- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06761105
Using Anonymous Data From A Digital Tool for Medical History-Taking To Improve Healthcare Services
Observation Of The Use Of Digital Tools for Medical History-Taking in Primary Care and Utilization of Anonymous Routine Data for Health Services Research
This study aims to understand how people use a mobile app that helps them record their symptoms before going to the doctor. Patients use the app on a tablet or other digital device. The app guides patients through a series of structured questions tailored to their symptoms. The data collected is then transferred to the practice's electronic record and is available to the treating doctor before and during the consultation.
In this project, anonymized usage data will be analyzed to contribute to the further development of the tool and to provide valuable insights for health services research.
Study Overview
Status
Conditions
Detailed Description
In several studies the usability of digital medical history tools has been demonstrated. These tools allow acute complaints to be recorded using an app before a medical consultation and the data collected to be transferred to the electronic medical record.
The aim of the study is to investigate the effectiveness and use of a digital medical history tool that is becoming increasingly popular in general practice. To this end, it is aimed to evaluate anonymized usage data provided by the company that distributes the app, aidminutes gUG, as part of an observational study with the aim of identifying potential for further development and for questions of health services research (e.g. on the frequency of GP consultations, morbidity and frequency of complaints). This is a retrospective data analysis of anonymous routine data in a cross-sectional design.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Frank Müller, MD PhD
- Phone Number: +495513965663
- Email: frank.mueller@med.uni-goettingen.de
Study Contact Backup
- Name: Eva Maria Noack
- Phone Number: +495513965745
- Email: evamaria.noack@med.uni-goettingen.de
Study Locations
-
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Lower Saxony
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Göttingen, Lower Saxony, Germany, 37073
- Recruiting
- Department of General Practice
-
Contact:
- Frank Müller, MD PhD
- Phone Number: +495513965663
- Email: frank.mueller@med.uni-goettingen.de
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- all patients that use the app in a general practice that agreed to provide data
- all ages (including children if the app is used by parent or legal guardian)
- all complaints chosen in the app
Exclusion Criteria:
- patients that use the app in a general practice that did not agree to provide data
- patients that use the app in a general practice outside of the federal state Lower Saxony
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Patients
Patients who have used the digital medical history tool in one of the participating general practices
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Use patterns
Time Frame: From enrollment to the end of app use, up to 8 years
|
Evaluation of the use patterns and frequencies of the medical history tool
|
From enrollment to the end of app use, up to 8 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Data quality
Time Frame: From enrollment to the end of app use, up to 8 years
|
Investigation of the consistency and completeness of the medical history data collected by the medical history tool
|
From enrollment to the end of app use, up to 8 years
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 4/8/24
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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