
Clinician guide
How to Calculate Interval-by-Interval IOA
Divide occurrence or nonoccurrence interval agreements by matched intervals, report prevalence, and recognize when many empty intervals make agreement look strong.
Clinical guides, tools, and evidence-informed resources for thoughtful, high-quality ABA care.

Clinician guide
Divide occurrence or nonoccurrence interval agreements by matched intervals, report prevalence, and recognize when many empty intervals make agreement look strong.

Clinician guide
Match the same eligible trials, divide agreements by trials compared, and keep invalid, missing, prompted, or differently defined ABA trials visible.

Clinician guide
Divide intervals with identical observer counts by intervals compared, preserve interval records, and interpret the method's sensitivity to any count difference.

Clinician guide
Calculate smaller divided by larger count in each matched interval, average interval agreements, preserve raw counts, and define how zero-zero intervals are handled.

Clinician guide
Calculate smaller total count divided by larger total count, verify matched exposure, preserve observer counts, and recognize temporal disagreement hidden by totals.

Clinician guide
Document definitions, units, exposure, conversion assumptions, overlap, calibration, and discontinuities when ABA data move between measurement systems.

Clinician guide
Encode missing, invalid, late, corrected, not-due, zero-opportunity, and true-zero ABA data without connecting unknown periods or converting gaps to zero.

Clinician guide
Measure eligible opportunities per time, separate response performance from opportunity availability, and interpret ABA count changes with environment data.

Clinician guide
Distinguish a mean of session percentages from a pooled opportunity percentage, weight by the correct exposure, and keep incompatible ABA conditions separate.

Clinician guide
Inspect raw durations, median, mean, range, percentiles, exposure, open-ended events, and context when a few long observations skew ABA data.

Clinician guide
Define a response window, preserve no-response trials apart from observed latency, and summarize ABA timing data without treating the window maximum as a response.

Clinician guide
Calculate event rate per time and response rate per eligible opportunity, interpret opportunity density, and choose the unit that matches the clinical question.