CSEG3060 · Research Methodology in Computer Science

Ethical Considerations in Research

Informed consent · confidentiality · fabrication and falsification · authorship norms · conflict of interest

Research rests on trust. Every rule in this lecture exists because trust can be broken at a specific point.

Unit III · Lecture 7 of 8 · 60 minutes · CO3

Dr. Mohsin Furkh Dar · School of Computer Science, UPES

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Learning objectives · CO3

By the end of this session, you can…

01

Define and apply informed consent in human-subjects research

02

Explain the mechanisms that preserve confidentiality and protect data

03

Distinguish fabrication, falsification and legitimate data transformation

04

Identify criteria for legitimate authorship and the cost of honorary or ghost authorship

05

Recognise, disclose and manage conflicts of interest

06

Connect each principle to concrete computer science scenarios

CSEG3060 · Unit III · Lecture 7 — Ethical Considerations in Research2

Orientation

Five domains — and who each one protects

DomainCore principlePrimary risk if violatedWho is protected
Informed consentVoluntary, informed, capacitated agreementCoercion, exploitationParticipants
ConfidentialityPrivacy protection and controlled disclosurePrivacy breach, identity exposureData subjects
Fabrication / falsificationHonest data collection and reportingLoss of scientific validityReaders and the record
Authorship normsCredit for substantial intellectual contributionMisattribution of creditCollaborators
Conflict of interestTransparent disclosure of competing interestsCompromised objectivityThe public and peer review

Why this binds computing

CS research now involves human participants (HCI, user studies, AI fairness), large-scale personal datasets, and multi-institution collaborations — each activating a different ethical regime.

Regulatory anchors

Belmont principles · Declaration of Helsinki · ICMR National Ethical Guidelines (2017) · DPDPA 2023 and GDPR · ICMJE and COPE · ORI misconduct definitions

CSEG3060 · Unit III · Lecture 7 — Ethical Considerations in Research3

Pillar 1 · part 1

Five components of valid consent

Consent is a process, not a signature: voluntary agreement after being fully informed of purpose, procedures, risks, benefits, alternatives and data handling. Rooted in Belmont's respect for persons; reaffirmed in Article 6 of the Declaration of Helsinki.
Disclosure
→
Understanding
→
Voluntariness
→
Capacity
→
Documentation

Disclosure

Purpose, duration, procedures, foreseeable risks, expected benefits, compensation.

Understanding

Language the participant comprehends — free of jargon and undue influence.

Voluntariness

Free from coercion or penalty for refusal — a live concern when you recruit classmates or juniors.

Capacity

Legal and cognitive capacity; surrogate or parental consent for minors and incapacitated individuals.

Documentation

Normally a signed form; click-through or recorded verbal consent is acceptable in some digital contexts.

A consent form written at postgraduate reading level fails the understanding criterion no matter how complete its disclosure.

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Pillar 1 · part 2

The hard cases in computing

Crowdsourcing — MTurk, Prolific

Consent must be obtained before task exposure. IP addresses and metadata may themselves constitute identifiable information even when no name is collected.

Secondary use of existing datasets

Reuse beyond the original consent's scope may violate the agreement under which data were collected — however public the dataset now appears.

Industry A/B testing

Many firms experiment on users without explicit consent, raising unresolved concerns about autonomy and transparency. A practice being routine does not settle whether it is ethical.

Worked example

A usability study of a new authentication mechanism, 100 participants. Each must be told:

  • that they may withdraw at any time
  • that their keystroke dynamics will be collected
  • how the data will be stored and destroyed
  • whom to contact with grievances
Failure to disclose the keystroke logging is a violation even if the protocol received institutional approval. Committee approval does not substitute for participant disclosure.
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Pillar 2 · part 1

The obligation, the distinction, the regulators

The obligation to protect participants' private information and prevent unauthorised access, use or disclosure.

Identified

Identifiers present. Directly attributable to a person.

Pseudonymised

Identifiers replaced by keys held separately — still re-identifiable, so not anonymisation under GDPR.

Anonymised

Link destroyed. Cannot be traced back to an individual.

Four operational practices

  1. Minimisation — collect only what the question requires
  2. Anonymisation or pseudonymisation — remove or replace identifiers
  3. Secure storage — encryption, access controls, audit logs
  4. Controlled access — authorised personnel under binding agreements

Regulatory frameworks

India — DPDPA 2023 · EU — GDPR · US — HIPAA for medical data

Minimisation is the strongest safeguard: data never collected cannot be breached, subpoenaed, re-identified or leaked.

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Pillar 2 · part 2

Technical mechanisms — and their costs

Encryption

TLS 1.3 in transit, AES-256 at rest. The baseline expectation, not an advanced measure.

Cost: negligible.

Differential privacy

Calibrated noise so the presence or absence of any individual cannot be inferred — bounding re-identification risk mathematically rather than by assertion.

Cost: accuracy, against the privacy budget.

Federated learning

Training across devices or institutions without transferring raw data — the architecture used where data cannot lawfully be pooled.

Cost: efficiency; leakage via model updates.

Secure multi-party computation

Joint computation over inputs that no party reveals to the others.

Cost: computationally expensive.

Most relevant in health informatics, social-network analysis and behavioural analytics — the subfields where confidentiality obligations are strictest and research questions most demanding.

None is a complete solution. Technical safeguards reduce risk; they do not replace consent.
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Pillar 3 · part 1

Fabrication, falsification — and legitimate transformation

Fabrication

Making up data, results or records and reporting them as real.

Falsification

Manipulating materials, equipment or processes, or changing, omitting or selectively reporting data so the research is not accurately represented.

Plagiarism

Appropriating another's ideas, processes, results or words without credit — Lectures 4 and 5.

PracticeEthical status
Removing outliers with documented statistical justificationGenerally acceptable
Applying anonymisation or aggregationAcceptable, often required
Cherry-picking supportive results while omitting null findingsUnethical — selective reporting
Generating synthetic data to fill missing records without disclosureUnethical — fabrication
Re-running an experiment until the result is significantUnethical — manipulation
Image manipulation that alters figure contentUnethical — falsification
Two discriminating variables: disclosure and documentation. Synthetic data disclosed as synthetic is a method; the same data presented as observed is fabrication. Note that the ORI definition includes omitting.
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Pillar 3 · part 2

Where falsification enters a CS experiment

Dataset selection
→
Hyperparameter tuning
→
Metric selection
→
Run reporting

Benchmark falsification

Cherry-picking benchmarks, omitting unfavourable datasets and tuning hyperparameters on the test set are all falsification — notwithstanding that each step looks like ordinary engineering iteration.

Test-set contamination

Once the test set has informed a design decision, the reported number is a training-set estimate presented as a generalisation estimate — a misrepresentation of what the experiment measured.

Image manipulation

Figures in computational biology and imaging can be altered in general-purpose editors — which is why journals now require raw image data alongside submitted figures.

The reproducibility crisis

Many published ML results cannot be replicated, substantially because of undisclosed preprocessing and selective reporting rather than outright invention.

Documented cases

Jan Hendrik Schön (2002) — fabricated data across semiconductor studies at Bell Labs.
Hwang Woo-suk (2004–05) — fabricated stem-cell data; retraction and criminal conviction.
Contemporary cases are catalogued by Retraction Watch.

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Pillar 4 · part 1

ICMJE's four criteria — all four, not any one

The four ICMJE criteria — conjunctive

  1. Substantial contribution to conception, design, data acquisition, analysis or interpretation
  2. Drafting or critical revision for important intellectual content
  3. Final approval of the version to be published
  4. Accountability for all aspects of the work

Contributors meeting fewer than four should be acknowledged, not listed.

Criterion 4 is the one students overlook: accepting authorship means accepting answerability for the whole paper, including parts you did not produce — which is why a gift author is exposed, not merely flattered.

MisconductDescription
Gift authorshipListing senior colleagues without their meaningful contribution
Guest authorshipAdding a well-known researcher to enhance credibility
Ghost authorshipOmitting a contributor who made substantive contributions
Coercive authorshipSenior authors pressuring juniors to include unrelated contributors
Mutual-benefit authorshipReciprocal name-swapping across papers without genuine contribution

COPE and ICMJE are the standards journals apply when an authorship dispute is escalated.

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Pillar 4 · part 2

CRediT, mega-author papers and the advisor–student asymmetry

ICMJE criteria were designed around individually authored manuscripts. CS produces collaboratively built software, datasets and infrastructure whose contributors do not map cleanly onto drafting and revision.

CRediT — 14 roles: conceptualisation · methodology · software · validation · formal analysis · investigation · data curation · writing – original draft · writing – review and editing · visualisation · supervision · project administration · funding acquisition · resources

Mega-author papers

Submissions at venues such as NeurIPS may carry 30 or more authors, at which point a byline conveys almost no information and per-role contribution statements become the only meaningful transparency.

Advisor–student dynamics

A student who is the primary contributor should be listed as first author. The power asymmetry means the student rarely raises it — so the remedy is a documented authorship agreement before work begins, not a negotiation after submission.

Software, data curation and validation are the roles this cohort most often fills uncredited. Naming them explicitly is how the contribution becomes visible.

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Pillar 5 · practical application

Types, disclosure duty and the management ladder

A COI exists when personal, financial, professional or institutional interests could compromise — or appear to compromise — the objectivity, integrity or independence of the research. Appearance is sufficient.

Financial

Stock, consulting fees, royalties, honoraria from parties who benefit from the outcome.
Evaluating a self-driving system funded by its manufacturer.

Personal

Close relationships with individuals or organisations.
Benchmarking against a competing library you maintain.

Institutional

Pressure from a funder whose product is under evaluation.

Intellectual

Strongly held theoretical commitments that bias interpretation.

Political / ideological

Acutely relevant in AI ethics, algorithmic fairness and policy research.

Disclosure requirements

IEEE, ACM, NeurIPS and ICML all require declaration of funding sources, employment, equity interests, advisory memberships and any other relevant relationship within roughly the past three years.

Management ladder

Disclose → blind → independent oversight → recompose the team → recuse. Disclosure is the floor.

Failure to disclose is itself a violation, regardless of whether the research was actually biased.
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Case studies

Four scenarios, and who catches them

ScenarioDomainLesson
A fairness paper reports a 2% parity gap computed on a favourable dataset subset; retractedFalsificationSelective reporting and benchmark manipulation are falsification
A platform runs a large-scale A/B test manipulating emotional valence of feeds; published without consentInformed consentScale does not suspend the consent obligation
A company's medical writer drafts a manuscript; only academic authors listed; writer later untraceableAuthorship (ghost)Ghost authorship destroys accountability; breaches ICMJE
A researcher praises an AI hiring tool; stock options in the vendor emerge laterConflict of interestNon-disclosure undermines the credibility of the finding

Who catches these

  • IRB / Ethics Committees — human-subjects protocols
  • IECs under ICMR guidelines in India
  • Research Integrity Offices — misconduct allegations
  • Funding agencies — DST, SERB, UGC: ethics training and certification

Consequences

Retraction · funding blacklist · termination · degree revocation · civil or criminal liability where data-protection law is breached. Confirmed cases are documented publicly by Retraction Watch.

Scenarios are illustrative composites for teaching. The interdependence point: case 2 implicates consent and confidentiality; case 1 implicates falsification and authorship accountability.

CSEG3060 · Unit III · Lecture 7 — Ethical Considerations in Research13

Consolidation

Five takeaways, and four scenarios to decide

Five takeaways

  • Consent — voluntary, informed, capacitated, documented; approval ≠ disclosure
  • Confidentiality — technical and procedural; distinguish anonymity from pseudonymity
  • Fabrication/falsification — honest reporting is non-negotiable; omission counts
  • Authorship — credit tracks substantial contribution; use CRediT
  • COI — disclose all relevant interests; manage or recuse

Scenario 1

A PhD student wants to scrape user reviews from a public website for sentiment analysis. Identify the ethical concerns and propose safeguards.

Scenario 2

Three students collaborate; one writes the paper, the other two did coding and analysis, all three are listed. Evaluate against ICMJE.

Scenario 3

You are reviewing a paper and notice the lead author co-founded the startup whose product is evaluated. What do you do?

Scenario 4

A dataset contains personal data and its terms prohibit re-identification. Discuss the ethical and legal implications.

Failure in one domain cascades into others: falsification typically also misleads co-authors, converting a data offence into an authorship and trust offence.
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Exam preparation

Distinctions, bodies and answer technique

What is tested

  • Definitions: fabrication · falsification · informed consent · ICMJE criteria · COI
  • Distinctions: confidentiality vs anonymity (and pseudonymisation) · fabrication vs falsification · gift vs ghost authorship · legitimate transformation vs selective reporting
  • Bodies and instruments: IRB/EC · ICMR (2017) · ICMJE · COPE · ORI · Retraction Watch · GDPR · DPDPA (2023) · HIPAA

Answer technique

Definition → principle → CS example → consequence. Always ground the example in computing — HCI, datasets, benchmarking, AI fairness — rather than medical research. State the institutional and legal ramifications.

Expect applied items

Given a scenario: identify the violated domain, name the governing standard, prescribe the remedy.

Further reading: Belmont Report (1979) · Declaration of Helsinki (rev. 2013) · ICMR National Ethical Guidelines (2017) · DPDPA (2023) · GDPR · ICMJE Recommendations · COPE Guidelines · ORI Introduction to RCR · Retraction Watch.

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