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Turkish Version of the Pictorial Pain Interference Questionnaire

Assessment of the Functional Impact of Chronic Pain: Psychometric Properties of the Turkish Version of the Pictorial Pain Interference Questionnaire

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07761208
Enrollment
100
Registered
2026-08-12
Start date
2026-08-20
Completion date
2027-02-22
Last updated
2026-08-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain, Pain Management

Keywords

Chronic Pain, Pain Interference, Pictorial Pain Interference Questionnaire, Psychometric Properties, Turkish Version

Brief summary

This study aims to culturally adapt the Pictorial Pain Interference Questionnaire into Turkish and evaluate its psychometric properties in individuals with chronic pain. The study will assess the validity and reliability of the Turkish version for evaluating the functional impact of chronic pain on daily life activities. Reliability will be examined through internal consistency and test-retest reliability, while validity will be assessed by examining the relationships between the questionnaire and established pain-related assessment tools. The study will determine whether the Turkish version provides a valid, reliable, and practical instrument for assessing functional interference associated with chronic pain in Turkish-speaking individuals.

Interventions

OTHERNo Interventions

This is an observational psychometric validation study. Participants are not assigned to receive any therapeutic intervention; they complete the questionnaires and assessments specified in the study protocol.

Sponsors

Istinye University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Having chronic pain lasting for at least 3 months. * Willing to participate in the study and providing informed consent. * Having sufficient cognitive ability to understand the questions.

Exclusion criteria

* Severe cognitive impairment (e.g., dementia) or conditions that interfere with communication. * Inability to cooperate due to a psychiatric disorder. * Neurological or serious systemic diseases that may affect the assessment. * Incomplete or incorrectly completed questionnaires. * Refusal to participate or withdrawal from the study.

Design outcomes

Primary

MeasureTime frameDescription
Internal Consistency of the Turkish Pictorial Pain Interference QuestionnaireAt the first assessment (Baseline)Internal consistency will be assessed using Cronbach's alpha coefficient.
Test-Retest Reliability of the Turkish Pictorial Pain Interference QuestionnaireBaseline and 7 daysTest-retest reliability will be assessed using the Intraclass Correlation Coefficient (ICC) based on assessments performed 7 days apart.
Construct Validity of the Turkish Pictorial Pain Interference QuestionnaireBaselineConstruct validity will be evaluated by examining the correlations between the questionnaire scores and scores from the Brief Pain Inventory.

Secondary

MeasureTime frameDescription
Discriminant Validity of the Turkish Pictorial Pain Interference QuestionnaireBaselineDiscriminant validity will be assessed by examining correlations with concepts expected to have weak associations with pain, including positive affect.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 13, 2026