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A SINGLE CENTRE STUDY EVALUATING ADHERENCE TO MONITORING GUIDELINES IN PATIENTS WITH RHEUMATOID ARTHRITIS byGenevieve Olivier A minidissertation submitted in partial fulfilment of the requirements
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01
Define the research question and objectives of the study.
02
Select an appropriate study design (e.g., randomized, observational).
03
Identify the target population for the study.
04
Determine eligibility criteria for participants.
05
Develop a detailed protocol including methodology, sample size, and timeline.
06
Obtain necessary ethical approvals and consent from participants.
07
Recruit participants according to the eligibility criteria.
08
Collect data meticulously according to the study protocol.
09
Analyze the collected data using appropriate statistical methods.
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Write a report summarizing the findings, conclusions, and implications.

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Researchers looking to gather focused data on a specific group or condition.
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Organizations needing to conduct clinical trials or pilot studies.
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Healthcare providers wanting to evaluate new treatments in a controlled setting.
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Regulatory bodies requiring evidence for new interventions.
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A single centre study is a research study conducted at one specific location or institution, focusing on a defined group of participants, often used in clinical trials to evaluate the efficacy and safety of a treatment.
Researchers or institutions conducting clinical trials or medical studies that involve human subjects are typically required to file a single centre study with an appropriate regulatory body or ethics committee.
To fill out a single centre study, researchers must complete the study protocol, collect and document relevant participant information, obtain informed consent, and submit a detailed application to the ethics committee and regulatory authorities.
The purpose of a single centre study is to investigate specific research questions in a controlled environment, allowing for more straightforward data collection and management while minimizing variability from multiple sites.
Information that must be reported includes study objectives, methodology, participant demographics, ethical considerations, safety data, results of the study, and any conflicts of interest.
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