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Pragmatic Randomized controlled trial of a TraumaFocused Guided Self Help Program versus Individual TraumaFocused Cognitive Behavioral Therapy for Post-traumatic Stress Disorder (RAPID)PROTOCOL Sponsor: Sponsor
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Identify the research question or objective for the pragmatic randomised controlled trial.
02
Determine the target population or study sample for the trial.
03
Develop the eligibility criteria for participants to be included in the trial.
04
Randomly assign participants to one of the trial groups.
05
Implement the interventions or treatments being tested in each trial group.
06
Collect data and information from the participants regarding the outcomes of interest.
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Analyze the data collected and assess the effects of the interventions or treatments.
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Interpret the results of the trial and draw conclusions based on the findings.
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Report the findings of the trial in a clear and transparent manner following relevant guidelines and standards.

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Pragmatic randomised controlled trials are needed by researchers, healthcare professionals, and policymakers.
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Researchers can use these trials to evaluate the effectiveness and real-world impact of interventions or treatments.
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A pragmatic randomised controlled trial is a type of study design that evaluates the effectiveness of an intervention in real-world settings.
Researchers and scientists conducting clinical trials are required to file pragmatic randomised controlled trials.
To fill out a pragmatic randomised controlled trial, researchers must carefully design their study protocol, obtain ethical approval, recruit participants, collect data, and analyze the results.
The purpose of pragmatic randomised controlled trials is to provide evidence on the effectiveness of interventions in real-world conditions, to inform clinical decision-making.
Researchers must report on the study design, methodology, participant characteristics, intervention details, outcomes measured, results, and conclusions.
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