Evidence map›Paper›PMID 40960789›Full record

Observational studySao Paulo medical journal = Revista paulista de medicina2025

Premenstrual Syndrome-Impact Questionnaire: Cross-cultural adaptation, reliability, and validity of the Turkish version.

Halime Arıkan, Erkan Erol

Registry-linked trialAbstract readObservational StudyValidation Study
In one paragraph

Observational study in Sao Paulo medical journal = Revista paulista de medicina, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05725447 (Cross-cultural Adaptation, Validity and Reliability of the Turkish Version of the Premenstrual Syndrome Impact Questionnaire), which is not on this map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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.

NCT05725447 completednot on this map

Cross-cultural Adaptation, Validity and Reliability of the Turkish Version of the Premenstrual Syndrome Impact Questionnaire (PMS-IQ)

TypeobservationalSponsorGazi UniversityRan2022 to 2022Enrolled200ConditionsPremenstrual SyndromeArmsValidity and reliability study
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

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5 · Who and what money

Authors and funding

2 authors.

Halime ArıkanPhysiotherapist, Assistant Professor, Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Tokat Gaziosmanpaşa University, Tokat, Türkiye.ORCID 0000-0003-2381-9978
Erkan ErolPhysiotherapist, Assistant Professor, Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Tokat Gaziosmanpaşa University, Tokat, Türkiye.ORCID 0000-0002-0087-1821

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundShort and practical questionnaires and tests that assess premenstrual symptoms and premenstrual syndrome (PMS) are required.

objectivesThis study aimed to investigate the cross-cultural adaptation, validity, and reliability of the Premenstrual Syndrome Impact Questionnaire (PMS-IQ) in Turkish women with PMS. DESIGN AND

settingThe reliability and validity of the questionnaire were evaluated in Tokat, Türkiye.

methodsA convenience sample of 146 individuals diagnosed with PMS was used to assess the reliability and validity of the Turkish version of the PMS-IQ. Test-retest analyses were performed in a subset of 96 individuals one week after the initial assessment. Construct validity was evaluated through convergent validity analysis using the Premenstrual Syndrome Scale (PMSS) and the Premenstrual Symptoms Impact Survey (PMSIS), and divergent validity analysis with the Big Five Inventory-10 (BFI-10).

resultsCronbach's α values for the total score and subscales ranged from 0.861 to 0.917, whereas the test-retest reliability values ranged from 0.755 to 0.847. Factor analysis indicated that the scale had a three-factor structure. The total PMS-IQ score was significantly correlated with both the PMSS (r = 0.718) and PMSIS (r = 0.774), but showed no significant correlation with the BFI-10 (r = 0.113). No floor or ceiling effects were observed for the total or subscale scores of the PMS-IQ.

conclusionsThe Turkish version of the PMS-IQ demonstrated reliability and validity for evaluating individuals with PMS. CLINICAL

trial registrationThis study is registered at ClinicalTrials.gov (identifier: NCT05725447).

Indexed as

Premenstrual SyndromeAdolescentAdultCross-Cultural ComparisonFemaleHumansMiddle AgedPsychometricsReproducibility of ResultsSurveys and QuestionnairesTranslationsTurkeyYoung Adult

Identifiers

PMID40960789
PMCPMC12440256

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Registered trials

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