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The chronic effects of Bacopa on cognitive performance in Alzheimer's patients - A pilot study

Phase 4
Withdrawn
Conditions
Alzheimer's disease
Neurological - Alzheimer's disease
Alternative and Complementary Medicine - Other alternative and complementary medicine
Registration Number
ACTRN12612000785808
Lead Sponsor
Swinburne University of Technology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Withdrawn
Sex
All
Target Recruitment
40
Inclusion Criteria

Diagnosis of mild to moderate Alzheimer's disease
Aged 60 and above

Exclusion Criteria

less than 60 years of age
History of, or current psychiatric illness
Neurological diseases (other than Alzheimers)
Suffering from Endocrine, gastrointestinal or bleeding disorders
A history of chronic illness or infection
Pregnant or lactating
current use of medications including; anticoagulants, antidepressants, anti-psychotics, anxyolitics, anti-parkinsons.
current use of illicit drugs, cognitive enhancing drugs, or vitamin and herbal supplements

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Cognitive performance - score on the Alzheimer's Disease Assessment Scale- Cognition (ADAS-COG)[baseline and 90 days after intervention commencement];Cognitive performance - Mini Mental State Examination (MMSE) score[baseline and 90 days after intervention commencement];Performance on Cognitive Drug Research (CDR) computerised test battery[baseline and 90 days after intervention commencement]
Secondary Outcome Measures
NameTimeMethod
Mood, as measured by the Visual Analog Mood Sclaes (VAMS)[baseline and 90 days after intervention commencement];Quality of life, as measure by Cornell-Brown Scale for Quality of life in Dementia, and the Assessment of Quality of Life.[baseline, 30, 60 and 90 days after intervention commencement];Cognitive performance - Swinburne Computerised Cogntiive Assessment Battery (SUCCAB)[baseline and 90 days after intervention commencement];mean response time on an Inspection time task[baseline and 90 days after intervention commencement]
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