None listed
Conditions
Interventions
Intervention1: Multicomponent intervention for improving cognitive function among diabetic older adults: This is 12 week multicomponent intervention with 24 sessions 2 per week. The intervention cons
Sponsors
Indian Council of Medical Research ICMR
Eligibility
Inclusion criteria
Inclusion criteria: Adults of either gender aged 60 to 70 years With diagnosis of type II diabetes for 5 or more years Education 8th grade and above With MoCA score between 18 to 25 Able to provide written consent
Exclusion criteria
Exclusion criteria: Pre existing cognitive conditions such as dementia and Alzheimer Known vascular complications of diabetes such as coronary artery disease stroke nephropathy retinopathy and polyneuropathy and other which may have compromised the physical integrity of the patient. Other chronic diseases or medical condition restricting physical exercise. Unable to understand Marathi English Subjects who have undergone or currently enrolled in a regimen of physical exercise Patients with psychiatric disorders or on medication example sedatives antipsychotics etc that are known to affect memory and psychomotor functions.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The trial will study the effectiveness of a non-drug intervention in improving cognitive and everyday functions in older adults with diabetes. It will assess changes in attention, memory, processing speed, executive function, and global cognition. The intervention s impact on cognitive capacities will be evaluated before and after its implementation.Timepoint: Cognitive test using MOCA, Wechsler Adult intelligence scale WAIS will be used to measure attention, processing speed. Trail making will be used to measure executive functioning at baseline before the start of the intervention, at 13th week after the completion of the intervention and at 6 months post intervention. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes include changes inHbA1C levels, daily living activities scores and change in depression scores.Timepoint: HbA1C levels, functionality and depression will be measured at baseline before the intervention, at 13th week immediately after the intervention and at 6 months post intervention | — |
Countries
India
Contacts
Public ContactAarti Nagarkar
Savitribai Phule Pune University
Outcome results
None listed