A follow-up study of the Discontinuation of ANtihypertensive treatment in the Elderly (DANTE) study Leide

Completed

• Conditions: depressie, apathie, dagelijks functioneren en kwaliteit van leven; Blood pressure and cognition; 10007963; 10012272

• Registration Number: NL-OMON43484
• Lead Sponsor: eids Universitair Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 250

Inclusion Criteria

This is a follow-up study of the DANTE study Leiden. Therefore, inclusion criteria are:
(1) previous participation in the DANTE study Leiden.
(2) agreement on the informed consent form of the DANTE study Leiden that the subject may be contacted for future studies associated with the DANTE study Leiden.
(3) a confirmation of the subjects* general practitioner that the subject is able to participate in the follow-up study.

Exclusion Criteria

Judgement by the subject*s general practitioner that the subject is not able to participate in the follow-up study

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The main study parameters are blood pressure, (domains of) cognitive<br /><br>functioning, symptoms of depression and apathy, general daily functioning and<br /><br>quality of life. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary study parameters are antihypertensive medications, occurrence of<br /><br>(cardiovascular) events, as well as (new) medical diseases such as dementia,<br /><br>and death.</p><br>