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Clinical Trials/ACTRN12621001168842
ACTRN12621001168842
Active, Not Recruiting
N/A

A cluster randomised, controlled trial evaluating a novel Holistic Approach in Primary care for PreventIng Memory Impairment aNd Dementia (HAPPI MIND) intervention aimed at assessing and reducing dementia risk factors as measured using the Australian National University - Alzheimer's Disease Risk Index (ANU-ADRI)

Monash University0 sites403 target enrollmentAugust 30, 2021

Overview

Phase
N/A
Intervention
Not specified
Conditions
Not specified
Sponsor
Monash University
Enrollment
403
Status
Active, Not Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 30, 2021
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Community\-dwelling adults, aged 45\-65years, with two or more modifiable risk factors for dementia who have access to, and are able to use, a smartphone, and who have had at least one visit to the practice/clinic in the previous 12 months, will be eligible. One or more visits will indicate patient engagement with the practice/clinic.
  • Modifiable risk factors include: high blood pressure, hyperlipidaemia, type 2 diabetes, obesity, current smoking, physical inactivity, poor diet, excessive drinking of alcohol, depression, social isolation and lack of cognitive stimulation.

Exclusion Criteria

  • Patients who are unable to provide informed consent, those unable to communicate in English, those with a terminal illness (anticipated survival \<36 months) or those with other conditions preventing participation in the study as judged by the GP or their nominee will be excluded. Patients with a history of existing dementia, cognitive impairment or other significant neurologic disease (e.g. Parkinson’s disease, Huntington’s disease, multiple sclerosis, normal pressure hydrocephalus, progressive supranuclear palsy, seizure disorder, subdural hematoma, or history of significant head trauma with persistent neurologic sequelae or known structural brain abnormalities) will be excluded. Patients who are involved in other clinical trials targeting any of the modifiable risk factors for dementia listed above will be excluded.

Outcomes

Primary Outcomes

Not specified

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