Effect of Krill Oil on Cognitive Function in Adults
- Conditions
- Subjective Memory Impairment
- Interventions
- Dietary Supplement: Placebo groupDietary Supplement: Krill oil group
- Registration Number
- NCT04347421
- Lead Sponsor
- Pusan National University Yangsan Hospital
- Brief Summary
The investigators conduct a randomized, double-blind, placebo-controlled study to investigate the effects of Krill oil on cognitive function in adults with subjective memory impairment for 12 weeks.
- Detailed Description
Previous animal studies have indicated that Krill oil may have the ability to improve cognitive function. Therefore, the investigators conduct a randomized, double-blind, placebo-controlled study to investigate the effects of Krill oil on cognitive function in adults with subjective memory impairment for 12 weeks; the safety of the compound are also evaluate. The Investigators examine chemical and metabolic parameters, and cognitive function at baseline, as well as after 6 and 12 weeks of intervention. One hundred adults were administered either 500 mg of Krill oil or a placebo each day for 12 weeks.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 100
- Global Deterioration Scale (GDS) 2 or 3
- Abnormal liver or renal function (i.e., serum aminotransferase activity > 3 times of upper limit of reference range and serum creatinine concentrations > 1.2 mg/dL)
- Diabetes (diagnosed clinically or fasting glucose level > 126 mg/dL)
- History of viral hepatitis or cancer
- Uncontrolled hypertension
- History of serious cardiac disease such as angina or myocardial infarction
- History of gastrectomy
- History of medication for psychiatric disease
- Administration of oriental medicine including herbs within the past 4 weeks
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Placebo group Placebo group This group takes Placebo for 12 weeks Krill oil group Krill oil group This group takes Krill oil for 12 weeks
- Primary Outcome Measures
Name Time Method Mini-Mental State Examination total score Change from Baseline Mini-Mental State Examination total score at 3 months Change in Mini-Mental State Examination total score during 3 months
- Secondary Outcome Measures
Name Time Method Korean instrumental activity of daily living total score Change in Korean instrumental activity of daily living total score during 3 months Change in Korean instrumental activity of daily living total score during 3 months
Computerized NeuroCognitive Function test total score Change in Computerized NeuroCognitive Function test total score during 3 months Change in Computerized NeuroCognitive Function test total score during 3 months
brain derived neurotrophic factor Change in brain derived neurotrophic factor level during 3 months Change in brain derived neurotrophic factor level during 3 months
Trial Locations
- Locations (1)
Pusan National University Yangsan Hospital
🇰🇷Yangsan, Gyeungsangnam-do, Korea, Republic of