Evidence map›Paper›PMID 42144889›Full record

ArticleStatistics in medicine2026

Interrupted Time Series Methods for Nonrandom Sampling Study Designs With Known Sampling Weights.

Thuy V Lu, Joshua D Grill, Daniel L Gillen, Maricela Cruz

Abstract read
In one paragraph

Article in Statistics in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Thuy V LuDepartment of Statistics, University of California, Irvine, California, USA.
Joshua D GrillInstitute for Memory Impairments and Neurological Disorders, University of California, Irvine, California, USA.
Daniel L GillenDepartment of Statistics, University of California, Irvine, California, USA.
Maricela CruzDepartment of Biostatistics, University of Washington, Seattle, Washington, USA.ORCID https://orcid.org/0000-0003-1644-9913

Funding

UC Irvine Alzheimer's Disease Research Center Induced Pluripotent Stem Cell CoreP50AG016573 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI LAFERLA, FRANK M · 2000 to 2019
$37.0M
Training in the Neurobiology of Aging and Alzheimers DiseaseT32AG000096 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI VIVEK SWARUP, Craig E Stark · 1985 to 2026
$9.6M
Recruiting and retaining participants from disadvantaged neighborhoods in registriesR01AG077628 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI Daniel L Gillen, Joshua Grill · 2022 to 2026
$3.7M
Statistical Methods for Alzheimer's ResearchRF1AG075107 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI GILLEN, DANIEL L, NAN, BIN · 2022 to 2025
$1.7M
NIA NIH HHS P50 AG016573NIA NIH HHS R01 AG077628NIA NIH HHS R01AG077628NIA NIH HHS RF1 AG075107NIA NIH HHS T32 AG000096NIA NIH HHS T32AG00096
6 · The paper itself

Abstract

Including participants from diverse neighborhoods in research may improve generalizability of study results to broader populations. The University of California Irvine Consent-to-Contact (C2C) Registry recently initiated a novel Recruitment Strategy Study (named the C2C-RSS) to assess the effectiveness of interventions (Facebook versus traditionally mailed postcard advertisements) that aimed at recruiting individuals from more disadvantaged neighborhoods, as defined by high Area Deprivation Index (ADI) in Orange County, California. The C2C-RSS utilized a nonrandom sampling design to ensure uniform inclusion across ADI deciles. The primary objective of the C2C-RSS is to estimate a marginal intervention effect across all ADI deciles on recruitment to the C2C Registry. A key secondary objective is to assess effect modification by ADI strata. To adjust for sampling bias in the C2C-RSS design, we extend the Robust-Multiple Interrupted Time Series model to incorporate known sampling weights. We additionally propose two variance estimators. The first quantifies uncertainty of the unknown change point associated with the intervention in all mean function parameters. The second additionally accounts for mis-specification of the mean model. We demonstrate the performance of our methods through empirical simulation studies. Further, we use our proposed methods to assess the design of the C2C-RSS, illustrating comparable power for the primary endpoint and increased power for the secondary endpoint relative to a simple random sampling design.

Indexed as

Interrupted Time Series AnalysisCaliforniaComputer SimulationHumansModels, StatisticalPatient SelectionRegistriesResearch DesignSampling StudiesSelection Biaschange point variabilityinterrupted time seriesintervention assessmentknown sampling weightsmultiple unitsweights

Identifiers

PMID42144889
PMCPMC13537023

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.