Effects of Palmaria palmata on dyslipidemia and psychological stress - Randomized, double-blind, placebo-controlled parallel-group comparative study

INTERVENTION: Administration of placebo twice daily for 8 weeks Administration of Palmaria palmata (2g/day) twice daily for 8 weeks CONDITION: Dyslipidemia PRIMARY OUTCOME: LDL cholesterol INCLUSION CRITERIA: 1)Participants who are 20‐year‐old or older, and younger than 60‐year‐old at the time of obtaining informed consent 2)Participants whose fasting serum LDL colesterol levels are more than 120 mg/dL 3)Participants who can visit the medical institution according to schedule 4)Participants who are able to understand the study and willing to provide written informed consent