The effectiveness of an online cognitive intervention program ('Houd uw brein vitaal') in healthy adults, a randomized controlled trial

Completed

• Conditions: geen aandoeningen; gezonde cognitieve veroudering; healthy cognitive aging

• Registration Number: NL-OMON38981
• Lead Sponsor: niversiteit Maastricht

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2014-03-15
• Last Update Posted: 11 June 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 375

Inclusion Criteria

* signed informed consent
* age between 40 and 65 years old
* adequate comprehension of the Dutch language
* availability of desktop or laptop computer

Exclusion Criteria

* history of chronic neurological or neurodegenerative disorders (e.g. stroke or dementia)
* abuse of alcohol and/or drugs

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The primary study parameters are subjective cognitive functioning (memory<br /><br>self-efficacy, self evaluation, and everyday mistakes).</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>The secondary study objectives are objective cognitive functioning (measured<br /><br>with 3 different cognitive tasks) and psychological wellbeing (measured with<br /><br>questionnaires).</p><br>