Planning¶
Syllabus mapping
Working Scientifically outcome — Planning. Covers identifying and managing variables, designing a fair and valid method, assessing risk, and selecting appropriate equipment. Like every Working Scientifically outcome, it's assessed through application inside a focus area's practicals and depth study, not as standalone content.
Exact NESA outcome code TODO — confirm against the official syllabus PDF (Resources) before treating any wording on this page as verbatim NESA text.
You need to know: how to name your three types of variables correctly, how to design a method that actually isolates the relationship you're testing, and how to fill out a risk assessment properly — not just as a formality.
Core¶
The three types of variable¶
Every fair investigation in this course has (at minimum) these three:
- Independent variable (IV) — the one thing you deliberately change between trials.
- Dependent variable (DV) — the thing you measure, which you expect to respond to the IV.
- Controlled variables — everything else that could affect the DV, which you deliberately hold constant so the only thing changing is the IV.
Worked example
Investigation: how the angle of an inclined plane affects a trolley's acceleration (see Questioning and Predicting).
| Variable | Role | This investigation |
|---|---|---|
| Angle of incline | Independent | Deliberately set to 10°, 20°, 30°, 40°, 50° |
| Acceleration | Dependent | Measured via light gates or a motion sensor at each angle |
| Trolley mass | Controlled | Same trolley used for every trial |
| Surface of the ramp | Controlled | Same ramp material throughout (affects friction) |
| Release method | Controlled | Trolley released from rest, not pushed, every time |
A method that changes the angle and swaps trolleys partway through hasn't isolated anything — if the acceleration changes, you can't tell whether it was the angle or the trolley. This is the whole point of "fair testing": change one thing, measure one thing, hold everything else still.
Fair testing vs a control¶
Two related but different ideas get called "control" in science:
- Controlled variables (above) — the things you deliberately keep the same across every trial of a single experiment.
- A control experiment (or control group) — a separate, baseline trial run with no treatment applied, used as a comparison point. This shows up constantly in biology and medicine (a placebo group, an untreated sample) but is less common in a typical Year 11 physics prac, where you're usually comparing a range of IV values against each other rather than against a no-treatment baseline. It's still worth knowing the distinction, since "control" gets used loosely and command-verb questions sometimes expect you to be precise about which one you mean.
Designing the method itself¶
A few things worth deciding before you're standing at the bench, not while you're there:
- Range of the independent variable — spread values across a sensible range (not clustered at one end), so a resulting graph actually shows a trend rather than a cluster of nearby points.
- Number of data points — enough IV values to draw a convincing line or curve; five or six is a reasonable minimum for a Year 11 prac unless told otherwise.
- Repeats — plan to repeat each trial (typically 3+) so you can calculate a mean and get a sense of how consistent your results are. This matters for Conducting and becomes essential once you get to processing uncertainty.
- Equipment precision — pick equipment whose precision actually matches what you're trying to detect. A ruler with mm markings can't meaningfully distinguish a 0.3 mm difference; a stopwatch operated by hand has a reaction-time uncertainty of roughly 0.2–0.3 s regardless of how many decimal places it displays.
Risk assessment¶
A risk assessment isn't a box-ticking formality — it's how you show you thought about what could go wrong before it does. NESA (and every school's WHS policy) expects one to accompany any practical involving equipment, chemicals, electricity, heat, or moving parts.
The standard structure:
| Hazard | Risk | Likelihood | Consequence | Control |
|---|---|---|---|---|
| What could cause harm | What could actually happen | How likely, given your setup | How bad if it happens | What you'll do to reduce it |
Worked example — electromagnet prac
From Magnetism's suggested prac (factors affecting electromagnet strength):
| Hazard | Risk | Likelihood | Consequence | Control |
|---|---|---|---|---|
| Current-carrying wire/coil | Wire overheating with sustained high current | Medium (depends on current used and duration) | Minor burn | Use current within the power supply's rated limit; switch off between trials rather than leaving it energised continuously |
| Iron/steel core and nail | Sharp point on the nail | Low | Minor puncture/scratch | Handle by the shaft, not the point; store point-down when not in use |
| Power supply | Electric shock from exposed terminals | Low (low-voltage DC supply) | Minor shock | Check cable insulation before use; switch off before adjusting connections |
Note the pattern: every hazard gets a specific, actionable control — not "be careful," which controls nothing.
Advanced
Pilot studies. Before committing to a full run of trials, a short pilot (one or two quick trials across the planned IV range) can reveal problems a plan alone won't — an IV range that's too narrow to show a trend, a DV that's too small to measure reliably with the chosen equipment, or a control that turns out to be harder to hold constant than expected. Adjusting the method after a pilot, and explicitly saying so in a report, is good practice, not a sign the original plan was bad — it's evidence of exactly the kind of iterative refinement Working Scientifically as a whole is trying to develop.
Extension
Beyond the Physics 11–12 syllabus — won't appear in the HSC, included for interest / depth study inspiration.
📎 Depth study idea
Clinical and pharmaceutical trials take the "control" idea much further than a typical physics prac does, using a control group that receives no treatment (or a placebo) and comparing it against a treatment group — often blinded (the participant doesn't know which group they're in) or double-blinded (neither the participant nor the person administering the treatment knows, to eliminate bias from expectation). There's a genuine, if less obvious, physics-adjacent parallel: any investigation involving human measurement — reaction-time-based timing, judging a "just noticeable" light or sound intensity — inherits the same expectation bias problem trials are designed to control for. Worth a depth study if you're investigating anything where a human is part of the measurement chain, not just the equipment.
Video/visual resources¶
- 🎥 Khan Academy — TODO: source a variables / experimental design explainer. Must define IV/DV/controlled clearly with a worked example, and ideally cover why equipment precision matters (matching the stopwatch-vs-light-gate point above). Essential.
- 🎥 Physics High — TODO: unlikely to have a generic risk-assessment/variables video — more realistic to skip this line, or link a specific NSW school WHS risk assessment template/guide instead of a video.
Check yourself¶
-
For an investigation into how the number of turns in a coil affects the strength of an electromagnet (see Magnetism), identify the independent variable, the dependent variable, and two controlled variables.
Answer
Independent: number of turns in the coil. Dependent: electromagnet strength (e.g. number of paperclips lifted, or a field sensor reading). Controlled (any two): current supplied, core material, wire gauge/thickness, distance between the electromagnet and whatever it's picking up.
-
Explain why a hand-held stopwatch is a poor choice of equipment for measuring the very short time it takes a trolley to cross a 20 cm light-gate interval, even though the stopwatch displays results to 0.01 s.
Answer
The stopwatch's displayed precision (0.01 s) is misleading — the actual limiting factor is human reaction time when starting/stopping it, which is roughly 0.2–0.3 s. For a very short interval, that reaction-time uncertainty could be a large fraction of (or even larger than) the time being measured, making the result unreliable regardless of how many decimal places are shown. A light gate, which starts/stops electronically without human reaction time in the loop, is far more appropriate.
-
Write a two-row risk assessment (Hazard, Risk, Likelihood, Consequence, Control) for an investigation into refractive index using a glass block and a ray-box light source (see Wave Behaviours).
Answer
Example (answers will reasonably vary):
Hazard Risk Likelihood Consequence Control Bright ray-box light source Eye discomfort from staring directly into the beam Low Temporary glare, minor discomfort Avoid looking directly into the beam; view the ray's path on the paper, not the source Glass block Cuts from a chipped/broken edge Low Minor cut Inspect the block before use; handle by the flat faces, not the edges