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PARTICIPANT INFORMATION SHEET AND CONSENT FORM STUDY INFORMATION Protocol Title: A randomized controlled trial of electroacupuncture in the management of patients with axial Spondyloarthritis in Singapore

How to fill out a randomized controlled trial

How to fill out a randomized controlled trial

1. To fill out a randomized controlled trial, follow these steps:
2. Identify the research question or problem that you want to investigate.
3. Design a study protocol that outlines the objectives, study population, inclusion and exclusion criteria, interventions, and outcome measures.
4. Obtain ethical approval from the relevant research ethics committee.
5. Determine the sample size required for your study by conducting a power analysis.
6. Randomly assign participants to either the intervention group or the control group. This can be done using computer-generated randomization sequences or random number tables.
7. Implement the interventions or treatments according to the study protocol.
8. Collect data on the outcome measures from both the intervention and control groups.
9. Analyze the data using appropriate statistical methods.
10. Interpret the results and draw conclusions based on the findings.
11. Report the trial findings in a scientific paper following the guidelines for publishing randomized controlled trials.

Who needs a randomized controlled trial?

1. Randomized controlled trials are needed by researchers, scientists, and healthcare professionals who want to evaluate the efficacy and safety of interventions or treatments.
2. Pharmaceutical companies often conduct randomized controlled trials to gather evidence for regulatory approval of new drugs.
3. Government agencies may require randomized controlled trials to inform policy decisions related to healthcare interventions.
4. Medical practitioners may utilize randomized controlled trials to make evidence-based treatment recommendations.
5. Patients can also benefit from randomized controlled trials as they provide reliable evidence to guide medical decision-making and improve patient outcomes.

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What is a randomized controlled trial?

A randomized controlled trial (RCT) is a type of scientific experiment that aims to reduce bias when testing a new treatment or intervention. Participants are randomly assigned to either the treatment group or the control group, allowing researchers to compare outcomes between the two groups.

Who is required to file a randomized controlled trial?

Researchers, organizations, or institutions that are conducting clinical trials involving new treatments or interventions are typically required to file a randomized controlled trial.

How to fill out a randomized controlled trial?

Filling out a randomized controlled trial typically involves submitting a comprehensive trial protocol that includes details such as the study design, objectives, methodology, participant criteria, and ethical considerations, often through a clinical trial registry or regulatory body.

What is the purpose of a randomized controlled trial?

The purpose of a randomized controlled trial is to evaluate the effectiveness and safety of a treatment or intervention by comparing results between participants who receive the treatment and those who do not, minimizing other variables that could affect the outcome.

What information must be reported on a randomized controlled trial?

Key information that must be reported includes the trial's title, objectives, methodology, participant demographics, outcomes assessed, statistical analysis plan, and results, including any adverse events.