Innovative, Midlife Intervention for Dementia Deterrence: Feasibility Randomized Controlled Trial

Completed

• Conditions: Dementia; 10012272

• Registration Number: NL-OMON42204
• Lead Sponsor: niversiteit Maastricht

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2016-01-06
• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 144

Inclusion Criteria

-Registered with a participating general practice
-Age 40 - 60 on date of consent
-Presence of any one (or more) of the following risk factors:
o Depression - previous history or active episode of minor depression as recorded on medical record - if GP deems patient fit to participate
o Diabetes (diagnosis e.g. on a diabetes disease register)
o Hypertension
o Obesity (BMI >= 30)
o Current smoker
o High cholesterol
o Coronary heart disease (diagnosis e.g. on a coronary heart disease register)
o Self-reported sedentary lifestyle
o Self-reported lack of cognitive stimulation
- Medically stable
-Proficient in Dutch language
-Access to internet in order to communicate by email and access information online

Exclusion Criteria

-Active episode of major depression, if GP deems patient too severely ill to participate, recorded in medical record or assessed by a validated instrument
-People who are unable to give informed consent
-People who have dementia

Study & Design

• Study Type: Interventional
• Study Design: Not specified