Breastfeeding — Feasibility and Effectiveness of WhatsApp Online Group on Breastfeeding by Peer Counsellors.
Citation(s)
Ahmad N, Shariff ZM, Mukhtar F, Lye MS Family-based intervention using face-to-face sessions and social media to improve Malay primary school children's adiposity: a randomized controlled field trial of the Malaysian REDUCE programme. Nutr J. 2018 Aug 2;17(1):74. doi: 10.1186/s12937-018-0379-1.
Department of Health Breastfeeding Survey 2019. Available from: https://www.fhs.gov.hk/english/archive/files/reports/BF_survey_2019.pdf.
Lau Y, Htun TP, Tam WS, Klainin-Yobas P Efficacy of e-technologies in improving breastfeeding outcomes among perinatal women: a meta-analysis. Matern Child Nutr. 2016 Jul;12(3):381-401. doi: 10.1111/mcn.12202. Epub 2015 Jul 21. Review.
Premji S Mobile health in maternal and newborn care: fuzzy logic. Int J Environ Res Public Health. 2014 Jun;11(6):6494-503.
Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.
Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.
Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.
Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.
Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.