- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07742618
Effectiveness of AI-Assisted Clinical Documentation
Effectiveness of AI-Assisted Clinical Documentation: Evidence From a Staggered Rollout at the Western Uusimaa Wellbeing Services County
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Laura Jernström, PhD
- Phone Number: +358413629767
- Email: laura.jernstrom@utu.fi
Study Locations
-
-
-
Turku, Finland
- University of Turku
-
Contact:
- Laura Jernström, PhD
- Phone Number: +358413629767
- Email: laura.jernstrom@utu.fi
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Member of study population: nurses working at wellchild or student health care services of Western-Uusimaa Wellbeing Services County.
Exclusion Criteria:
- Nurse works in several teams.
- Under 18 years.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Sequential Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Early-Treated
Nurses adopting AI clinical documentation tool (treatment)
|
AI clinical documentation tool is adopted starting at different assigned time points by eight subgroups.
Early vs later adopters are compared using staggered difference-in-differences design.
The order of subgroups is randomized for 7/8 subgroups.
|
|
Experimental: Later-Treated
Nurses that have not yet adopted AI clinical documentation tool (control)
|
AI clinical documentation tool is adopted starting at different assigned time points by eight subgroups.
Early vs later adopters are compared using staggered difference-in-differences design.
The order of subgroups is randomized for 7/8 subgroups.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Ratio of completed statutory health check-ups
Time Frame: 7 months.
|
7 months.
|
|
|
Number of completed statutory health check-ups
Time Frame: 7 months.
|
7 months.
|
|
|
Working Hours
Time Frame: 7 months.
|
Number of working hours (average and dynamic measures)
|
7 months.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Time use
Time Frame: 7 months.
|
Questionnaire. Time used in documentation and other tasks (self-assessed). "How much time did you spend on each activity during the preceding workday (on average per client)?
|
7 months.
|
|
Job Satisfaction
Time Frame: 7 months.
|
Questionnaire:
Very dissatisfied Fairly dissatisfied Neither dissatisfied nor satisfied Fairly satisfied Very satisfied |
7 months.
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
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
Other Study ID Numbers
- TY/1110/2026
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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