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  3. Research design

Research design

How to write the Research design of the IB Biology IA: a focused research question in context, explained variables and controls, sufficient data and a specific risk assessment.

  • IB Biology
  • Internal assessment
  • SL and HL

16 min readLast reviewed 14 Oct 2026

Research design is the first of the four criteria of the scientific investigation. It assesses the research question and the scientific context it sits in, the decisions made in planning the method, and whether the method is written in enough detail for another person to repeat it.

A strong research design does most of the work for the other three criteria. If the variables are well chosen and well controlled, and enough data are collected, the analysis is straightforward, the conclusion is clear and the evaluation can focus on genuine limitations instead of avoidable mistakes.

What the criterion rewards

The descriptors look at three things: how the research question is set in context, how the methodological considerations are handled, and how complete the description of the method is. The command term changes from band to band, and the table paraphrases the difference.

Aspect

Band 1–2

Band 3–4

Band 5–6

Research question and context

The question is stated, with little or no context

The question is outlined within a broad context

The question is described within a specific and appropriate context

Methodological considerations (variables, data sufficiency, safety, ethics, environment)

Stated: listed without reasons

Described: some detail on what was done

Explained: what was done, how, and why each decision matters to the results

Description of the method

Lacks the detail needed to repeat it

Has some detail but with omissions

Detailed enough for the investigation to be reproduced

Methodological considerations are every decision that affects the quality of the data: the choice of measuring method and instrument, the range and spacing of the independent variable, the number of repeats, the controlled variables, preliminary trials, and safety, ethical and environmental issues. The top band needs reasons for each of these, not only a list.

Exam tip

Moderators look for the word "because" in a research design. "The volume of hydrogen peroxide was kept at 10.0 cm³" is a description. "The volume of hydrogen peroxide was kept at 10.0 cm³ with a pipette (±0.05 cm³), because the amount of substrate available affects the rate of oxygen release" is an explanation.

The research question and its context

Writing the research question

The research question is one sentence that names the independent variable with its range, the dependent variable with how it is measured, and the organism or system, with its scientific name. For a correlation study, it names the two variables and the population or site. Choosing and sharpening a question is covered in "The scientific investigation"; the Research design criterion then asks how well the question is placed in its context.

Background theory tied to the variables

The context is the biology that explains why the independent variable should affect the dependent variable in the system chosen, and it is specific to those two variables and that system. For an investigation of temperature and catalase, the context covers the reaction catalysed, how temperature affects the frequency of collisions between enzyme and substrate, why the rate falls above the optimum when the enzyme undergoes denaturation, and why catalase is found in potato tuber cells. It does not need a history of enzyme research or a description of every factor that affects enzymes.

  • Explain the mechanism that links the two variables, with the key terms of the course.

  • Give the biological relevance: why the process matters in the organism (catalase protects cells from hydrogen peroxide, a toxic by-product of metabolism).

  • Cite the sources of this information in the text.

  • Where published values exist (an optimum temperature, a water potential, a typical stomatal density), mention them, because the conclusion will be compared with them.

A hypothesis is not compulsory, but a prediction with a reason drawn from the theory shows that the context has been understood. "The rate of oxygen release will increase from 20 °C to an optimum near 40 °C, then decrease sharply, because catalase is denatured at higher temperatures" is a testable prediction based on theory.

Common mistake

Writing three pages of textbook theory about enzymes in general. Background that is not linked to the two variables uses words without earning credit. Keep to the theory needed to predict and later explain the relationship being tested, usually 300–500 words.

YouTube
Walk-through of the Research design criterion of the 2025 IB Biology internal assessment: the research question, context, methodology and controls.

Variables: what is changed, measured and kept constant

Every investigation has three kinds of variable. Each is named in the report together with how it is measured or controlled, its units and the uncertainty of the instrument used.

  • The independent variable is the one changed deliberately. State its values (the range and the increments) and how each value is set and checked, for example "water bath set to each temperature and checked with a thermometer (±0.5 °C)".

  • The dependent variable is the one measured. State exactly what is measured, with which instrument, over what time, and how it is turned into the quantity analysed (for example volume of oxygen in 60 s, used as the rate in cm³ min⁻¹).

  • The controlled variables are the other factors that could affect the dependent variable. For each, state the value used, how it was kept constant, and why it matters.

The "why" is where most marks are lost. A controlled variable matters because it would change the dependent variable if it varied, which would make it impossible to say whether a change in the results was caused by the independent variable. Explaining the mechanism for each one (more substrate means more collisions per second) turns a list into an explanation.

Controlled variable

Value

How it is controlled

Why it matters

Concentration of hydrogen peroxide

3%

Same stock solution used for every trial, stored in the dark

A higher substrate concentration increases the frequency of enzyme–substrate collisions and the rate

Volume of hydrogen peroxide

10.0 cm³

Measured with a 10 cm³ pipette (±0.05 cm³)

Determines the total amount of substrate available

Surface area of potato tissue

5 discs, 10 mm diameter, 2 mm thick

Cut with a size 6 cork borer and a scalpel against a 2 mm template

Only catalase in cells at or near the cut surface reacts quickly; more surface area means more enzyme in contact with substrate

Source of potato tissue

One tuber

All discs cut from the same tuber on the same day

Catalase content differs between tubers and changes with storage

pH

pH 7.0

2.0 cm³ of phosphate buffer added to each flask

pH changes the shape of the active site and the rate

Time of collection

60 s

Stopwatch started when the bung is inserted

Volume collected depends on how long the reaction runs

Time at the set temperature before mixing

5 min

Discs and hydrogen peroxide equilibrated separately in the water bath

Ensures both are at the set temperature when the reaction starts

Variables that cannot be controlled

In fieldwork and in studies of people, many variables cannot be held constant. Light intensity, soil moisture and temperature change during a field day; the age, fitness and diet of participants differ. These are monitored instead: measured and recorded, so that their possible effect can be discussed in the evaluation. Choosing sites, times or participants that are as similar as possible limits their influence. A variable that changes along with the independent variable and could explain the results is a confounding variable, and the design should try to remove or measure it.

Tip

For each controlled variable, ask "if this changed between trials, what would happen to my dependent variable, and why?" If you can answer, you have the explanation for the table. If you cannot, the variable may not matter enough to include.

Choosing and justifying the method

The method is the procedure used to set the independent variable and measure the dependent variable. Justifying it means explaining why that method and instrument were chosen over the alternatives, usually because they give more precise, more objective or more relevant data.

Catalase activity can be measured in several ways: by counting bubbles, by timing how long a filter-paper disc soaked in catalase takes to rise through hydrogen peroxide, by measuring the height of foam, or by collecting the oxygen in a gas syringe or an inverted measuring cylinder. Counting bubbles is quick but bubbles vary in size. A gas syringe measures the volume of oxygen directly, to ±0.5 cm³, and is the most precise of these methods for a school laboratory. The diagram of the apparatus shows the set-up chosen for the sample investigation.

A conical flask containing 10.0 cm³ of 3% H₂O₂ with pH 7 buffer and 5 potato discs stands in a water bath with a thermometer (±0.5 °C). A bung and delivery tube carry the O₂ released to a horizontal gas syringe (100 cm³, ±0.5 cm³).A conical flask containing 10.0 cm³ of 3% H₂O₂ with pH 7 buffer and 5 potato discs stands in a water bath with a thermometer (±0.5 °C). A bung and delivery tube carry the O₂ released to a horizontal gas syringe (100 cm³, ±0.5 cm³).
The flask sits in a water bath so that the reaction runs at the set temperature, and the gas syringe collects all the oxygen released. Labels give the instrument uncertainties that belong in the method.

Preliminary trials

Preliminary trials are small-scale runs of the method before the real data are collected. They show whether the method works and set values that would otherwise be guesses. In the catalase investigation, trials might show that at 40 °C about 19 cm³ of oxygen is collected in 60 s, a volume well within the 100 cm³ scale and large compared with the ±0.5 cm³ uncertainty, so 60 s is a suitable collection time; or that discs float and stick to the side of the flask unless the flask is swirled once. Reporting what the trials showed and what was changed as a result is strong evidence of explained methodological considerations.

Worked example

In a pilot of an osmosis investigation, a student finds that sweet potato cylinders left in sucrose solutions for 30 minutes change in mass by less than 0.02 g, only twice the 0.01 g resolution of the balance. Suggest two changes to the method based on this result and explain each.

Show the solution

The change in mass is too small compared with the uncertainty of the balance, so the method cannot detect differences between the solutions.

  • Leave the cylinders in the solutions for longer (for example 24 hours, covered to prevent evaporation). More time allows more water to move by osmosis, so the change in mass becomes much larger than ±0.01 g.

  • Use a balance with a resolution of 0.001 g, or thinner discs of tissue. A finer balance reduces the uncertainty; thinner discs have a larger surface area to volume ratio, so water moves in or out faster.

Both changes make the measured effect large compared with its uncertainty. The preliminary trial revealed the problem before the real data were collected.

Sufficiency of data

Sufficient data means enough levels of the independent variable, over a wide enough range, with enough repeats, to answer the research question with confidence. A useful rule is at least five levels and at least five repeats at each level, but the right numbers depend on the question.

Decision

What to consider

Catalase example

Range

Wide enough to show the whole relationship, including any optimum, plateau or threshold

20–60 °C covers the rise, the optimum and the fall from denaturation

Increments

Evenly spaced, with closer spacing where the result changes fastest or an important point is expected

10 °C steps, with extra levels at 35 and 45 °C around the expected optimum (7 levels)

Repeats

Enough to calculate a mean and standard deviation and to identify anomalous results

5 repeats at each temperature (35 trials in total)

Sample size (field or human studies)

Enough quadrats, organisms or participants to represent the population and support a statistical test

Not applicable; in a transect study, for example, at least 10 quadrats per site

Repeats allow the mean and the standard deviation to be calculated, so the variation in the data can be measured and a statistical test can be carried out. Three repeats are rarely enough for a meaningful standard deviation. The number of trials possible in the time available sets a limit, so there is usually a trade-off between more levels and more repeats. Explaining that trade-off is itself a methodological consideration.

number of trials=levels×repeats=7×5=35number of trials=levels×repeats=7×5=35

A total of 35 trials at about 8 minutes each (setting up, equilibrating, collecting, cleaning) takes roughly 4.5 hours, which fits within two or three laboratory sessions. Collecting all the data with one batch of potato and one stock of hydrogen peroxide also keeps those variables constant.

Common mistake

Testing only three levels of the independent variable, such as 20, 40 and 60 °C. Three points cannot show the shape of a curve or locate an optimum: the optimum could be anywhere between 20 and 60 °C. Use at least five levels, with closer spacing where the change is expected.

Safety, ethics and the environment

Definition

Risk assessment: an evaluation of the hazards in a method, the likelihood and severity of harm from each, and the precautions taken to reduce the risk to people, other organisms and the environment.

A good risk assessment is specific to the method. It names each hazard, says what harm it could cause and gives the precaution. A table is the clearest way to present it and does not use up the word count.

Hazard

Risk

Precaution

Hydrogen peroxide (3%)

Irritant to eyes and skin

Safety glasses and gloves worn; spills diluted and wiped up with water

Water bath at up to 60 °C

Scalds

Flasks handled with tongs; bath not overfilled

Scalpel and cork borer

Cuts

Tissue cut on a tile, cutting away from the body; blade sheathed when not in use

Glassware

Cuts from breakage

Flasks checked for cracks; broken glass placed in the glass bin

Disposal

Environmental impact

Dilute hydrogen peroxide poured down the sink with plenty of water; potato tissue composted

Ethical considerations come under the same criterion. An investigation on potato tissue raises no ethical issues, and saying so in one sentence is enough. An investigation on animals or people must follow the IB animal experimentation policy and obtain informed consent, as described in "The scientific investigation". The environmental impact includes disposal of chemicals and, in fieldwork, trampling, removing organisms and leaving the site as it was found.

A worked example: a full research design

The sample investigation tests the effect of temperature on the rate of catalase activity in potato tuber. The write-up in the worked example shows the level of detail and explanation expected in the top band. It is shorter than a real report, which would also include the full background theory and citations, but every section is present.

Worked example

Write the research design section for an investigation of the effect of temperature on the rate of catalase activity in potato tuber (Solanum tuberosum). Include the research question, the context, the variables, the method, data sufficiency and the risk assessment.

Show a model write-up

Research question. What is the effect of temperature (20, 30, 35, 40, 45, 50 and 60 °C) on the rate of catalase activity in potato tuber (Solanum tuberosum), measured as the volume of oxygen released from 10.0 cm³ of 3% hydrogen peroxide in 60 s?

Context. Catalase is an enzyme found in the peroxisomes of most aerobic cells, including the storage cells of potato tubers. It breaks down hydrogen peroxide, a toxic by-product of metabolism, into water and oxygen: 2H₂O₂ → 2H₂O + O₂. As temperature rises, enzyme and substrate molecules have more kinetic energy, so they collide more often and the rate of reaction increases. Above the optimum, increased vibration breaks the hydrogen bonds and other interactions that hold the tertiary structure, the active site changes shape and the enzyme is denatured, so the rate falls. Crude potato catalase has been reported to have maximum activity at about 40 °C (Taha, 2016). The volume of oxygen released in a fixed time is directly proportional to the number of substrate molecules broken down, so it measures the rate.

Hypothesis. The rate of oxygen release will increase from 20 °C to a maximum near 40 °C and then decrease, falling steeply by 60 °C, because catalase is denatured above its optimum.

Variables. Independent: temperature, set with a thermostatic water bath and checked with a thermometer (±0.5 °C). Dependent: volume of oxygen collected in a 100 cm³ gas syringe (±0.5 cm³) in 60 s, recorded as the rate in cm³ min⁻¹. Controlled: as in the table of controlled variables (hydrogen peroxide concentration and volume, surface area and source of tissue, pH, collection time and equilibration time), each with how and why.

Method.

  1. Cut cylinders from one potato tuber with a size 6 cork borer (10 mm diameter), then cut 35 sets of five discs, each 2 mm thick, with a scalpel against a 2 mm template. Keep the discs in a covered Petri dish on damp filter paper.

  2. Set the water bath to the first temperature. Pipette 10.0 cm³ of 3% hydrogen peroxide and 2.0 cm³ of pH 7.0 phosphate buffer into a 100 cm³ conical flask and place it in the bath with one set of five discs in a boiling tube beside it. Leave both for 5 min, and check the temperature of the flask contents with the thermometer.

  3. Check the gas syringe reads 0 cm³ and is connected to the bung and delivery tube. Tip the discs into the flask, insert the bung at once and start the stopwatch.

  4. After 60 s, read the volume of oxygen on the syringe to the nearest 0.5 cm³. Record any observations (foaming, discs floating).

  5. Empty and rinse the flask with distilled water. Repeat steps 2–4 four more times at the same temperature, then for each of the other six temperatures, in a random order of temperatures to spread any drift in the potato's activity over time.

Sufficiency of data. Seven temperatures cover the expected rise, optimum and fall, with 5 °C steps around the expected optimum. Five repeats at each allow a mean and standard deviation to be calculated and a t-test between neighbouring temperatures. A preliminary trial at 40 °C collected 19 cm³ in 60 s, which is well within the 100 cm³ scale and much larger than the ±0.5 cm³ uncertainty.

Safety, ethics and environment. Hydrogen peroxide is an eye and skin irritant: safety glasses and gloves were worn. Flasks at up to 60 °C were handled with tongs. Discs were cut on a tile, away from the body. No animals or human participants were involved, so there were no ethical issues. Used hydrogen peroxide was diluted with water before disposal, and potato waste was composted.

Every decision is given with its reason, the instruments have their uncertainties, and a reader could repeat the method from these steps alone. These are the features of the top band.

The order of temperatures in step 5 is randomised for a specific reason: potato discs left waiting for an hour may lose activity as they dry or as cells are damaged. Running all the 20 °C trials first and all the 60 °C trials last would mix the effect of temperature with the effect of waiting time. Randomising spreads that effect across all temperatures.

Common mistakes and how to avoid them

  • Missing quantities. "Some hydrogen peroxide was added to potato" cannot be repeated. Give every concentration, volume, mass, size, time and temperature, with units.

  • Controlled variables listed but not explained. Give how and why for each, ideally in a table.

  • No instrument uncertainties. State the uncertainty of every measuring instrument in the method or the apparatus list.

  • Generic safety. Name the hazards specific to the method.

  • No scientific name. Name organisms and tissues precisely the first time they appear.

  • Method written as a story. Numbered steps in the order they are done are easier to follow and repeat.

Common mistake

Changing the method halfway through data collection without saying so, for example switching to a new potato or a fresh bottle of hydrogen peroxide. This introduces a variable that is not controlled. If a change was unavoidable, record when it happened and discuss its possible effect in the evaluation.

Tip

Before you finish, give your method to a classmate who has not seen your investigation and ask them to list every question they would need to ask to repeat it. Each question is a missing detail.

Reproducibility is central to science. Other scientists can test a published result only if the method is described fully, and results that cannot be reproduced are treated with caution. The same standard is applied to the method in the report.

Tip

Improve your notes. Take one practical you have done in class (for example the osmosis practical in D2.3 or the photosynthesis practical in C1.3) and rewrite its method to the top-band standard: a table of controlled variables with how and why, instrument uncertainties, justified range and repeats, and a specific risk assessment.

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