The chronic effects of Bacopa on cognitive performance in Alzheimer's patients - A pilot study
- Conditions
- Alzheimer's diseaseNeurological - Alzheimer's diseaseAlternative 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- Withdrawn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
Diagnosis of mild to moderate Alzheimer's disease
Aged 60 and above
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
Name Time Method 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
Name Time Method 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]