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This document serves as the participant information leaflet and informed consent form for a clinical trial conducted by Morinaga Milk Industry, assessing the effect of Bifidobacterial Supplementation on bowel movements in healthy adults aged 18 to 65 with constipation. The study is randomized, double-blinded, and placebo-controlled, involving monitoring, questionnaires, health checks, and the consumption of either a probiotic supplement or placebo over an eight-week period. Participants will...
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01
Begin by gathering all necessary personal information, including your full name, date of birth, and contact details.
02
Provide relevant demographic information such as gender, ethnicity, and health status as required.
03
Complete the section regarding your involvement in the study, including any relevant medical history.
04
If applicable, describe any medications you are currently taking.
05
Review the consent section carefully and make sure you understand your rights as a participant.
06
Sign and date the document where indicated to confirm your participation.

Who needs afcro-171 participant information leaflet?

01
Anyone participating in a study or clinical trial that requires consent and personal information documentation needs the afcro-171 participant information leaflet.
02
Researchers and clinical trial coordinators who are obligated to inform participants of the study details and data handling requirements also need it.
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The afcro-171 participant information leaflet is a document that provides essential information regarding the participation in a specific program or study, detailing rights, responsibilities, and relevant procedures.
Researchers, organizations, or individuals conducting studies or programs that require participant consent are required to file the afcro-171 participant information leaflet.
To fill out the afcro-171 participant information leaflet, follow the instructions provided in the document, including entering participant details, study information, and consent statements as required.
The purpose of the afcro-171 participant information leaflet is to inform participants about the study's goals, procedures, potential risks, benefits, and their rights, ensuring informed consent.
The afcro-171 participant information leaflet must report information such as the study's purpose, duration, procedures, risks, benefits, compensation details, and the contact information of the researchers.
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informed consent clinical trial probiotic supplementation bowel movements constipation randomized study placebo-controlled health monitoring participant information Morinaga Milk Industry

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