Alternative title
Latent profile analysis of co-care experiences
Creator/Principal investigator(s)
Carolina Wannheden
- Karolinska Institutet, Department of Learning, Informatics, Management and Ethics (LIME)
Marta Roczniewska
- Karolinska Institutet, Department of Learning, Informatics, Management and Ethics (LIME)
Henna Hasson
- Karolinska Institutet, Department of Learning, Informatics, Management and Ethics (LIME)
Klas Karlgren
- Karolinska Institutet, Department of Learning, Informatics, Management and Ethics (LIME)
Ulrica von Thiele Schwarz
- Karolinska Institutet, Department of Learning, Informatics, Management and Ethics (LIME)
Description
This data description contains code (written in the R programming language), as well as processed data and results presented in a research article (see references). No raw data are provided and the data that are made available cannot be linked to study participants. The sample consists of 180 of 308 eligible participants (adult primary care patients in Sweden, living with chronic illness) who responded to a Swedish web-based questionnaire at two time points. Using a confirmatory factor analysis, we calculated latent factor scores for 9 constructs, based on 34 questionnaire items. In this dataset, we share the latent factor scores and the latent profile analysis results. Although raw data are not shared, we provide the questionnaire item, including response scales. The code that was used to produce the latent factor scores and latent profile analysis results is also provided.
The study was performed as part of a research project exploring how the use of eHealth services in chronic care influence interaction and collaboration between patients and healthcare. The purpose of the study was to ide
Language
English
Swedish
Research principal
Responsible department/unit
Department of Learning, Informatics, Management and Ethics
Data contains personal data
No
Ethics Review
Swedish Ethical Review Authority - Ref. 2018/625-31/5 and 2018/1717-32
Unit of analysis
Population
Primary care patients with any of the following diagnoses: hypertension, heart failure, mental illness
Time Method
Study design
Observational study
Description of study design
Two-wave longitudinal questionnaire study set in a primary health care center in Sweden.
Sampling procedure
Time period(s) investigated
2018-10 – 2019-06
Geographic spread
Geographic location: Stockholm County
Geographic description: The study population consisted of patients from one primary care center in Stockholm Region.
Research area
Health care services and policies, General health and well-being
(CESSDA Topic Classification)
Health Care Service and Management, Health Policy and Services and Health Economy, Other Health Sciences
(The Swedish standard of fields of research 2011)
Carolina Wannheden, Marta A. Roczniewska, Henna Hasson, Klas Karlgren, and Ulrica Von Thiele Schwarz, 2022. Better self-care through co-care? A latent profile analysis of primary care patients’ experiences of e-health–supported chronic care management, Front. Public Health, Sec. Public Health Education and Promotion, accepted. doi: 10.3389/fpubh.2022.960383
DOI:
https://doi.org/10.3389/fpubh.2022.960383
von Thiele Schwarz, U., Roczniewska, M., Pukk Härenstam, K., Karlgren, K., Hasson, H., Menczel, S., & Wannheden, C. (2021). The work of having a chronic condition : development and psychometric evaluationof the distribution of co-care activities(DoCCA) scale. In BMC Health Services Research (Vol. 21, Issue 480). https://doi.org/10.1186/s12913-021-06455-8
DOI:
https://doi.org/10.1186/s12913-021-06455-8
URN:
urn:nbn:se:mdh:diva-56003
If you have published anything based on these data, please notify us with a reference to your publication(s). If you are responsible for the catalogue entry, you can update the metadata/data description in DORIS.
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Description
The DATASET consists of two files: factorscores_docca.csv and latent-profile-analysis-results_docca.csv.
* factorscores_docca.csv: This file contains 18 variables (columns) and 180 cases (rows). The variables represent latent factors (measured at two time points, T1 and T2) and the values are latent factor scores. The questionnaire data that were used to produce the latent factor scores consist of 20 items that measure experiences of collaboration with healthcare, based on the DoCCA scale. The
Version 1
https://doi.org/10.48723/kzja-5k21
Citation
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Data format / data structure
Numeric
Creator/Principal investigator(s)
Carolina Wannheden
- Karolinska Institutet, Department of Learning, Informatics, Management and Ethics (LIME)
Marta Roczniewska
- Karolinska Institutet, Department of Learning, Informatics, Management and Ethics (LIME)
Henna Hasson
- Karolinska Institutet, Department of Learning, Informatics, Management and Ethics (LIME)
Klas Karlgren
- Karolinska Institutet, Department of Learning, Informatics, Management and Ethics (LIME)
Ulrica von Thiele Schwarz
- Karolinska Institutet, Department of Learning, Informatics, Management and Ethics (LIME)
Time period(s) investigated
2018-10 – 2019-06
Variables
31
Number of individuals/objects
180
Response rate/participation rate
55%
A total of 308 participants were invited. Response rate at T1: 55%; Response rate at T2: 41%.