2 Seminar One
In the lecture this week
2.1 Task 1
Assessment launch
2.1.1 Instructions
- As part of your module content you will plan and conduct a pilot study
- You will individually produce an academic infographic to communicate the findings of the pilot study at a simulated conference
- You will have 20 minutes to individually present the hypothesis, methodological features and data analysis of the pilot study
2.1.2 Further guidance
- Based on previously published work you will design and conduct a pilot study based on an area of personal interest
- You will need to prepare a study protocol in accordance with good reporting guidelines and demonstrate ethical considerations (risk assessments, participant documentation, competency checks etc.)
- You will need to formulate a null and alternate hypothesis
- In planning the trial, you will need to think carefully about the methodological features used (CRABS)
- Identify the most appropriate statistical test and perform data analysis
- Using the template provided, design an academic infographic that accurately communicates the findings
- Study materials such as cue cards are permitted in this assessment
2.2 Task 2
2.2.1 Formulating a research question
The goal of this task is to develop an effective research questions for a Randomized Controlled Trial (RCT) through a structured brainstorming
2.2.2 Step One
Separate a piece of paper into four sections; modules, career, general interest, supervisor
- Modules:
- Under the “Modules” section, list your favorite or strongest performing modules.
- Beneath each module, identify and write down the specific components of the module that captivated your interest the most.
- Career:
- Under the “Career” section, list the area of employment you are interested in pursuing (e.g., clinical, pitchside, postgraduate courses).
- Identify the most contemporary or current topics within that career field.
- General Interest:
- In the “General Interest” section, write out specific topics within the field that interest you the most (e.g., kinesiotaping, ergogenic aids, variable resistance training, mobilizations).
- Supervisors:
- Under the “Supervisors” section, list your two preferred supervisors.
- For each supervisor, detail the areas in which they are experts or have research interests.
2.3 Task 3
Review your notes and identify if there are any common themes/intersections or if these themes can be woven into a cohesive research question.
2.4 Task 4
In the context of a Randomized Controlled Trial (RCT), the PICOS framework is a helpful tool for formulating a well-defined and focused research question. PICOS stands for:
- Population (P):
- Define the characteristics of the population or participants that will be included in the study.
- Specify any relevant demographic information, such as age, gender, health status, or other relevant factors.
- Intervention (I):
- Clearly describe the intervention or treatment being studied.
- Specify the key elements of the intervention, including its dosage, frequency, and duration.
- Comparison (C):
- Identify the comparison group against which the intervention will be evaluated.
- This could be a placebo, standard care, or an alternative intervention.
- Outcome (O):
- Define the primary and secondary outcomes that will be measured to assess the effectiveness of the intervention.
- Outcomes should be specific, measurable, and relevant to the research question.
- Study Design (S):
- Specify the study design, with a focus on the randomized controlled trial aspect.
- Indicate if it’s a parallel group design, a crossover design, or any other relevant design feature.
2.4.1 Characteristics of a Good RCT Question using PICOS:
- Clarity and Precision:
- The question should be clear and specific, leaving no ambiguity about the population, intervention, comparison, outcomes, and study design.
- Feasibility:
- The question should be feasible in terms of participant recruitment, intervention implementation, and data collection.
- Relevance:
- The research question should address a clinically or socially relevant issue, ensuring that the results have practical implications.
- Ethical Considerations:
- The study should adhere to ethical principles, ensuring the well-being and rights of participants.
- Measurability:
- Outcomes should be measurable and objectively assessable to provide reliable and valid results.
- Generalizability:
- Consider the external validity of the study by ensuring that the population and conditions studied are representative of the target population.
- Scientific Rigor:
- The study design, including randomization and control groups, should be robust to minimize biases and confounding factors.
- Reproducibility:
- The study should be designed in a way that allows other researchers to replicate it, contributing to the overall reliability of scientific knowledge.
Here’s an example of a research question using the PICOS framework:
In adult patients (P) with type 2 diabetes, does a structured physical activity intervention (I) compared to standard care (C) result in a significant reduction in HbA1c levels (O) over a 12-week period, as assessed in a parallel-group randomized controlled trial (S)?