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Patient–provider communication for chronically ill patients: gender- and age-specific preferences of patients

Patient–provider communication for chronically ill patients: gender- and age-specific preferences of patients - PaBeKo

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00000762
Enrollment
900
Registered
2011-07-29
Start date
2008-03-09
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Chronic back pain Chronic ischemic heart disease M47.1 M47.2 M47.8 M47.9 M48.1 M48.2 M48.8 M48.9 M51.0 M51.1 M51.2 M51.3 M51.4 M51.8 M51.9 M53.8 M53.9 M54.1 M54.3 M54.4 M54.5 M54.8 M54.9 F45.4 I25

Interventions

Group 1: The PaBeKo-project consisted of four partial studies, two pre-studies and two main studies. We included one group of participants (chronically ill patientes = chronic back pain or chronic isc

Sponsors

Uniklinikum Freiburg Abteilung Qualitätsmanagement und Sozialmedizin (AQMS)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Diagnosis "Chronic back pain" or "Chronic ischemic heart disease"

Exclusion criteria

Exclusion criteria: Language impairment; cognitive and/or physical impairment (patient is not able to fill out questionnaire)

Design outcomes

Primary

MeasureTime frame
The primary aim of this research project is the development and the methodological examination of an instrument that measures preferences of chronically ill patients in relation to patient-provider communication (Questionnaire for patients’ communication preferences [the KOPRA questionnaire]). The questionnaire should be in accordance with the test theoretical requirement of Rasch’s Model. Simulatenously it is anticipated to develop of a comparable instrument for providers (Questionnaire for providers’ atttitudes towards communication [the KOMBEIN questionnaire]) and a questionnaire for testing communicative behavior of providers (KOVA questionnaire).

Secondary

MeasureTime frame
During further course of this study quantitative data collection will be exercised. It will based on the newly developed measuring instruments. Data collection is supposed to identify possible influencing factors on patients’ peferences. This is done by analysing different preference of a) female and male patients. b) patients in different age groups. c) patients with different types of diagnosis. d) stationary/ambulant patients

Countries

Germany

Contacts

Public ContactLukas Gramm

Universitätsklinikum Freiburg Abteilung für Qualitätsmanagement und Sozialmedizin (AQMS)

lukas.gramm@uniklinik-freiburg.de0761-27074280

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026