Evidence map›Paper›PMID 41264134›Full record

Trial reportJournal of patient-reported outcomes2025

Psychometric evaluation of a pediatric functional constipation symptom diary using randomized phase 3 clinical trial data.

Julia Vishnevetsky, Masakazu Ando, Yanqing Xu, Xiaolan Ye, Jessica L Abel

Erratum issued Registry-linked trialAbstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in Journal of patient-reported outcomes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT04026113 (A Phase 3, Multicenter, Randomized, Double-blind, Parallel-group, Safety and Efficacy Study of Linaclotide in Pediatric Participants, Ages 6 to 17 Years, With Irritable Bowel Syndrome With Constipation), which is not on this 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.

NCT04026113 phase3completednot on this map

A Phase 3, Multicenter, Randomized, Double-blind, Parallel-group, Safety and Efficacy Study of Linaclotide in Pediatric Participants, Ages 6 to 17 Years, With Irritable Bowel Syndrome With Constipation (IBS-C) and of Linaclotide Versus Placebo in Pediatric Participants With Functional Constipation (FC)

TypeinterventionalSponsorAbbVieRan2019 to 2024Enrolled438ConditionsFunctional Constipation, Irritable Bowel Syndrome With ConstipationArmsLinaclotide, Placebo
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

5 · Who and what money

Authors and funding

5 authors.

Julia VishnevetskyAbbVie, Inc., Florham Park, NJ, USA.ORCID http://orcid.org/0009-0007-2807-1715
Masakazu AndoIronwood Pharmaceuticals, Boston, MA, USA.
Yanqing XuAbbVie, Inc., North Chicago, IL, USA.
Xiaolan YeAbbVie, Inc., North Chicago, IL, USA.
Jessica L AbelAbbVie, Inc., Florham Park, NJ, USA. jessica.abel@abbvie.com.

Funding

AbbVie AbbVieIronwood Pharmaceuticals, Incorporated Ironwood Pharmaceuticals, Incorporated
6 · The paper itself

Abstract

backgroundPatient-reported outcomes (PROs) are required to assess the efficacy of treatments for functional constipation (FC), which is one of the most common functional gastrointestinal disorders in children. A novel PRO, the Pediatric Functional Constipation Symptom Diary (PFCSD), was developed to assess 7 core symptoms of FC (stool frequency, stool consistency, incomplete evacuation, straining, abdominal pain, abdominal bloating, and fecal incontinence) in pediatric FC patients. Here, we describe the psychometric analyses of the PFCSD using data from a phase 3 clinical trial of linaclotide (LIN-MD-64; NCT04026113) in children with FC. METHODOLOGY: This psychometric evaluation assessed the measurement properties (reliability, validity, responsiveness) and meaningful within-patient change thresholds for symptom scores derived from the PFCSD. Since spontaneous bowel movement (SBM) frequency and stool consistency (measured using the pediatric Bristol Stool Form Scale in the PFCSD) were key endpoints for the phase 3 clinical trial of linaclotide, scores from these 2 items were the primary focus of these psychometric analyses. Daily and weekly responses on the PFCSD were assessed across a 14-week period from 328 pediatric patients aged 6 to 17 years who met the modified Rome III criteria for child/adolescent FC.

resultsTest-retest reliability, construct validity, and responsiveness of SBM frequency and stool consistency scores on the PFCSD were supported by this psychometric evaluation. Using intraclass correlation coefficients (ICCs), PFCSD scores on items measuring SBM frequency (ICC = 0.91) and stool consistency (ICC = 0.56) were consistent across repeated administrations. Convergent and discriminant correlations underscored the validity of SBM frequency and stool consistency scores on the PFCSD. The meaningful change threshold for weekly SBM frequency was identified as a change from baseline of ≥ 2 SBMs. For stool consistency, the meaningful change threshold ranged between + 0.8 to + 1.7 on the pediatric Bristol Stool Form Scale.

conclusionsThe PFCSD is a novel, fit-for-purpose PRO measure evaluating key symptoms experienced by patients with FC aged 6 to 17 years. These analyses support the reliability, validity, and responsiveness of SBM frequency rate and stool consistency scores on the PFCSD in this target population and provide further guidance for interpreting meaningful changes in these scores at the individual level.

Indexed as

ConstipationDiaries as TopicPatient Reported Outcome MeasuresPeptidesAdolescentChildFemaleHumansMalePsychometricsReproducibility of ResultslinaclotidePeptidesPatient-reported outcomesPediatric functional constipationPsychometric evaluation

Identifiers

PMID41264134
PMCPMC12635004

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Registered trials

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.