Quantifying placebo effect on psychomotor and cognitive functions in adult healthy human volunteers: an open-label, assessor-blind, cross-over randomized control study
Not Applicable
Completed
- Registration Number
- CTRI/2020/10/028474
- Lead Sponsor
- Archana
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 54
Inclusion Criteria
Healthy Participants of either gender with age 20-45 years
Education qualification of at least graduation
Participants free from any disease requiring treatment
Participants willing to give informed consent
Exclusion Criteria
Participants taken any medicine in the last 7 days
History of clinical anxiety, depressive state or any other psychiatric illness
History of visual or auditory impairment
Pregnant and lactating women
Inability to understand the given instructions
Substance abuse disorders including excessive intake of alcohol, tobacco (more than 10 cigarettes / day), coffee, tea or drinks containing caffeine (equivalent to more than 4 cups per day)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the effect of single dose placebo, on psychomotor function in healthy human volunteers when compared with no-treatment groupTimepoint: Day 4,5,6
- Secondary Outcome Measures
Name Time Method 1.To evaluate the effect of single dose placebo, on memory of healthy human volunteers when compared with no-treatment group.Timepoint: Day 4,5,6;2.To evaluate the effect of single dose placebo, on executive function of healthy human volunteers when compared with no-treatment groupTimepoint: Day 4,5,6