Use when designing or auditing the studies behind an ACM CHI paper — matching evidence shape to contribution type, powering quantitative experiments, making qualitative work rigorous and auditable, reporting participants and ethics properly, and avoiding the ADR-Data and ADR-Method screening grounds.
Scanned 9/5/2026
Install to Claude Code
npx -y skills add brycewang-stanford/Awesome-Journal-Skills --skill chi-experiments --agent claude-codeInstalls into .claude/skills of the current project.
Are you the author of Chi Experiments?
Add the live security badge to your README — it updates automatically with every re-scan.
[](https://www.skillsdirectory.com/skills/brycewang-stanford-chi-experiments)More formats (shields.io, HTML) on the badges page.
---
name: chi-experiments
description: Use when designing or auditing the studies behind an ACM CHI paper — matching evidence shape to contribution type, powering quantitative experiments, making qualitative work rigorous and auditable, reporting participants and ethics properly, and avoiding the ADR-Data and ADR-Method screening grounds.
---
# CHI Experiments and Studies
"Experiments" at CHI means human evidence: controlled lab studies, field deployments,
interview and diary studies, surveys, log analyses, and mixtures of these. Two of the
four assisted desk-reject rubric grounds CHI now screens with — **ADR-Data** (grossly
insufficient data for the claims) and **ADR-Method** (grossly insufficient
methodological detail or transparency) — are study-design judgments made *before full
review*. Evidence design is therefore survival, not polish.
## Match the evidence to the claim, not to habit
| Claim shape | Evidence that convinces CHI reviewers | Chronic mismatch seen in reviews |
|---|---|---|
| "Technique X outperforms Y" | Controlled comparison, counterbalanced, powered, effect sizes | Underpowered n=12 with p-values only |
| "Users experience/need Z" | Interviews or diary study to saturation, systematic analysis | Cherry-picked quotes, no analysis method stated |
| "System S is usable/useful in practice" | Field deployment with real tasks over time | One-hour lab walkthrough of a demo |
| "Population P interacts differently" | Sampling strategy that can reach P, comparative design | Convenience sample of students standing in for P |
| "Design guideline G holds" | Multiple probes/instantiations, triangulated methods | Single prototype, single context, universal claim |
| "Measure M captures construct C" | Validation study: reliability, convergent validity | New questionnaire used, never validated |
Mixed methods are a CHI signature: a quantitative result explains *that*, the paired
qualitative strand explains *why*. If you run both, integrate them in the analysis —
a qualitative section bolted after the ANOVA reads as decoration.
## Quantitative discipline
- **Power before running.** Decide the smallest effect worth detecting, then size the
study; report the analysis. Post-hoc power excuses convince nobody.
```python
# a priori sample size for a within-subjects comparison (paired t-test)
from statsmodels.stats.power import TTestPower
n = TTestPower().solve_power(effect_size=0.5, alpha=0.05, power=0.8,
alternative="two-sided")
print(round(n)) # ≈ 34 participants for d=0.5 — n=12 detects only d≈0.88
```
- Report **effect sizes with confidence intervals** alongside test statistics; CHI's
methods community has campaigned against naked p-values for a decade.
- State the analysis plan's provenance: preregistered, planned-but-unregistered, or
exploratory. Label exploratory findings as such instead of promoting them.
- Check assumptions (normality, sphericity) and name the corrections used; Likert
and time data routinely need non-parametric or transformed treatment.
- Counterbalance and report order effects for within-subjects interaction studies.
## Qualitative discipline
Qualitative work at CHI is judged on rigor, not sample size. What reviewers audit:
- The **named analysis method** actually followed — reflexive thematic analysis,
grounded-theory procedures, interaction analysis — with its own reporting
conventions honored (e.g., do not report inter-rater reliability for reflexive TA
while claiming a codebook emerged from consensus; pick a coherent paradigm).
- **Recruitment, who the participants are, and what they were paid**, in a table.
- Enough **quote evidence per theme** to show the theme is in the data, attributed
with participant IDs (P1–Pn), balanced across participants.
- **Researcher positionality** where the topic makes the researcher's standpoint
analytically relevant (common in accessibility, health, and marginalized-community
work) — a norm in parts of CHI, not a universal requirement.
## Participants and ethics are results-page material
CHI reviewers read the participants section as evidence, and screening cites it:
1. Recruitment channel and criteria; compensation and its local adequacy.
2. Ethics approval (IRB or equivalent) named, or the honest statement of why the
jurisdiction requires none — plus consent procedure for data, recordings, and
any footage reused in the video figure (`chi-supplementary`).
3. Demographics reported to the level the claims need: an accessibility claim needs
disability descriptions; a cross-cultural claim needs more than "US and EU".
4. Risks and mitigations for sensitive topics; deception disclosed and debriefed.
5. Data handling: anonymization, storage, deletion timeline.
## Deployment and AI-system studies
For field deployments, report duration, retention, and usage telemetry honestly —
attrition is data. For AI-infused interfaces, evaluate both the model and the human
experience: state model version, prompts/configurations, and failure behavior during
the study window, because "users trusted the system" is uninterpretable without
knowing how often the system was wrong. Pin model versions; a study run on a moving
API is unreplicable by construction (`chi-reproducibility`).
## Pre-submission evidence audit
Walk each headline claim backwards: which figure/table/theme supports it, from which
data, collected from whom, analyzed how? Any claim that dead-ends is either cut,
scoped down ("in our lab task, for our participants..."), or flagged as future work.
This single pass defuses most ADR-Data exposure.
## Output format
```text
[Contribution type] <from chi-topic-selection>
[Evidence inventory] <study 1: design, n, analysis> · <study 2: ...>
[Claim-evidence dead ends] <claims without support, or none>
[Quant status] power: <basis> / effect sizes+CIs: yes/no / plan provenance: prereg|planned|exploratory
[Qual status] method named+followed: yes/no / quotes balanced: yes/no
[Ethics] approval: <body or n/a+reason> / compensation: <amount> / consent for footage: yes/no
[ADR exposure] Data: low/med/high · Method: low/med/high — <weakest point>
```
Is this your skill, or is something wrong with this listing? Request removal or report an issue. Author removals are honored within 72 hours.
No comments yet. Be the first to comment!