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Prevention of Dementia in Older Adults- Tiruvalla Interventional Study in Ageing

Not Applicable
Conditions
Health Condition 1: F028- Dementia in other diseases classified elsewhere
Registration Number
CTRI/2023/11/060181
Lead Sponsor
IH
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Individuals between 60-75 years old, willing to participate and comply with all the study evaluation and intervention procedures

CAIDE (Cardiovascular Risk Factors, Aging and Dementia) Dementia Risk Score of 6 points or higher

Mini Mental State Examination, MMSE <26 and >20

Exclusion Criteria

Barthel index < 90.

Geriatric Depression Scale = 9

Dementia or Moderate Cognitive impairment (MMSE < 20).

Disorders that may affect safe involvement in the intervention (eg, malignancy, symptomatic cardiovascular disease, Large vessel stroke in the past two years, History of transient ischemia attack (TIA) or small vessel stroke in the last 6 months, revascularisation within 1 year previously, severe loss of vision, hearing, or communicative ability)

Coincident participation in another intervention trial.

Recent ( < 3 months) bone fracture.

History of hip fracture, joint replacement, or spinal surgery in the last 6 months

Clinically significant abnormalities in laboratory blood tests as per the judgment of the site study clinician.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Cognitive ability will be assessed using Addenbrookes cognitive examinationTimepoint: Cognitive ability will be assessed at baseline, 6 months, 12 months and 24 months.
Secondary Outcome Measures
NameTimeMethod
Depresiion, quality of life , ADLTimepoint: <br/ ><br>measurements will be made at baseline, 12 months & 24 months
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