Alerting on adverse Drug reactions: Falls prevention Improvement through developing a Computerized clinical support system: Effectiveness of Individualized medicaTion withdrawal

Recruiting

• Conditions: Vallen met letsel; falls with injury; Injurious falls

• Registration Number: NL-OMON51926
• Lead Sponsor: Academisch Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 9 April 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 856

Inclusion Criteria

1. 65 years or older;
2. history of a fall (in the past year);
3. a Mini-Mental State Examination Score of 21 points or higher or a Montreal
Cognitive Assessment - Dutch score of 16 points or higher;
4. willingness to sign informed consent;
5. Use of at least one FRID; and
6. sufficient command of the Dutch language.

Exclusion Criteria

1. Life expectancy of less than one year;
2. Immobility (bedridden, e.g. inability to walk short distances with
assistance of a walking aid)

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The main study parameter is the time to the first injurious fall. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary outcome measures are: number of injurious falls, time to first fall<br /><br>resulting in minor injuries, number of falls resulting in minor injuries, time<br /><br>to first fall, total number of falls, (health-related) quality of life, and<br /><br>patient-reported outcomes. We will also conduct a process evaluation to<br /><br>evaluate the implementation of the CDSS and patient portal and we will<br /><br>investigate the cost-effectiveness of the CDSS and patient portal</p><br>