Prevent Post-discharge Hospital Admissions Using Mobile Phone App
The Role of Physician-Patient Communication Through Mobile Phone Application in Preventing Emergency Room Admissions After Circumcision: a Randomized Prospective Study
1 other identifier
observational
184
1 country
1
Brief Summary
The investigators aimed to assess the impact of a mobile phone application facilitating real-time visual and verbal communication on reducing emergency room admissions following circumcision.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Apr 2024
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2024
CompletedFirst Submitted
Initial submission to the registry
August 19, 2024
CompletedFirst Posted
Study publicly available on registry
September 19, 2024
CompletedSeptember 19, 2024
September 1, 2024
3 months
August 19, 2024
September 12, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
The Role of Physician-Patient Communication through Mobile Phone Application in Preventing Emergency Room Admissions after Circumcision: A Randomized Prospective Study
Predicting reduction in patient readmission rate using telemedicine assistance
To estimate the change in the readmission rate during the participants; recovery period (2 months)
Study Arms (2)
Communication Group
Physician-Patient Communication Group
Non-Communication Group
Physician-Patient Non-Communication Group
Interventions
Comminication via Telemedicine With Patients
Eligibility Criteria
Cases of circumcision
You may qualify if:
- Circumcision
You may not qualify if:
- hypospadias
- cryptoorchidism
- bleeding diathesis
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Cumhuriyet Univercity
Sivas, Sivas, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 3 Months
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Phd
Study Record Dates
First Submitted
August 19, 2024
First Posted
September 19, 2024
Study Start
April 1, 2024
Primary Completion
June 30, 2024
Study Completion
June 30, 2024
Last Updated
September 19, 2024
Record last verified: 2024-09
Data Sharing
- IPD Sharing
- Will not share