Author-reviewedEvidence: highv1.0.1

Conjoint Analysis

Conjoint analysis is a family of stated preference methods estimating how people value treatment or service attributes from ratings, rankings or choices.

Download concept guide
Last reviewed byDr Darrin Baines

Concept Architecture

Conjoint Analysis with Ratings, Rankings, Choices and Part-Worths in Health Preference Research

Conjoint analysis turns judgements about whole profiles, such as two ways of running a clinic, into a value for each feature that makes up the profile. In health economics it puts numbers on aspects of care outside standard health outcomes, such as waiting time or place of treatment, and it has been tested as a source of outcome weights in health technology assessment. Studies use one of three task formats (ratings, rankings and choices) and an additive part-worth model, from which relative importance and trade-offs follow, and an illustrative worked example later uses regression on ratings. Whether discrete choice experiments belong in the same family remains debated. Choice tasks have their own page on choice-based conjoint.

From conjoint measurement to a preference method

Conjoint analysis began in mathematical psychology and passed through marketing to health care. Hauser and Rao trace it to work on conjoint measurement by Luce and Tukey in 1964 and by Krantz and colleagues in 1971, who were exploring the behavioural axioms, such as additivity and independence, under which an overall judgement can be decomposed into parts. According to Hauser and Rao, Green and Rao adapted that theory to marketing and product development in 1971. Green and Srinivasan later defined conjoint analysis as any decompositional method that estimates the structure of a person's preferences, such as part-worths or importance weights, from overall evaluations of alternatives described by attribute levels.

Ryan and Farrar described its arrival in health care during the 1990s to elicit patients' and the community's views, on the premise that a service's value depends on the levels of its characteristics. An ISPOR task force report by Hauber and colleagues notes that early health applications quantified process utility and that later ones turned to patient preferences for health status, treatments and tests.

Ratings, rankings and choices as three ways to elicit preferences

All conjoint studies show respondents profiles built from attributes and levels, usually selected by an experimental design, but differ in the task. The ISPOR statistical methods report describes conjoint analysis as a broad term for methods in which respondents rate, rank or choose among such profiles, and the ISPOR checklist asks whether the format (rating, ranking or choice) suited the research question and whether it should allow for indifference.

FormatRespondent taskTypical estimationOutput
Ratings-basedScores each profile on a scaleMultiple regression on dummy-coded levelsPart-worths on the rating scale
Ranking-basedOrders profiles by preferenceNonmetric methods such as LINMAP or MONANOVA; or ranks expanded into implied choices for a logit modelInterval-scale part-worths fitted to ordinal judgements
Choice-basedPicks one profile from each setLogit or probit modelsPreference weights on a latent utility scale

The table follows Green and Srinivasan's framework, which pairs measurement scales with metric, nonmetric and choice-probability estimation; Louviere, Flynn and Carson note that rank orders can be expanded into implied choices. Ryan and Farrar reported that ranking had not yet been used in health care and that the choice approach was preferred because choices more closely resemble real decisions; choice tasks are covered on the discrete choice experiment page. Self-explicated, hybrid and adaptive methods, which ask respondents to value attributes directly, are not solely decompositional.

The part-worth model and how it is estimated

Most conjoint studies assume that the overall value of a profile is the sum of the values of its attribute levels. Each of these values is a part-worth utility. With ratings treated as an interval scale, the additive model can be estimated by linear regression as follows.

Rj=β0+∑k=1K∑l=1Lkβkl xjkl+ejR_j = \beta_0 + \sum_{k=1}^{K} \sum_{l=1}^{L_k} \beta_{kl} \, x_{jkl} + e_j

where RjR_j is the rating of profile jj, β0\beta_0 is the intercept (the predicted rating of a reference profile), βkl\beta_{kl} is the part-worth of level ll of attribute kk, xjklx_{jkl} equals 1 if profile jj shows that level and 0 otherwise, KK is the number of attributes, LkL_k the number of levels of attribute kk and eje_j the residual. One level of each attribute is the reference, with a part-worth of zero. The terms other than eje_j give the profile's overall value under the additive model.

Green and Srinivasan describe the part-worth function as more general than the vector (linear) and ideal point (linear plus quadratic) models, at the cost of more parameters, and Hauser and Rao note that regression needs at least as many observations as parameters. Ryan and Farrar, analysing choices, used a random effects ordered probit model.

The additive form rests on preferential independence, meaning that the trade-off between two attributes must not depend on the levels of the others. Hauser and Rao point out that an orthogonal main-effects design implicitly assumes this and cannot estimate interactions, so any interaction effect has to be planned at the design stage.

Relative importance and trade-offs

Part-worths have no natural unit, so studies report quantities that compare them. The ISPOR statistical report measures an attribute's importance as the difference between the part-worths of its most and least preferred levels, over the range of levels in the study. Here that range is expressed as a share of the total, as follows.

RIk=max⁡lβkl−min⁡lβkl∑h=1K(max⁡lβhl−min⁡lβhl)RI_k = \frac{\max_l \beta_{kl} - \min_l \beta_{kl}}{\sum_{h=1}^{K} \left( \max_l \beta_{hl} - \min_l \beta_{hl} \right)}

where RIkRI_k is the relative importance of attribute kk, the numerator is the range of its part-worths and the denominator sums the ranges of all KK attributes.

The ratio of two part-worths gives a marginal rate of substitution. If attribute bb is continuous, the change in bb that offsets a one-unit change in attribute aa is given below.

Δxb=−βaβb\Delta x_b = -\frac{\beta_a}{\beta_b}

where Δxb\Delta x_b is the offsetting change in bb, and βa\beta_a and βb\beta_b are the part-worths of one-unit changes in aa and bb. With cost as bb, the ratio is read as willingness to pay, but it is a welfare measure only for choice data analysed under random utility theory; Louviere, Flynn and Carson describe its use in rating-based studies as ad hoc. Ryan and Farrar used waiting time instead of cost. The 73 consistent traders retained from 157 completed questionnaires would accept about 1.3 extra months of waiting (0.77 divided by 0.59) for a local first orthodontic appointment rather than one in hospital.

Worked example of ratings-based part-worths for an outpatient clinic

The figures are hypothetical. A health board redesigning a follow-up clinic uses three two-level attributes, namely waiting time (4 or 12 weeks), location (hospital or local) and clinic lead (consultant or specialist nurse). The full factorial gives eight profiles, which one patient rates from 0 to 10. Coding is W=1W = 1 for a 12-week wait, L=1L = 1 for a local clinic and N=1N = 1 for a nurse-led clinic, and 0 otherwise.

ProfileWaitLocationLed byRating
14 weeksHospitalConsultant6
212 weeksHospitalConsultant3
34 weeksLocalConsultant8
412 weeksLocalConsultant4
54 weeksHospitalNurse5
612 weeksHospitalNurse2
74 weeksLocalNurse6
812 weeksLocalNurse4

1. Estimate the part-worths. In a balanced orthogonal design each least-squares coefficient equals the difference in mean ratings between the two levels of its attribute, as follows.

β^W=RˉW=1−RˉW=0=3.25−6.25=−3.00\hat{\beta}_W = \bar{R}_{W=1} - \bar{R}_{W=0} = 3.25 - 6.25 = -3.00

where RˉW=1\bar{R}_{W=1} is the mean rating of the 12-week profiles, (3 + 4 + 2 + 4) / 4, and RˉW=0\bar{R}_{W=0} that of the 4-week profiles, (6 + 8 + 5 + 6) / 4. Likewise the local clinic part-worth is 5.50 minus 4.00, or +1.50, and the nurse-led part-worth is 4.25 minus 5.25, or -1.00. The mean rating is 4.75 and each dummy equals 1 in half the profiles, so the intercept is calculated as follows.

β^0=4.75−0.5×(−3.00+1.50−1.00)=4.75+1.25=6.00\hat{\beta}_0 = 4.75 - 0.5 \times (-3.00 + 1.50 - 1.00) = 4.75 + 1.25 = 6.00

where β^0\hat{\beta}_0 is the predicted rating of the reference profile, which is a 4-week wait, in hospital, led by a consultant.

2. Check the fit. Fitted ratings match profiles 1, 2, 5 and 6 and miss the others by 0.5, so the residual sum of squares is 1.0 against a total of 25.5, which gives the fit below.

R2=1−1.025.5≈0.961R^2 = 1 - \frac{1.0}{25.5} \approx 0.961

where R2R^2 is the share of rating variation explained by the additive model. Only four degrees of freedom remain, so real studies use more profiles per respondent or pool respondents.

3. Relative importance. The ranges are 3.00, 1.50 and 1.00, so the share for waiting time is calculated as follows.

RIW=3.003.00+1.50+1.00=3.005.50≈0.545RI_W = \frac{3.00}{3.00 + 1.50 + 1.00} = \frac{3.00}{5.50} \approx 0.545

where RIWRI_W is waiting time's share of the total range. Location takes 27.3% and clinic lead 18.2%.

4. Trade-offs in weeks. If value falls linearly between the two waits, the part-worth per week is calculated as follows.

β^week=−3.0012−4=−0.375\hat{\beta}_{week} = \frac{-3.00}{12 - 4} = -0.375

where β^week\hat{\beta}_{week} is the change in rating per extra week. The wait that offsets a local clinic is then as follows.

Δxwait=−1.50−0.375=4.0\Delta x_{wait} = -\frac{1.50}{-0.375} = 4.0

where Δxwait\Delta x_{wait} is the extra weeks this patient would accept to be seen locally. Keeping a consultant lead is worth about 2.7 weeks (1.00 divided by 0.375).

5. Interpretation. For this patient a local nurse-led clinic with a 4-week wait (predicted 6.5) beats the reference hospital consultant clinic with the same wait (6.0), but not if the wait rises to 12 weeks (3.5). These trade-offs rest on treating the scale as interval and on linearity between two observed waits, neither of which the data can test.

Conjoint analysis or discrete choice experiment

Whether choice tasks belong in the family is the main naming dispute. The ISPOR statistical report calls the discrete choice experiment the most common type of conjoint analysis in outcomes research.

Louviere, Flynn and Carson argued in 2010 that discrete choice experiments are not conjoint analysis. In their account traditional conjoint analysis rests on conjoint measurement, a mathematical theory about how numbers behave under factorial manipulation with no error theory, whereas discrete choice experiments rest on random utility theory, which goes back to Thurstone's 1927 work and was extended by McFadden. They argue that ratings do not translate readily into the choice data on which utility theory is based and that many studies claiming to be conjoint analyses are discrete choice experiments, and report that health economists stopped calling choice studies conjoint analyses in the late 1990s.

Hauser and Rao, writing from marketing, describe stated choice models as having all the characteristics of conjoint analysis except the data collection format. The dispute is partly about substance, since only choice data under a random utility model support welfare measures. The family name is used here as the ISPOR reports use it, and random utility models are treated on the choice experiment page.

Outcome weights in health technology assessment and device regulation

Conjoint results reach health decisions mainly as weights for combining outcomes and as evidence on how patients trade benefits against harms. Ryan and Farrar add service uses, such as scoring ways of providing care.

In health technology assessment, Germany's Institute for Quality and Efficiency in Health Care (IQWiG) piloted choice-based weights for its efficiency frontier in 2014, as described on the choice-based conjoint page. IQWiG's General Methods (version 7.0, 2023, section 4.3.3) state that results for several outcomes can be weighted using preference elicitation methods whose applicability is the subject of scientific debate, and that a health economic evaluation under section 35b of Social Code Book V does not include preference surveys conducted by the institute. Surveys submitted in a dossier can be assessed, depending on the commission, provided they contain the outcomes to be considered in the evaluation. Such preference-based outcome weights combine results within a multi-criteria decision analysis and are not the health state utilities behind a QALY.

In device regulation, the US Food and Drug Administration's 2026 guidance on patient preference information cites the ISPOR conjoint analysis checklist and names preference weights and maximum acceptable risk among parameters that can support a benefit-risk assessment.

Where conjoint results mislead

Most errors come from treating outputs as fixed properties of people when they depend on the design and the task. Relative importance depends on the levels chosen, so a 26-week maximum wait would raise waiting time's share in the worked example. Green and Srinivasan report that importance also rises when levels are added between a fixed minimum and maximum; adding two intermediate price levels raised price's importance by seven percentage points in one study.

Ratings-based trade-offs treat the rating scale as cardinal, an assumption Louviere, Flynn and Carson suggest avoiding by using only the order information in ratings; they add that main-effects designs assume untestable additivity and that many conjoint validity tests are hold-out predictions, not comparisons with real behaviour. In a 2011 editorial, Ryan wrote that internal validity tests dominate in health given the lack of a market for health care, called external validity the greatest challenge, and warned that too many attributes may push respondents to rules such as always choosing the cheapest option. Ryan and Farrar dropped inconsistent respondents and non-traders and flagged possible bias. The ten-item ISPOR checklist offers a standard for judging a health conjoint study without endorsing any one method.

Sources

Institutional Perspectives (1)

  • PBAC

    Conjoint Analysis to Value Nonhealth Benefits in a Supplementary Analysis

    The PBAC Guidelines allow direct patient benefits that are not health outcomes, such as a more convenient form of administration, to be valued in a supplementary analysis. Methods to estimate the monetary or other value of the nonhealth benefit may include a conjoint analysis or a discrete choice experiment with a monetary attribute. Where health outcomes do not otherwise differ substantively from the main comparator, the resulting estimate, such as willingness to pay, can enter a supplementary cost-benefit analysis, and any consumer surplus needs a nominated basis for sharing between the sponsor and the taxpayer.

    Guidelines for preparing a submission to the Pharmaceutical Benefits Advisory Committee, version 5.0 (September 2016), Appendix 6 (Including nonhealth outcomes in a supplementary analysis)View source →

Functions & Formulae (4)

R_j = beta_0 + sum_(k=1)^K sum_(l=1)^(L_k) beta_kl * x_jkl + e_j

Maps a respondent's ratings of profiles, each described by levels of several attributes, to a part-worth for each level under an additive model, so that a profile's value is the intercept plus the part-worths of its levels. One level of each attribute is the reference, with a part-worth of zero. Relative importance and trade-offs between attributes follow from the part-worths. The notation follows the Conjoint Analysis article, whose outpatient clinic example is used throughout.

  • Part-worth of a two-level attribute from mean ratings in a balanced orthogonal design

    b_k = Rbar_1 - Rbar_0

    In a balanced orthogonal design with dummy coding, the least-squares part-worth of a two-level attribute equals the mean rating of the profiles showing the coded level minus the mean rating of those showing the reference level. Any design can be fitted by multiple regression on the dummy codes (HE-CF-CJA-001); the difference of means is a shortcut that holds only in a balanced orthogonal design, where every pair of levels of any two attributes appears equally often, as in a full factorial or an orthogonal fraction of it.

  • Predicted rating of a clinic profile under the additive part-worth model

    R_hat = b_0 + b_W * x_W + b_L * x_L + b_N * x_N

    Adds the part-worths of a profile's levels to the intercept, the predicted rating of the reference profile. With three two-level attributes it scores every one of the eight possible clinic designs, including ones not shown to respondents in a fractional design, as long as they combine levels used in the study.

  • Relative importance of a conjoint attribute as its share of the total part-worth range

    RI_1 = r_1 / (r_1 + r_2 + r_3)

    Takes the range of an attribute's part-worths, the difference between its most and least preferred levels over the levels in the study, and divides it by the sum of the ranges of all attributes. Written here for three attributes; with K attributes the denominator has K ranges. The share depends on the levels chosen, so it describes the study's design as much as the respondent.

  • Marginal rate of substitution between two conjoint attributes from part-worths

    dx_b = -b_a / b_b

    Gives the change in a continuous attribute b that offsets a one-unit change in attribute a, so that the profile's value is unchanged: minus the ratio of their part-worths. With waiting time as b it expresses a preference in weeks of waiting; with cost as b it is read as willingness to pay (HE-FM-WTP-001), which is a welfare measure only for choice data analysed under random utility theory.

View all formulae

Library

Publications

8
  • Journal article

    Taking conjoint analysis to task — Ryan M, Vol. 14, No. 4, pp. 401-402 ed., 2011 (Value in Health)

    Editorial on conjoint analysis in health arguing that interaction terms must be specified at the experimental design stage, that tests of internal validity dominate given the lack of a market for health care, and that testing external validity is the greatest challenge facing practitioners.

  • Journal article

    Using conjoint analysis to elicit preferences for health care — Ryan M, Farrar S, Vol. 320, No. 7248, pp. 1530-1533 ed., 2000 (BMJ)

    Paper introducing conjoint analysis for eliciting preferences for health care, which notes that the discrete choice approach has been preferred because choices more closely resemble real decisions and illustrates the method with an orthodontic services application analysed by a random effects ordered probit model.

  • Guidance

    Incorporating Voluntary Patient Preference Information over the Total Product Life Cycle: Guidance for Industry, Food and Drug Administration Staff, and Other Interested Parties — Food and Drug Administration, Issued 30 March 2026, supersedes the guidance issued 24 August 2016 ed., 2026 (Food and Drug Administration)

    Non-binding guidance on patient preference information for medical devices, issued in March 2026 to supersede the 2016 guidance, which states that a discrete choice experiment may be optimal when relative trade-offs among several attributes are needed and lists preference weights, maximum acceptable risk and minimal acceptable benefit among parameters that can support a benefit-risk assessment.

  • Journal article

    Discrete choice experiments are not conjoint analysis — Louviere JJ, Flynn TN, Carson RT, Vol. 3, No. 3, pp. 57-72 ed., 2010 (Journal of Choice Modelling)

    Paper arguing that conjoint analysis rests on conjoint measurement, a theory about numbers with no error theory, whereas discrete choice experiments rest on random utility theory, and that many studies claiming to be conjoint analysis are really discrete choice experiments.

  • Journal article

    Conjoint analysis in marketing: new developments with implications for research and practice — Green PE, Srinivasan V, Vol. 54, No. 4, pp. 3-19 ed., 1990 (Journal of Marketing)

    Review of conjoint analysis in marketing that defines it as any decompositional method estimating the structure of preferences from overall evaluations of a set of alternatives, compares vector, ideal point and part-worth preference models, and reports that an attribute's relative importance rises with its number of levels.

  • Report

    Choice-based Conjoint Analysis: pilot project to identify, weight, and prioritize multiple attributes in the indication "hepatitis C" — Institute for Quality and Efficiency in Health Care (IQWiG), Executive summary of working paper GA10-03, version 1.1 (English translation) ed., 2014 (Institute for Quality and Efficiency in Health Care (IQWiG))

    Executive summary of an IQWiG pilot project that used a discrete choice experiment with patients and healthcare professionals to weight outcomes of antiviral treatment for chronic hepatitis C, finding it feasible for patients to weight patient-relevant outcomes this way while noting that some methodological issues still needed to be solved.

  • Book

    Conjoint analysis, related modeling, and applications — Hauser JR, Rao VR, In: Wind Y, Green PE (eds), Marketing Research and Modeling: Progress and Prospects, pp. 141-168 ed., 2004 (Springer)

    Book chapter on the development of conjoint analysis from conjoint measurement theory, which decomposes an ordinal holistic judgement into interval scales for each attribute, through regression-based estimation to random utility models of stated choice, described as having all the characteristics of conjoint analysis except the data collection format.

  • Journal article

    Conjoint Analysis Applications in Health — A Checklist: A Report of the ISPOR Good Research Practices for Conjoint Analysis Task Force — Bridges, Hauber, Marshall, Lloyd, Prosser, Regier, Johnson & Mauskopf, Vol. 14, No. 4 ed., 2011 (Value in Health)

    The ISPOR good-practice checklist for conjoint analysis and discrete-choice experiments in health — the stated-preference methods used to elicit patient and public preferences over treatment attributes for value assessment and priority-setting.

Frequently Asked Questions (6)

  • What is conjoint analysis?

    Conjoint analysis is a family of stated preference methods estimating how people value treatment or service attributes from ratings, rankings or choices.

    Source: Hauber et al. 2016

  • Where does conjoint analysis come from?

    It originates in work on how a judgement about a combined stimulus can be decomposed into contributions from its separate components, which established the conditions under which such a decomposition is possible. That formal result was taken up in marketing research as a practical way of estimating what buyers value in a product, and later in health to value features of services and treatments. The family therefore rests on a measurement theory rather than on a survey technique, which is what distinguishes it from simply asking people what matters.

    Source: Luce & Tukey 1964

  • What forms does conjoint analysis elicitation take?

    Respondents may rate each described alternative on a scale, rank a set of alternatives in order of preference, or choose one alternative from a set. Rating collects the most information per question and imposes no requirement to trade off, so respondents can score everything favourably. Ranking forces an ordering but not a magnitude. Choice most closely resembles a real decision and yields data suited to established models of choice behaviour, which is why it has become the dominant form in health.

    Source: Green & Srinivasan 1978

  • How are attributes and levels chosen in conjoint analysis?

    Attributes should cover what matters to the decision, be capable of being changed by whoever will act on the results, and be understood consistently by respondents. Levels must span a range that is plausible and wide enough for respondents to notice, since an attribute varied over a narrow range will appear unimportant regardless of how much it matters. The selection is normally developed from qualitative work with the people who will answer, because attributes chosen by analysts routinely omit what respondents actually weigh.

    Source: Ryan, Gerard & Amaya-Amaya 2008

  • What does conjoint analysis produce?

    It produces a weight for each level of each attribute, showing how much that level contributes to the overall attractiveness of an option, from which the relative importance of attributes can be compared. Where one attribute is expressed in money, the weights on the others can be converted into monetary terms. Where one is expressed in health, they can be converted into health terms. The outputs also support prediction of how uptake would change if a service were configured differently.

    Source: Lancsar & Louviere 2008

  • How does conjoint analysis compare with other valuation methods?

    It differs from asking directly what something is worth, since respondents reveal values through choices rather than stating them, which avoids some of the difficulty people have in naming a figure. It differs from methods that value whole health states by valuing the separate features of a service or treatment, which suits questions about how care should be organised. Its results depend on the attributes presented, so it can only value what the analyst thought to include, and this is the constraint that most limits it.

    Source: Bridges et al. 2011

Trust Record

Verified by Dr Darrin Baines

British health economist

Professional identity: darrinbaines.org

Verification date: 28 Oct 2026

Content version: 1.0.1

Canonical Identity

Term code
HE-EE-CBA-010
Wikidata
Q203973

Stable URI · Machine-readable · Resolvable · CC BY 4.0