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Randomized CONTROLLED TRIAL TO ASSESS THE CLINICAL AND COSTEFFECTIVENESS OF PHYSIOTHERAPY AND OCCUPATIONAL THERAPY IN PARKINSON IS DISEASEACRONYM: PD RETRIAL PROTOCOL VERSION 9New REC Ref 08/H1211/168
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How to fill out randomised controlled trial to
01
To fill out a randomised controlled trial (RCT), follow these steps:
02
Design the research question and hypothesis: Clearly state the question you want to answer with your trial and formulate a hypothesis.
03
Determine the eligibility criteria: Define the characteristics that participants must have to be included in the trial.
04
Randomly assign participants to groups: Randomly allocate participants to either the treatment group or the control group.
05
Interventions or exposures: Clearly describe the interventions or exposures that participants in each group will receive.
06
Outcome measures: Clearly define the primary and secondary outcomes that will be measured in the trial.
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Data collection: Determine the methods and instruments that will be used to collect data from participants.
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Sample size calculation: Calculate the required sample size using appropriate statistical methods.
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Ethics approval and informed consent: Obtain ethical approval for the trial and ensure that participants give informed consent to participate.
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Conduct the trial: Implement the trial according to the designed protocol and collect the data.
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Data analysis: Analyze the collected data using statistical methods to determine if there are significant differences between the treatment and control groups.
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- Regulatory bodies: RCTs are used to assess the safety and effectiveness of medical interventions before they are approved for use.
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- Patients and the general public: RCTs contribute to improving healthcare and finding better treatments for diseases.
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What is randomised controlled trial to?
Randomised controlled trial is a research design that uses randomisation to allocate participants into different groups for comparison.
Who is required to file randomised controlled trial to?
Researchers conducting clinical trials or studies requiring randomisation are required to file randomised controlled trial forms.
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Randomised controlled trial forms can be filled out electronically or on paper, following the specific guidelines and instructions provided by the regulatory authorities.
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The purpose of randomised controlled trial is to ensure unbiased and scientifically valid results by randomly assigning participants to different treatment groups.
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Randomised controlled trial forms typically require information on study design, participant demographics, interventions, outcomes, and statistical analyses.
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