Exploring neuroplasticity associated with a combined computerised cognitive training and psychoeducation program in patients with mild cognitive impairment and /or a lifetime history of depressio

Not Applicable

Active, not recruiting

• Conditions: Depression; mild cognitive impairment; Mental health; Mental Health - Depression

• Registration Number: ACTRN12611000570987
• Lead Sponsor: Sharon Naismith

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2011-06-03
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Active, not recruiting
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

Cognitive impairment or depression or vascular risk factors

Exclusion Criteria

Stroke, transient ischaemic attack (TIA), poor English skills, unable to attend 10-weeks of therapy, neurological disorder, dementia, psychiatric disorder, medical illness with known cognitive effects, prior head injury.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Formal neuropsychological testing will assess performance in a number of cognitive domains including learning and memory, language, speed of processing, attention and working memory, and executive functioning. <br><br>The primary outcome is memory which will be measured using the Rey Auditory Verbal Learning Test and the Logical Memory subtest of the Wechsler Memory Scale-III[Participants are assessed at trial entry, and again after 7 weeks of either 'cognitive training' or 'treatment as usual' (ie. waitlist).]