
Same day
March 16, 2026
March 16, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
Proportion of results received
Proportion of women who received their results in each group
45 days
Proportion of results received
Proportion of women who received their results in each group within 45 days
45 days
Study Arms (2)
Telemedicine
ACTIVE COMPARATORReceived screening result through SMS message
Control
NO INTERVENTIONReceived screening result in person
Interventions
Women receive their screening results via SMS message instead of in person
Eligibility Criteria
You may qualify if:
- Women aged 30-59
You may not qualify if:
- No history of cervical cancer
- No HPV testing in the past 5 years
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- The Cleveland Cliniclead
- National Cancer Institute (NCI)collaborator
Study Sites (1)
Ministry of Health Clinics
San Salvador, 000000000, El Salvador
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Miriam Cremer, MD
The Cleveland Clinic
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 16, 2026
First Posted
March 19, 2026
Study Start
January 31, 2024
Primary Completion
January 31, 2024
Study Completion
January 31, 2024
Last Updated
March 19, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share